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This paper draws on the experience of one research project in action. It questions the lack of emphasis in research ethics codes on the competence and capacity of agencies when commissioning and sponsoring research. Different theoretical understandings and ethical models are drawn upon to explore how a research team translated ethical research in theory into ethical research in practice.
This paper draws on the experience of one research project in action. It questions the lack of emphasis in research ethics codes on the competence and capacity of agencies when commissioning and sponsoring research. Different theoretical understandings and ethical models are drawn upon to explore how a research team translated ethical research in theory into ethical research in practice.
This paper draws on the experience of one research project in action. It questions the lack of emphasis in research ethics codes on the competence and capacity of agencies when commissioning and sponsoring research. Different theoretical understandings and ethical models are drawn upon to explore how a research team translated ethical research in theory into ethical research in practice.
Michael Preston-Shoot, Veronica Wigley, Isabella McMurray and Helen Connolly This paper draws on the experience of one research project in action to evaluate the usefulness of research ethics frameworks when the environment surrounding project negotiation, data collection and dissemination is seriously disturbed by critical incidents. The paper questions the lack of emphasis in research ethics codes on the competence and capacity of agencies when commissioning and sponsoring research. Using events that surrounded one project, the paper researches the research. It explores what impacted on the creation of the context for ethical and effective research and how the researchers responded to the ethical challenges that emerged. Different theoretical understandings and ethical models are drawn upon to explore how a research team translated ethical research in theory into ethical research in practice within an organiza- tion in turmoil. Keywords Research Ethics; Duty of Care; Situation Ethics; Research in Action Introduction Contemporary concern with promoting good research practice, enhancing ethical awareness and profiling accountability focuses predominantly on what factors should be considered and what arrangements should be instituted before projects commence. For this purpose, and when identifying and responding to factors that obstruct such expectations, ethical guidelines are designed to enable individual research judgements to be informed by shared values and experience, and to be underpinned by widely held principles (SRA 2003). This paper, on the other hand, explores a series of interrelated dilemmas that arose after ethical approval had been obtained, monitoring arrangements put in place and data collection begun. It is grounded in the real world of agencies and ISSN 1749-6535 print/1749-6543 online/08/020150-22 2008 Taylor & Francis DOI: 10.1080/17496530802117581 Professor Michael Preston-Shoot is Dean of the Faculty of Health and Social Sciences, University of Bedfordshire, UK, Veronica Wigley is an independent research consultant based in Sheffield, UK, Isabella McMurray is a researcher in the Division of Psychology, University of Bedfordshire, UK, and Helen Connolly is a PhD student in the Department of Applied Social Studies, University of Bedfordshire, UK. Correspondence to: Michael Preston-Shoot, University of Bedfordshire, Faculty of Health and Social Sciences, Park Square, Luton, LU1 3JU. E-mail: michael.preston-shoot@beds.ac.uk ETHICS AND SOCIAL WELFARE VOLUME 2 NUMBER 2 (JULY 2008) practice, which perhaps offers a more solid foundation for the discussion of research ethics in action. The purpose is to contribute to debates about research ethics and governance, and to improve ethical literacy, especially within agencies that commission or sponsor research and within higher education institutions that must increasingly ensure ethical practice. Additionally, it suggests that preoccupation with ethical questions whilst research projects are being configured mistakenly sidelines the imperative of enhancing research quality across the entire process. Indeed, recorded experiences, and the insights they generate, may help to ground research ethics and to render them less abstract and more practical (Alderson & Morrow 2006). Question Definition For researchers and managers to understand and apply standards, principles and requirements of research governance correctly, they depend on a quality research culture that promotes excellence and is facilitated by strong research leadership (DH 2005) including within agencies that sponsor research. The ethical issues addressed in this paper are twofold. What if clear and supportive management arrangements in the field are not present or break down? How should researchers respond when an environment no longer exists wherein all parties can address openly and constructively issues derived from participating in research? Ethical Guidance Policy pronouncements on research ethics focus predominantly on the proposals and behaviours of researchers and the safeguarding of research participants. Thus, appraisal of social care proposals should include the competence of researchers, the nature of the data sought, the appropriateness of proposed collection methods and the utility of the research. This appraisal embraces the privacy offered to participants and the relationship between the researchers and those actively involved in the research, and the degree to which researchers have considered and addressed the likelihood of harm to participants (DH 2004). The Economic and Social Research Councils core principles (2005) include the integrity and quality of the research, informed consent and voluntary participa- tion, data confidentiality, storing of data and avoiding harm to participants, with limited discussion afforded to the period after the research in the form of dissemination of the findings. The Social Research Association (2003) and the British Psychological Society (2006) have issued similar guidelines. The focus is squarely on the risks to service users of poorly conducted research, and on the knowledge and skills of the researchers, with parallels to human rights as codified in European and UN conventions. These research frameworks sideline ETHICAL RESEARCH IN ACTION 151 any question of the competence of agencies both to commission and sponsor research or to act lawfully and ethically in respect of service users and staff. Some guidelines do spotlight the relationship between researchers and funders, seeing this as the key location for responsibility for ethical awareness (SRA 2003). Both the SRA (2003) and the Department of Health (2005) emphasize the need for a co-operative relationship wherein responsibilities are clearly allocated for the maintenance of standards, the safeguarding of ethics and the implementation of the research in a conducive atmosphere. The BPS (2006) recognizes that ethical quandaries do occur in the research process. However, once again the focus within this emphasis is telling. In the BPS guidance (2006) it is the psychologist researcher who has responsibility for the resolution of such dilemmas. The identification of responsibility for sponsors, to ensure arrange- ments for managing and monitoring research (DH 2005), highlights the research- ers practice rather than agency location and the availability of leadership and appreciation of research practice within it. The dominant concern appears to be quality control and assurance of the work of the researchers; the agency context is assumed to be benign and unproblematic. Thus, the SRAs guidelines (2003) bemoan the absence of a comprehensive system of registration in order to ensure researcher quality. This emphasis is further reflected in a taxonomy of research misconduct (Smith 2000) and in the guidance relating to research misconduct produced by some universities for their own staff. When guidelines refer to safeguarding participants dignity, well-being and safety (DH 2005), those principally in mind are service users rather than social (care) workers; when they refer to people having appropriate qualifications, skills and experience, the spotlight is on researchers but social work practitioners and managers may not have the experience and expertise to maintain a suitable environment for research to be undertaken and to enable dependable outcomes to be delivered. Similarly, the