key: cord-0739029-67rnkl02 authors: Townsend, Ellen; Nielsen, Emma; Allister, Rosie; Cassidy, Sarah A title: Key ethical questions for research during the COVID-19 pandemic date: 2020-05-31 journal: The Lancet Psychiatry DOI: 10.1016/s2215-0366(20)30150-4 sha: fb8b254184e7e7b6768c2e5bf62fda21053765ea doc_id: 739029 cord_uid: 67rnkl02 nan and changes in the mental health system, both inside (ie, in the formal mental health system) and outside (ie, in the community), are necessary to bring about any improvement. EMHIP is a practical, locality-based service improvement programme designed to bring about this change. The aim of the project is to reduce ethnic inequalities in access, experience, and outcome within local mental health services. EMHIP will start with a process of knowledge and evidence synthesis, bringing together experiences of service users and individuals from BME communities, examples of good practice across the country, evidence in relation to equitable and effective mental health care, and research findings and recommendations from inquiries and reports. From this initiative, a practical, whole-system intervention programme will be developed and adapted for the purpose through a process of coproduction, involving service providers, service users, and BME communities locally. In phase 2 of the project, this intervention programme will be implemented in one borough (Wandsworth), and further refined by engagement and consultation with local communities and service users. Outcomes will be evaluated systematically through a cycle of comprehensive ethnicity audits based on routine service use data (adapted and augmented where necessary) and additional qualitative data. When other initiatives to improve mental health care for BME communities have failed to produce meaningful or sustainable change, 7 why should this project succeed? There are several reasons to believe that this approach will change the current, discriminatory dynamics of mental health care. EMHIP is a service-level intervention that is conceptualised, primarily, as a way of improving the overall quality of clinical care and patient safety for everyone, not just BME groups. The project combines an inside and outside approach through equal participation and commitment from statutory care providers, community agencies, and the wider community. The success of such a whole system project depends on strong leadership and collaboration between various key stakeholders. This process is underway in southwest London, where local BME communities and service users are "stepping up boldly" along with NHS agencies to ensure that local mental health services are respectful, effective, safe, and appropriate to their needs. 8 In these times of rapid change, with high levels of uncertainty, anxiety, social isolation, and financial pressure, mental health worldwide is likely to be at risk. Researchers are rightly ensuring that mental health research is included in the response to the coronavirus disease 2019 (COVID-19) pandemic. 1 Here, we reflect on ethical issues to consider when conducting research on self-harm, suicide, and the broader impacts of COVID-19 in the midst of a global pandemic, and provide some recommendations to consider when researching these topics. In non-pandemic times, research suggests that participating in self-harm and suicide studies is unlikely to cause substantial distress, even in the most vulnerable, 2 and that any detrimental effects are short lived and outweighed by altruism. 3 However, we do not know whether this holds in the context of a global pandemic. Researchers around the globe have paused their work for several reasons. First, to avoid unnecessary burden on people who might be in distress during the pandemic. Second, because the context of the current research environment means that results will require cautious interpretation. Third, to ensure that continued recruitment of people to studies on self-harm and suicide when a global crisis is occurring is reasonable and safe; transferring face-to-face research online must be very carefully considered. Finally, because the supports and services that participants would be signposted to throughout a study might not able to provide support in the usual ways and formats. Mental health research, including self-harm and suicide, is a vital part of the response to the pandemic, but we are concerned about the ethical robustness of some studies already recruiting. We have seen studies that do not provide sufficient information to enable fully informed consent, do not measure mood before or after participation, do not provide any signposting other than to potentially anxiety-provoking messages about COVID-19, and do not attempt any kind of mood mitigation or debrief to help to stabilise anyone that does become distressed after participation. We would recommend that researchers be mindful that general research into the impacts of COVID-19, even if this does not evaluate mental health, self-harm, or suicide, should be viewed as a highly sensitive topic, with similar attention to safeguards needed to protect the wellbeing of participants. We recommend that all studies into COVID-19, selfharm, and suicide measure mood before and after participation; a simple visual analogue scale has been used to good effect in several studies. 4 These mood measurements can also be used to decide whether a study can ethically continue, with a stop-study criterion set and applied if participants report very decreased mood after participation. Researchers should provide signposting and check that the services signposted to are operational and able to provide support (and in what format). Finally, providing mood mitigation to all participants is an important method to boost mood, particularly when participants have been asked to consider anxiety-provoking questions about COVID-19 and answer sensitive questions about selfharm or suicide. A number of methods including exam howlers, 5 cute animal pictures, 4 interactive websites, 6 and so-called doodle pages 7 have been shown to work for young people. The ethics of voucher lotteries and other incentives for participants in studies on suicide and self-harm have been questioned by lived experience authors. 8 Valuing the time of participants who contribute to these studies and respecting the challenges of taking part in research on difficult topics is important at a time of financial difficulty for many, particularly when there is little access to supports. For new work evaluating COVID-19 and mental health impacts, patient and public involvement must be central to prioritising and designing research studies. Indeed, the MQ COVID-19 and mental health initiative 1 includes people with lived experience in the 18 members of their leadership team. This would be strengthened if people with lived experience were among the core leadership team (currently comprised of six senior academics). More than ever, it is crucial that patient and public involvement is embedded into research and that lived experience advisors are supported effectively-both emotionally and financially. Sarah Knowles (University of York) has recently curated materials for researchers to facilitate effective co-creation and patient and public involvement in the digital world. 9 For all research to be considered ethical, the benefits must be high and the risk minimised. The research community must be very clear about who will benefit from the research, how it can be implemented to inform policy and practice, and in what time frame. Clearly, ethics committees across the globe have a vital role to play in weighing these issues and in the context of a growing plethora of online studies. Given social distancing and lockdowns, an effective digital response is crucial. Clinical mental health services globally are having to mobilise staff digitally and remotely to meet current need. The research community also needs to respond effectively to the COVID-19 pandemic, but we must ensure that what we are doing is ethical. AMS convene expert group to rapidly develop a mental health research response to COVID-19 Evaluating iatrogenic risk of youth suicide screening programs: a randomized controlled trial Does asking about suicide and related behaviours induce suicidal ideation? What is the evidence Uncovering key patterns in selfharm in adolescents: sequence analysis using the Card Sort Task for Selfharm (CaTS) The induction of mood via the WWW Is camouflaging autistic traits associated with suicidal thoughts and behaviours? Expanding the interpersonal psychological theory of suicide in an undergraduate student sample What do young adolescents think about taking part in longitudinal self-harm research? Findings from a school-based study Digital and remote codesign discussion We declare no competing interests.