code adumbrated by Butler (2002) contains no reference to the responsibilities of research commissioners or hosts. The close proximity of social work research to social work practice does, however, lead to a suggestion that the ethical code for researchers should parallel that for social work more generally, implying that all stakeholders should be bound by ethical frameworks that are explicit and compatible. Professional codes of ethics, such as those published by the British Association of Social Workers (2003) and the International Federation of Social Workers (2004), identify social works core values of service and promoting social justice, the dignity and worth of the person, and the importance of human relationships, integrity, and competence. This explicit underpinning of values, aligned to human rights conventions, includes an obligation to contribute to social planning and to promote public participation in the development and evaluation of social services, work which may include research, alongside being able to account for the ethics of their practice. The international code (IFSW 2004) does not specifically provide guidance regarding research but acknowledges that more specific ethical codes of practice are available at national level. The BASW code (2003) contains specific ethical guidance for social workers when engaged in 152 PRESTON-SHOOT ET AL. research. The emphasis is principally upon the avoidance of harm to, and empowering and promoting the welfare of, participants. Once again, that researchers must be technically competent is stressed but on this occasion there is implicit recognition that the working context may not be entirely benign. Social workers are urged to uphold the code of ethics even though their employers policies may not be compatible with its provisions. For maintaining professional standards and ethical positions, codes and guidance utilize core principles: respect for autonomy, beneficence, non- maleficence and justice. This approach has been criticized for lacking founda- tional theory, obstructing ethical enquiry, being Western dominated, and promoting an individualistic bias (Israel & Hay 2006). Hardwick and Hardwick (2007), however, suggest that situation ethics, with its emphasis upon the contingent rather than the categorical nature of moral response, offers a useful basis for the ethical review of social care research because the uniqueness of contexts and the moral choices faced by researchers cannot be translated easily into principles. This does not mean that situation ethicists are not informed by any fundamental principles at all. Indeed, they acknowledge the need for human conduct to be guided (as opposed to bound) by the principles embodied within the collective moral system. However, at the core of their philosophy is the belief that harnessing human action to any fixed body of moral precepts rather than personal acumen can potentially serve to undermine the uniqueness of a situation, the choices surrounding it and, ultimately, the best interests of those involved. One such unique situation, and the choices surrounding it, forms the springboard for this paper. Literature Survey The social care research literature is not exactly replete with examples of complex practical problems with ethical implications arising during research projects. Israel and Hay (2006) do, however, give examples of difficult ethical problems encountered by social scientists. This has been attributed to gate- keeping by journal editors and researchers, both of whom prefer to publish successfully concluded designs (Alderson & Morrow 2006; Shaw & Norton 2007), and to the uncomfortable nature of discussing research difficulties and disappointments (OConnor 1992; Grinyer 2001). There has, however, been a longstanding critical evaluation of the experience of researching in feminist research in general and in ethnography in particular. Stacey (1988), for example, talks about the ethical difficulties of managing relationships in the field: . . . fieldwork represents an intrusion and intervention into a system of relation- ships, a system of relationships that the researcher is far freer than the researched to leave. The inequality and potential treacherousness of this relationship seems inescapable. (p. 21) ETHICAL RESEARCH IN ACTION 153 This experience resonates with some of the difficulties shared, if not reported, by social care researchers working closely with professionals in Britain. There has been some concern about the lack of information about how difficult ethical decisions have been made in the course of research projects. Burke (2007), in response to a perceived lack of detailed discussion of ethical issues in qualitative research in social work, both describes her own experiences and makes a plea for the allocation of more space by editors for such discussion in academic papers. Similarly, Dickson-Swift et al. (2007) draw attention to the lack of research on the effects of doing qualitative research on researchers, but again the focus is on reflections on their own experience rather than on the relationship between the host agency or institution and staff or service users. Other exceptions are papers by Grinyer (2001) and by Gallagher et al. (1995), both of which explore dilemmas when actually undertaking research that has been ethically approved. The authors are sanguine about the helpfulness of the advice that may be gleaned from ethical guidelines about how to deal with particular issues and choice points in research. Each offers some approaches or solutions for managing such issues as informed consent, the disclosure of confidential information and the handling of findings. Gallagher and colleagues (1995) refer to three approaches for managing ethical dilemmas. By expedient they mean adopting or adapting practical strategies that are likely to facilitate progress. By value driven they refer to individual researchers negotiating ethical dilemmas from their preferred orientation rather than from prescribed moral and philosophical frameworks. By pragmatic they mean resolving competing dilem- mas by employing a cost/benefit assessment that is intrinsically shaped by their personal value system. Their solutions include seeking advice from colleagues, using steering groups, and returning to ethics committees. For Grinyer (2001), the discretion left by ethical codes to individual researchers is a space that can be filled by training and by dialogue between the parties involved. Similarly, Hardwick and Hardwick (2007) advocate situation ethics because of the danger that procedural requirements will become givens and mean that the uniqueness of a situation will not be appreciated. They argue for an ethical review of research that reflects the complexities of the social world, human agency, and the realities of the individuals and groupings involved. For them, review relies on professional judgement and moral discernment, informed by the ethical maxims of the researchers. It might equally be influenced by other knowledge bases, such as service user views, research reports and theories capable of illuminating practice. Research Project Two of the authors had previously conducted research within this department (Preston-Shoot & Wigley 2005). This project was commissioned by a Social Services Department with the overarching aim of assessing outcomes for looked- after children. None of the researchers was employed by the department and 154 PRESTON-SHOOT ET AL. there were no other links, such as the provision of practice learning for students, between the department and the researchers university location. Three stages were envisaged for the project, each building on the information already gathered. Stage 1 would provide information regarding the different forms of residential care offered within the authority, the aims of different forms of provision and the extent to which they were meeting the needs of children and young people in their care. The next two stages were conceived as a longitudinal multiple case study design over a five-year period. Stage 2 would identify baseline measures, the prevalence of risk factors and the initial outcomes for children who became looked after in the course of this stage, coupled with outcomes for those who were at risk of becoming looked after but were currently living with their family. Importantly, it would also provide information about the perspectives of those involved, focusing mainly on children, parents and social workers but including foster parents and residential workers where appropriate. Stage 3 would evidence the longer term outcomes for the sample of young people engaged in stage 2, continuing to explore factors related to the social worker, residential worker, parents, and the child themselves, and the settings in which the young people lived, in order to see how these influenced the outcomes for the children or young people. Ethical approval was given by the University of Bedfordshires Institute of Applied Social Research and by senior managers in the organization sponsoring the research. A steering group, comprising senior managers, social workers, foster carers, residential workers and managers, and looked-after young people, met throughout the project and routinely focused on ethical issues, such as preserving confidentiality for participants when presenting reports and obtaining informed consent from young people and parents when describing research objectives. Stage 1 was concluded successfully. It used qualitative methods, augmented by data derived from standardized questionnaires to gather information about young peoples behaviour and emotional state. Information was gathered from 22 young people, care staff and managers in residential homes, and from social workers. At the beginning of stage 2 social workers were asked to examine their case lists and identify children and young people whom they perceived as being at risk of becoming looked after. Social workers were provided with a list of risk factors aggregated from child protection literature (Powell 2003; Preston-Shoot 2003) as well as being invited to add children they felt were likely to become looked after but who did not meet any of the criteria listed. They were asked to identify risk factors for these additional children. After consultation with social workers it was decided that some children should not be interviewed as it might be detrimental to their well-being. Although the final sample was selected through an informal assessment of being at risk of becoming looked after, it was representative of the departments overall work with children in need and children requiring protection in terms of age and gender. Outcomes were broadly defined as those set out in the Framework for the Assessment of Children in Need and their Families (DH 2000). Using this assessment framework as a platform for discussion, semi-structured interviews ETHICAL RESEARCH IN ACTION 155 were conducted with 32 social workers. These interviews were designed to gather information about and understand the holistic well-being of this purposive sample of 52 children (31 males and 21 females, aged between 0 and 16) who were looked after or at risk of becoming looked after. Various standardized measures were also used to gauge perceptions of a young persons strengths and difficulties, well-being, self-esteem, locus of control and self-efficacy. The processes that are analysed below occurred during stage 2 and resulted in the project being halted during data collection for that stage. Although anticipated as a short-term measure, in fact the project has not recommenced as the department has engaged in a major review of its child care policies, procedures and practices, led by newly appointed senior managers. Creating the Context for Ethical Research The focus of ethical guidelines for researchers quite reasonably draws attention to their reasons for undertaking particular projects. Some motivations may revolve around a desire to empower service users and to improve services by providing useful findings; others may centre on pursuing particular lines of enquiry, achieving personal and/or professional development, or contributing to a university departments research rating. Purposes may be concerned with effecting change and/or knowledge production, and focused upon clinical work or the experiences of those receiving services (Glasby & Beresford 2006; Oliver 1999). Faulkner (2004) consulted mental health service users and survivors in order to develop ethical guidelines for research carried out by or with them, but describes the guidelines as useful for research involving service users in general. Participants in the research concurred with suggested widely accepted principles but also added that a commitment to change was a critical element of ethical research. All this points to the importance of researchers understanding their context, and their own place within it (McAdam & Lang 1994), especially the kinds of influences that context exerts. However, if research is to be ethical, the commissioners reasons for supporting particular projects must be valid ethically, as must the context in which the research is undertaken. Some social care research may be commis- sioned in order to use the findings to improve services; in other instances, however, the motivation may be to provide a rationale to delay decision making or to justify a proposed policy shift. Indeed, the aims and aspirations of commissioning agencies may not always be made explicit (Shaw & Norton 2007). Nor might the contextual factors likely to affect data collection and implemen- tation of the findings*/political, organizational, structural, financial and rela- tional (Matland 1995)*/be fully understood or considered. Thus, ethically literate researchers might seek to understand how a research request fits with an agencys tasks, context and the services it offers (McAdam & Lang 1994), and to question whether an operational rather than a research response might be more appropriate. 156 PRESTON-SHOOT ET AL. Perhaps crucial for ethical research is what happens at the researcher/ commissioner interface. Humphries (2007) draws attention to the danger of social work researchers becoming enslaved by the demands of their paymasters. Compromises in research design may be negotiated or, indeed, imposed by sponsors because of timeframes for data availability, levels of accessible funding, and directed objectives or structures into which the researchers have to fit (Lloyd et al. 1996; Braye & Preston-Shoot 2005). Drawing on principles of systemic practice with families and organizations (McAdam & Lang 1994), researchers might usefully respond to requests by giving close attention to how they themselves are perceived, to the stories and events, ideas and beliefs that have led to their being commissioned. This research team was already well known to the commissioning agency, such that it might have been trusted with a troubling, even painful, brief, or perceived as likely to be less directly confrontative. Equally, researchers will frequently be working within councils with social services responsibilities whose track record of acting lawfully and/or unethically is highly variable, judging by judicial review outcomes, health and safety at work case law and reports from the Commissioner for Local Administration. These are also the contexts where research indicates that managers and practitioners may collude in respect of unacceptable service provision (Machin 1998; Horwath 2000). Such contexts reinforce the importance of seeking to understand, rather than draw a veil across, the research setting and, therefore, the rationale for conducting a particular project at a given time. However, although recognizing that relationships are pivotal to effective and successful research outcomes (Israel & Hay 2006), in this project the researchers initially accepted the commissioning agencys stated goal. This was to use data on the outcomes for looked-after young people to reconfigure the balance of settings in which care was provided, rather than to interrogate how managers and practitioners in that agency, together with residential and foster care providers, appreciated the context in which they were working. In common with other projects (Braye & Preston-Shoot 2005; France 1996), discussions on the research brief centred on safer dilemmas, such as timeframes and methodolo- gical debates, and took place within the commissioner system rather than across all the levels and with stakeholders within and beyond the funding agency. Positions and perspectives were not entirely unknown in this example. The researchers knew how some senior managers viewed strengths and weaknesses within child care teams and services for looked-after children. Indeed, the researchers had previously been critical of the standards of social work practice in the same agency (Preston-Shoot 2003). However, whilst this might have triggered further cautious reflection within the research team and between it and the agency within which they were working, it did not appear to question the integrity of the project at this point. Equally, as stage 2 was being negotiated, the commissioning agency had already used stage 1 findings in contractual negotiations about the future shape, provision and delivery of residential care services. Stage 1 had concluded that looked-after young people received good ETHICAL RESEARCH IN ACTION 157 physical care but variable responses to their emotional needs. The interface between social services and both education and housing required urgent attention at strategic management and operational levels. There was a lack of clarity about role expectations and role requirements at all levels, especially in relation to assessment and decision making, care planning and recording. There was a lack of information in social services systems about peoples needs, with additionally significant gaps in service provision and shortcomings in planning for young people and levels of partnership. The researchers also knew that some social workers were cynical about the likely impact on resources of the research and about the use by managers of consultants and researchers. To some degree the researchers shared such scepticism, having been concerned historically about the degree to which findings had been used or shelved. Nonetheless, the researchers did not follow advice (Grinyer 2001; McAdam & Lang 1994), namely to understand how research is perceived by all those involved. The researchers did not explore how perspectives about child care provision or the proposed research played out within the commissioning agency, nor indeed how low morale had become in parts of it, nor what the impact had been in terms of relationships of the contractual changes made in contracts for the provision of residential care. Why, then, at the point of research negotiation did the researchers not discuss the commissioning agencys commitment and ability to act on the evidence obtained? Whilst agreeing with the commissioning agency the content or task of the project at stage 2, what took the researchers away from a position of curiosity (Cecchin 1987) or space for reflective consciousness (Hardwick & Hardwick 2007)? This would have encouraged self-reflexive analysis in terms of what was happening to the researchers, and relational-reflexive analysis in terms of how the participants could develop and use the opportunities provided by the research to engage with each other to explore ways in which they were relating and to elaborate the potential in their working together. At least part of the answer lies in the context for and dynamics surrounding this particular project. Secrets Systemically, a secret in a family and/or professional system is something that everyone knows but nobody is allowed to discuss. The secret, which it is not open to people to explore, may be particular beliefs or the way people behave and the problems they have developed in the context of people and things around them (Stratton et al. 1990). At least four secrets were operating in the context surrounding this project. One was the authoritys geographical context, and the insularity this created. The impact on child protection systems of insularity has been noted (SWIA 2005). The pool of professional expertise may be smaller, especially as resources may be limited and complex cases not routinely encountered, and training opportunities may be more limited. Furthermore, recruiting high-calibre staff can also be problematic. Moreover, staff work closer 158 PRESTON-SHOOT ET AL. to communities in respect of whose members they may have to take unpopular or difficult decisions. As recommended in the SWIA report, this authority had engaged several consultants and research teams but effecting change was not straightforward. The second secret was the degree to which the senior management team in the commissioning agency had the change leadership skills necessary. These are the different attributes required in order to manage the diverse tasks and processes involved in managing change. Personal communication with members of the team indicated strengths in initiating ideas and work but weaknesses in keeping track of progress, monitoring and responding to the emotional climate, and completing tasks. The third secret was the lack of corporate responsibility within the authority as a whole for the well-being of young people and adults requiring care and services as a result of being in need or concerns about protection. The interface between social services and other departments within the authority had been raised both in stage 1 and in the planning of stage 2, and in earlier research but, as the research had been commissioned by social work managers, the researchers did not have direct access to other departmental managers or with political decision makers and could only suggest data collection and dissemination methods that would involve them. The fourth secret was an ongoing inquiry into the policies, procedures and practices surrounding an incident which was widely expected to be exceedingly critical of the standards of child care social work within the organization. Whilst outwardly the agency presented as business as usual, such that its functioning appeared stable, behind the surface lay internal intra-personal distress and anxiety, and inter-personal tensions. In order to avoid difficult emotions and behaviours these secrets were not confronted openly but were regulated instead through the use of distance regulators (Stratton et al. 1990). For example, the layout of the spaces occupied by managers and different social work teams made face-to-face communication difficult. Senior managers in social services controlled the boundary between themselves and the wider authority of which they were a part, meaning that the researchers had very few opportunities in which to use research findings to challenge the degree of expressed system corporateness for young people and their families. The Referring Person A research referral may be motivated as much by the desire to avoid anxiety and to maintain a professional position as to achieve change. The referrers objective may be to take the heat out of problematic relationships by calling in an expert who is invited to move between the referrer and the other participants, such that direct communication between members of this dyad is instead detoured through the researchers. Effectively the system remains ETHICAL RESEARCH IN ACTION 159 unchanged. This suggests a focus for researchers on the position of the referrer in the system being presented as the research location, and on interactions within and between organizational systems in order to avoid becoming triangulated or incorporated into an agencys relationship patterns (Preston-Shoot & Agass 1990). This interactional focus, especially where all participants are brought together, allows researchers to avoid the pitfalls of becoming enmeshed in secrets and alliances. Enmeshment means a loss of leverage because researchers become associated or allied with one aspect of a dyad, namely the commis- sioners, rather than facilitating dialogue between them and others, in this instance social workers or senior managers in other departments of the agency. It allows researchers to address relationships and interactions surrounding the referral, and to ask questions that will answer whether or not research is contraindicated, perhaps because everyone engaged does not have the con- fidence or capacity to deal with ethical matters or to manage matters ethically (Girling 2007). There are key questions (Stratton et al. 1990; McAdam & Lang 1994) when convening the system. What is the context? What is the problem? Why is it a problem now and who is it a problem for? At what point did the research idea emerge? Who else should be involved? What is the position of everyone in this system of concern and what solutions would assist the position they start from? In this project, the failure to convene the organizational system at the outset allowed some people to disengage and probably reinforced resistance to, or scepticism about, the research. This was not just because, as often lies behind research fatigue, it was seen as a distraction from practice and unlikely to have a noticeable impact on service provision (Harrison 1999). It was also because research was viewed as an external imposition, greeted with apathy or anxiety which, in the context of unexplored secrets and relationships within the commissioning agency, was left uncontained (Obholzer & Zagier Roberts 1994) and also because the research engaged with only one definition of the problem. Additionally, and especially reinforced in the context of the ongoing inquiry, the research request moved individual and organizational practice from the private to the public realm, besides being an exercise of power in describing the problem or concern in a particular way and locating it in particular systems (the appropriateness of types of residential care and the thoroughness of social workers assessments, for instance). If unaddressed, research may trigger both anxiety and resistance. It may reinforce the taking of positions rather than moving beyond how problems are presented, even pathologized (McAdam & Lang 1994), towards a space where a more consensual, co-operative domain may emerge. Put another way, experience in this project highlights the significance of continual scrutiny of triangular relationships, and the way research sets up or reinforces existing relationships. Some social workers were already wary of talking to managers or of being openly critical of the organization. Since the researchers talked only with senior managers when agreeing the specification for the research, rather than negotiating more broadly, this arguably accentuated 160 PRESTON-SHOOT ET AL. wariness. As some social workers then distanced themselves and the looked-after young people on their caseloads from the research, for example by cancelling booked interview appointments, the researchers became aligned even more closely with the commissioning managers in attempting to enforce co-operation. The anxiety then passed around the organization was that relating to their unfulfilled expectations of the research, leaving the internal state of individuals and systems untouched. A vicious circle was therefore created (Preston-Shoot & Agass 1990), with several increasingly forthright attempts by managers to secure some social workers participation in the research. This represented a more of the same intervention rather than a stepping back to consider distancing as information, as a reasonable response to a perceived unreasonable situation. This illustrates that who is engaged when the research is being proposed will influence how the problem is constructed and whose needs are (perceived to be) met (Humphries 2007). Uncontained Disturbance Increasingly, as data collection in stage 2 progressed, it became apparent just how stressed and defensive some social workers felt, and how potentially dangerous some practice was. There was a clear lack of trust and an experienced absence of support between practitioners and managers, and no sense of the containment necessary (Obholzer & Zagier Roberts 1994) to enable practitioners to engage with the emotions, dilemmas and complex relationships encountered within child care and child protection. Social workers felt unsafe, describing how the organizations priorities were changed weekly and how managers were not questioning decisions but were making decisions more because of what they would look like in public than based on child-protection issues. They increasingly spent much of the interview space discussing adversities in the work environ- ment, describing the authority as having an atmosphere of mistrust, so much so that some social workers made notes of all discussions they had with colleagues. The mood and malaise is captured by the following extract from one research interview with a social worker: You want the truth . . . I have had supervision once since I have been here . . . I am a newly qualified social worker and I have only had supervision once in 3 months and in my opinion is unacceptable . . . I have been thrown in the deep end and left to swim . . . I do not know what decisions are mine to make and what arent . . . They [the managers] would not want to hear the truth anyway so I wouldnt tell it to them. You know it is very odd here. You have to be very careful . . . It is the old school, who you are friends with . . . It is really weird. There is an undercurrent of, be careful who you talk to and it will get back . . . We just lost a social worker yesterday because she was like this is too dangerous here . . . Everyone is scared. The management are scared and you can feel it. The environment had elements of what one judge, when quashing a local authoritys care plan in respect of a disabled young person (R on the application ETHICAL RESEARCH IN ACTION 161 of CD (a child by her litigation friend VD) v. Isle of Anglesey CC [2004] 7 CCLR 589), compared to a computer virus, a demon that had affected local authority decision making. What was emerging through meetings with social workers was clear evidence of a loss of personhood when institutions subvert professional judgements (Dombeck & Olsan 2007) and of the depersonalizing effects of an institution because of the breakdown of containing and reflective mechanisms such as supervision where individual and organizational internal states could be held and discussed. The earlier quotation provides one illustration. Below is another: One of the cases I have concerns . . . the decisions made in a child protection conference were overturned, the three to five or six decisions that we all agreed . . . but as soon as the mother started kicking up, its like no, just give in, so the decisions I made have been overturned. So, I dont have any control over this situation . . . I couldnt say to my supervisor, I am feeling unsupported. Why did you do that to me? I couldnt do that, I was saying everything its fine . . . because who shes friends with . . . When something happens here, people are afraid of everything, so it is cover your own back . . . I know like I feel unsafe because I know if something goes wrong, I will be blamed. These quotations raise a question about the degree to which informed consent in the choice of cases where there is a sample was prejudiced in this instance. Social workers had no say in which cases they would be asked to discuss as the researchers selected the sample, albeit from data provided by social workers where they were able to select from amongst their cases those young people they believed to be at risk of becoming looked after by the authority. Social workers may be comfortable and give consent to discussing a case where they feel that practice was good but may feel less comfortable when they have concerns about how work on the case was conducted. If social workers are to give informed consent, should they know which cases are to be discussed before consent is given? Furthermore, to ask professionals to identify how, when and why specific decisions were made exposes their practice to their own reflective thinking and also to questioning and evaluation by others, including the researchers and those who read project reports. That this will happen in the processes underpinning this type of research is inevitable but the extent to which it will happen, and the stress that this might occasion, may not be recognized by social workers. Exposing staff to stress while researching practice, whether or not this can be recognized by them beforehand, may be justified by researchers in terms of potential gains for, as here, looked-after children. However, if research proceeds when participants may not be fully aware of the stress that involvement may cause them, there are additional obligations on researchers. This is because respondents are exposing their perceived lack of safety within the organization whose responsiveness in management of practice, and implicitly therefore their likely reply to research findings, is being criticized. Questions, therefore, began to emerge surrounding the integrity and viability of the research. 162 PRESTON-SHOOT ET AL. When is a Research Space Not a Research Space? The quotations illustrate a subtle shift that meant at least some research interviews came to resemble supervision sessions. The opportunity to talk to the researchers about a case in depth and confidentially was valued explicitly by many participants but the time this took had to be weighed against the case work that could have been done in that time. Given the nature of their work, this was a very real concern for several participants. Both the researchers and managers justified this use of time in terms of the greater good, or beneficence (Butler 2002)*/improvements to services for looked-after children and individual practice. Such justifications relied on optimistic assumptions that the findings of the research, including understanding that emerged from within these interviews, would be both relevant to practice, which was a fundamental concern for the researchers, and would be used to develop services. However, the researchers had no control over the formulation or enactment of policy changes made as a result of research findings, and limited opportunity to check back with participants on the use they had made in practice of insights derived from the interviews. A related question revolved around the validity of the data obtained in these interviews. The extent to which it was legitimate to use these data, the degree to which the focus of the study was changing, and even whether it was possible to maintain focus on the interview questions in the privileged situation of an encounter between a researcher and social worker (Grinyer 2001), exercised the researchers. Some of the research team felt that the data would have limited utility, as a result of the agency being distracted by organizational dysfunction and anticipating upheaval after conclusion of the inquiry. Others emphasized the social benefits of the research, if not immediately but as information to influence reorganization after the inquirys conclusion (cf. Gallagher et al. 1995). The potential benefits and hazards, including psychological and disclosure dangers, for both the social workers and the researchers from their participation emerged for consideration, for instance around how to protect confidentiality of respondents in such a small authority. Humphries (2007) refers to the tensions amongst stakeholders when they hold competing objectives, for instance about the use of findings to inform policy and practice. Here, the extent to which social workers were able to make an uncoerced choice about whether or not to participate in the research was affected by a number of issues. The research was commissioned by their employer and was presented as a critical plank in the development of services for young people. Social workers knew that not taking part would be seen as obstructive. The issue here is the extent to which an employer has the right to demand staff participation, and whether ethical research is prejudiced where participants feel that they have little choice about whether they engage. While it is clear that managers have a duty to provide services that are as good as possible, and therefore must have a duty to gather ETHICAL RESEARCH IN ACTION 163 information on which to base service provision decisions, the rights of staff are less clear and therefore the onus is the greater on researchers of non- maleficence, of avoiding harm (Butler 2002) in situations where the interests of managers and social workers do not coincide. Report or Action-oriented Research Social workers did not appear to have much faith in their managers, as the following quotation illustrates: I dont think managers at the basic level get to manage properly. They are not given the time, the opportunity to manage us . . . Anything that we seem to do is still crisis level. We cannot plan anything . . . They [first-line managers] are too integrated into the higher levels of management . . . their role [should be] more operational . . . The mandate from the commissioning agency was to provide information through a sequence of interim and final reports. The research was not conceived as an action research project and the researchers did not negotiate a mandate to work for organizational change. When faced with the extent of disillusionment within the organization, the question facing the researchers was whether, and if so how, to act either as emissaries for the research participants to the commissioners (Grinyer 2001) or as mediators in this dyad. The researchers wanted the voice of young people and their parents to be heard. However, they were uncertain of the degree to which their responsibility included connecting people to their organizations (Dombeck & Olsan 2007) so that problems could be aired, and doubted their ability to use the research as an opportunity to engage in social change in this institution, partly because of how the research had been established and partly because of the pain and anxiety that existed at different levels within the agency. Moreover, maintaining confidentiality and ensuring that participants could not be identified (unless they gave prior permission) in written and/or verbal reports was a fundamental ethical commitment made to participants. While this poses few problems in academic publications, it does create difficulties in research carried out and reported to one department. Where people know each other well it can be difficult to anonymize data sufficiently for such data to be unattributable. Yet omitting these data might reduce the value of the research to commissioners and, ultimately, to client groups. The researchers used a steering group, which included social workers and service users, to advise on whether cases and/or workers might be identifiable in draft reports, but this in itself constituted a breach of confidentiality if cases and/or staff were identifiable. 164 PRESTON-SHOOT ET AL. Finding the Edge of Practice Since the client group consisted of vulnerable children and their families, the commitment to confidentiality explicitly excluded any information provided about actions by social workers, which could place a child or family at significant risk of harm. While there was much good practice in the department, examples were not infrequent of lack of care and concern about young people and their families, lack of adequate records and inadequate professional knowledge and analysis of practice in relation to cases for which social workers were responsible. For example, one young person had a score on the adolescent well-being scale that was predictive of a depressive disorder but the social worker disregarded this finding, saying that the young person was seeking attention and had refused child and adolescent mental health services in the past. One young person referred to bullying by residential workers but did not want this information disclosed to social workers for fear that it would jeopardize plans for independent living. In another case, concerns arose about the likelihood of a young person abusing other children in different settings. One social worker refused to act on the basis that it was not their case; another did not include this information in a research interview but the residential worker did in the context of feeling unable to share the information with social services. Decisions were not easy in relation to the point at which poor practice puts children at such risk that confidentiality should be breached. The overriding reasons to disclose might not always be clear (Grinyer 2001). In practice the researchers relied on early reporting of anonymized failures to meet their ethical obligations, but was this good enough? In reality the researchers were working with a department under considerable strain and in retrospect (and even at the time) it seemed unlikely that positive actions would be taken to address the relationship, procedural and structural failures that were reported. Some members of the research team, from a utilitarian viewpoint, argued that continuing the research and not prejudicing the collaboration of the social worker participants would enable the project to provide data on which improvements to services for all children could be built. Others believed that the safe edge of practice had been crossed and that the department had become dangerous, such that disclosure to regulatory bodies should be made. To Research or Not to Research? The splits that emerged in the research team, around the validity of the data collected and ultimately the integrity of the project, mirrored the splits in the organization that had commissioned and hosted the research. Psychodynamic and systemic theories recognize that dysfunction in one system can evoke disturbance in another adjacent system, through a process known as re-enactment, mirroring or parallel process (Preston-Shoot & Agass 1990). The split based on this mirroring most clearly emerged when the researchers ETHICAL RESEARCH IN ACTION 165 discussed whether to terminate the project. Whilst the tangle was not fully appreciated at the time, and whilst it did not undermine the teams work, it was both a source of information about the agency where the research was located and about unresolved anxieties, needs, disappointments, and relationships in one or other, or both systems. Ending as Another Beginning Guidance (DH 2005) suggests that substantive changes to research projects should be submitted for ethical review and sponsors agreement. The commis- sioning agency, as represented by senior managers, did agree to the researchers proposal that the project be suspended. Moreover, it is arguable that the nature of the contract between the research team and the commissioning agency would have allowed the researchers to withdraw on the basis that the project was being frustrated. This is a term from contract law to recognize that problems may arise that cannot be eliminated and that render it impossible to complete the proposed work in a context where renewed planning is unlikely to resolve the outstanding concerns. However, deciding whether or not to continue or to withdraw from research, which is of potential benefit, is not straightforward because in itself it is an ethical issue (Gallagher et al. 1995). Not surprisingly, then, the research team remained divided even after the decision was made. Gaps in knowledge about outcomes and professional intervention, coupled with the objective of providing data to inform service improvement and the recognition of the vulnerability of looked-after young people, had to be balanced against the vulnerability of other respondents, especially social workers, and concerns about the safety of social work and research practice in this agency context. Ultimately, the researchers took the view that gaps in knowledge could be rectified more effectively once the organization commissioning the research was better able to move forward. Nonetheless, the way the contract was originally set up continued to create difficulties, leaving the researchers holding a conflict of interest between their obligations to participants and their sponsors. Different codes of conduct highlight the need for researchers to debrief or disseminate the findings of research to the participants (SRA 2003; BPS 2006). The research governance framework (DH 2005) also names as the sponsors responsibility the making of appropriate plans for the dissemination of research findings. However, the department did not initially release the reports prepared on stage 2 or respond to the researchers request for clarification about how and when the reports could be released, which was triggered by a request from one social worker and one service provider for further information on the findings. Equally, the researchers struggled with how to explain to participants the reasons behind their withdrawal, at least temporarily, when practitioners, managers and families must continue to work together. The question here is how to balance justice, or dealing fairly, with non-maleficence or the avoidance 166 PRESTON-SHOOT ET AL. of harm. This is similar to the ethical issue, again based on a concern about the potentially deleterious effects of disclosure on the relationships between families and social workers, of declaring explicitly and precisely all details of a research project when providing information. The researchers justified their decision to circulate a summary of the findings and to link postponement to the pending inquiry report, knowledge of which was widely known, by reference to the principle of avoiding harm, which fuller disclosure of the agency context was likely to cause. Concluding Discussion Hardwick and Hardwick (2007) suggest that situation ethics will illuminate an understanding of complex processes and allow for values to guide how a relationship of care should be expressed. They place considerable store on the researchers ethical maxims and on openness to listening to the situation as key signposts in searching for an appropriate response. However, ethical models and codifications of values differ within and across professions, such that how and when to intervene may not appear straightforward. Equally, as demonstrated in this paper, other sources of knowledge may prove helpful signposts. Gallagher and colleagues (1995) offer two suggestions to researchers for when research in practice becomes ethically complex. The first is referral back to a research ethics committee. This may provide an opportunity for critical reflection by virtue of the committees detachment. However, research govern- ance structures in the agency at the time of the project were limited and the project itself had received ethical approval through the universitys own structures and from senior managers in the organization hosting the research. Thus, referral back in this instance seemed to offer little. In practice, the outcome of any referral would also have been affected by two factors. Firstly, the degree to which any committee was risk averse, oriented towards minimizing organizational risk (Israel & Hay 2006). Secondly, by how procedural ethics, achieving sound processes at the outset, were balanced against ethics in practice, the complexity of issues surrounding participants in an organization in crisis. Outcomes would also be affected by the ethical literacy of the committee, and the ethical frameworks it privileged, which may or may not be transparent. Ethical committees with a member who is a professional ethicist are rare but including one could inform ethical decision making. Perhaps consulting an ethics committee on issues arising in the process of the research might be useful, if the emphasis is on consultation rather than giving the power to make a decision to the committee. As members of ethical committees are usually experienced researchers it is difficult to justify privileging their views where equally experienced researchers are doing the research. Their second suggestion is to utilize steering groups. The researchers had brought together a steering group for this project, comprising a senior manager, two social workers, a looked-after young person, foster carers, and residential ETHICAL RESEARCH IN ACTION 167 workers and managers. Looking at the composition of this group, to varying degrees members were part of the problematic dynamics about which the researchers had become increasingly concerned. Some issues were discussed in the group, such as how to ensure the safety of researchers when visiting participant families in their own homes, how to preserve confidentiality for participants in a small authority in reports prepared for the agency, and how to secure the co-operation of social workers. However, issues of trust in what the researchers came to see as an unsafe and conflicted environment, the possible impact of the inquiry findings, and the concerns about practice standards felt increasingly difficult to raise. Perhaps this was out of (misplaced) loyalty or protection to especially the senior manager and the social workers in the group. Perhaps it derived from the researchers increasing awareness of covert alliances and relationships in the agency. Perhaps there was a growing sense that key parts of the organization were not represented and thus the steering group did not have sufficient authority to intervene. Thus, the researchers decision to suspend the research and to withhold data dissemination until after the inquiry findings had been published and worked through was not shared with the group. As with Gallagher and colleagues (1995), ultimately pragmatic considerations, informed by a systemic and psychodynamic understanding of organizations in difficulty, guided the decision to suspend the project. Promoting the well-being of young people and their families by disseminating data about practice outcomes had to be weighed against the capacity of the sponsoring organization to make use of the findings at a time of crisis and the ability of the researchers to engage all the participants sufficiently to ensure the integrity of the researchs design. Ethical codes and the researchers professional values, ethical research in theory, helped to shape understanding and action. The researchers sought to apply ethical principles in their management of day-to-day relationships with project participants, ethical research in practice. However, the crucial dilemmas for this project occupied a different space, ethical research in-between (Jenness & Grattet 2005). How ethical research theory, as embodied in codes and professional values, was translated into practice was worked through by drawing on experience and knowledge, and was affected by the growing appreciation of the environment in which the researchers found themselves. It was also affected by the perviousness of different layers in this organization and their susceptibility to engagement with ethical research, project objectives and critical perspec- tives on policy and practice. Arguably, codes are less helpful for ethics in- between, this space between theory and front-line practice, where maintaining sound processes and achieving successful outcomes confront responses to practice complexities. Put another way, codes fail to solve situational ethical issues in the field (Grinyer 2001). Social work research has the practice of social work as its operational domain (Butler 2002), with all its dilemmas and conflicting imperatives. This renders universal principles of limited value. Rather, it requires an ethical literacy which enables problem solving (Girling 2007) based on understanding, informed by an appreciation of what constitutes ethical research 168 PRESTON-SHOOT ET AL. and management of problems ethically, but developed and applied in a unique context. This is one aspect of the reflective researcher (Banks 2006), taking a critical stance towards practice via dialogue and questioning. This article has not discussed other ethical dilemmas which arose in this project and which frequently challenge researchers (see Gallagher et al. 1995), such as how to obtain informed consent from young people and parents, and what information to provide when seeking this consent about project focus and aims, which could be seen as casting doubt either on the ability of social services to safeguard and promote the welfare of children, or on the likelihood of families being able to respond appropriately to the needs of children. One aim here has been to explore a problem about which the research literature has been conspicuously silent but which judicial reviews, ombudsman investigations, and research and inquiry evidence (e.g. Horwath 2000; Machin 1998) continue to expose, namely unlawful and/or unethical and/or unprofessional relationships and practices. Another aim has been to focus on researching research as a source of learning. Ethical research is not just something on which to focus when seeking approval for a project (Israel & Hay 2006). Admittedly, greater attention should be paid when reviewing the fitness of the organization that is hosting the research and the contractual negotiations between all the parties. However, the essential message from the experience reported in this article is that greater attention needs to be given to how researchers behave after project approval and to how the ethical demands of research in-between, the translation of principles into a project, and then research in practice respond to the unfolding relational complexities. References Alderson, P. & Morrow, V. (2006) Multidisciplinary Research Ethics Review: Is it Feasible?, International Journal of Social Research Methodology, Vol. 9, no. 5, pp. 405/17. Banks, S. (2006) Ethics and Values in Social Work, 3rd edn, Palgrave, Basingstoke. Braye, S. & Preston-Shoot, M. (2005) Emerging Out of the Shadows? Service User and Carer Involvement in Systematic Review, Evidence and Policy, Vol. 1, no. 2, pp. 173/93. British Association of Social Workers (BASW) (2003) Code of Ethics for Social Work, BASW, Birmingham. British Psychological Society (BPS) (2006) Code of Ethics and Conduct, BPS, Leicester. Burke, T. (2007) Providing Ethics a Space on the Page: Social Work and Ethnography as a Case in Point, Qualitative Social Work, Vol. 6, no. 2, pp. 177/95. Butler, I. (2002) A Code of Ethics for Social Work and Social Care Research, British Journal of Social Work, Vol. 32, no. 2, pp. 239/48. Cecchin, G. (1987) Hypothesising, circularity and neutrality revisited: An Invitation to Curiosity, Family Process, Vol 26, no. 4, pp. 405/413. Department of Health (DH) (2000) Framework for the Assessment of Children in Need and their Families, The Stationery Ofce, London. Department of Health (DH) (2004) Research Governance Framework for Social Care: Guidance on Appraising Research Proposals, Department of Health, London. Department of Health (DH) (2005) Research Governance Framework for Health and Social Care, 2nd edn, Department of Health, London. ETHICAL RESEARCH IN ACTION 169 Dickson-Swift, V., James, E., Kippen, S. & Liamputtong, P. (2007) Doing Sensitive Research: What Challenges do Qualitative Researchers Face?, Qualitative Research, Vol. 7, no. 3, pp. 327/53. Dombeck, M. & Olsan, T. (2007) Ethics and the Social Responsibility of Institutions Regarding Resource Allocation in Health and Social Care: A US Perspective, in Ethics: Contemporary Challenges in Health and Social Care, eds A. Leathard & S. McLaren, Policy Press, Bristol. Economic and Social Research Council (ESRC) (2005) Research Ethics Framework, ESRC, Swindon. Faulkner, A. (2004) The Ethics of Survivor Research: Guidelines for the Ethical Conduct of Research Carried Out by Mental Health Service Users and Survivors, Policy Press, Bristol. France, A. (1996) Exploitation or Empowerment? Gaining Access to Young Peoples Reections on Crime Prevention Strategies, Groupwork, Vol. 9, no. 2, pp. 169/85. Gallagher, B., Creighton, S. & Gibbons, J. (1995) Ethical Dilemmas in Social Research: No Easy Solutions, British Journal of Social Work, Vol. 25, no. 3, pp. 295/311. Girling, J. (2007) Ethics and the Management of Health and Social Care, in Ethics: Contemporary Challenges in Health and Social Care, eds A. Leathard & S. McLaren, Policy Press, Bristol. Glasby, J. & Beresford, P. (2006) Who Knows Best? Evidence-based Practice and the Service User Contribution, Critical Social Policy, Vol. 26, no. 1, pp. 268/84. Grinyer, A. (2001) Ethical Dilemmas in Nonclinical Health Research from a UK Perspective, Nursing Ethics, Vol. 8, no. 2, pp. 123/32. Hardwick, L. & Hardwick, C. (2007) Social Work Research: Every Moment is a New and Shocking Valuation of All we Have Been, Qualitative Social Work, Vol. 6, no. 3, pp. 301/14. Harrison, M. (1999) A Social Action Approach to Research, in The Politics of Social Work Research and Evaluation, ed. B. Broad, Venture Press, Birmingham. Horwath, J. (2000) Child Care with Gloves On: Protecting Children and Young People in Residential Care, British Journal of Social Work, Vol. 30, no. 2, pp. 179/91. Humphries, B. (2007) Research Mindedness, in Social Work: A Companion to Learning, eds M. Lymbery & K. Postle, Sage, London. IFSW (2004) Ethics in Social Work: Statement of Principles, International Federation of Social Workers and International Association of Schools of Social Work, Bern. Israel, M. & Hay, I. (2006) Research Ethics for Social Scientists, Sage, London. Jenness, V. & Grattet, R. (2005) The Law-in-between: The Effects of Organisational Perviousness on the Policing of Hate Crime, Social Problems, Vol. 52, no. 3, pp. 337/59. Lloyd, M., Preston-Shoot, M., Temple, B. & with Wuu, R. (1996) Whose Project is it Anyway? Sharing and Shaping the Research and Development Agenda, Disability and Society, Vol. 11, no. 3, pp. 301/15. Machin, S. (1998) Swimming against the Tide: A Social Workers Experience of a Secure Hospital, in Whistleblowing in the Social Services: Public Accountability and Profes- sional Practice, ed. G. Hunt, Arnold, London. Matland, R. (1995) Synthesising the Implementation Literature, Journal of Public Administration Research and Theory, Vol. 5, no. 2, pp. 145/74. McAdam, E. & Lang, P.(1994) Referrals, Referrers and the System of Concern, unpublished paper, Kensington Consultation Centre, London. OConnor, I. (1992) Bereaved by Suicide: Setting up an Ideal Therapy Group in a Real World, Groupwork, Vol. 5, no. 3, pp. 74/86. Obholzer, A. & Zagier Roberts, V. (eds) (1994) The Unconscious at Work: Individual and Organisational Stress in the Human Services, Routledge, London. 170 PRESTON-SHOOT ET AL. Oliver, S. (1999) Users of Health Services: Following their Agenda, in Critical Issues in Social Research: Power and Prejudice, eds S. Hood, B. Mayall & S. Oliver, Open University Press, Buckingham. Powell, C. (2003) Early Indicators of Child Abuse and Neglect: A Multi-professional Delphi Study, Child Abuse Review, Vol. 12, pp. 25/40. Preston-Shoot, M. (2003) A Matter of Record?, Practice, Vol. 15, no. 3, pp. 31/50. Preston-Shoot, M. & Agass, D. (1990) Making Sense of Social Work: Psychodynamics, Systems and Practice, Macmillan, London. Preston-Shoot, M. & Wigley, V. (2005) Mapping the Needs of Children in Need, British Journal of Social Work, Vol. 35, no. 2, pp. 255/75. Shaw, I. & Norton, M. (2007) The Kinds and Quality of Social Work Research in UK Universities, Social Care Institute for Excellence, London. Smith, R. (2000) What is Research Misconduct?, in The COPE Report, pp. 7/11, Committee on Publication Ethics, London. Social Work Inspection Agency (SWIA) (2005) An Inspection into the Care and Protection of Children in Eilean Siar, Scottish Executive, Edinburgh. Social Research Association (SRA) (2003) Ethical Guidelines, SRA, London. Stacey, J. (1988) Can there be a Feminist Ethnography?, Womens Studies International Forum, Vol. 2, no. 1, pp. 21/27. Stratton, P., Preston-Shoot, M. & Hanks, H. (1990) Family Therapy: Training and Practice, Venture Press, Birmingham. ETHICAL RESEARCH IN ACTION 171