Wright, Kim https://orcid.org/0000-0003-3865-9743
Dodd, Alyson
Warren, Fiona C
Medina-Lara, Antonieta
Taylor, Rod
Jones, Steven
Owens, Christabel
Javaid, Mahmood
Dunn, Barney
Harvey, Julie E
Newbold, Alexandra
Lynch, Tom
Funding for this research was provided by:
National Institute for Health Research (PB-PG-1215-20023)
Article History
Received: 6 March 2018
Accepted: 19 September 2018
First Online: 16 October 2018
Ethics approval and consent to participate
: Ethics approval has been granted by the UK National Research Ethics Service, South Yorkshire Research Ethics Committee. Informed consent will be obtained following a multi-stage process. Participants will first give permission for the research team to contact them to discuss the study and for an initial screening call (for participants not referred by a mental health team). Following this, informed consent will be taken in person by a study researcher prior to the baseline eligibility and assessment interview. Potential participants will receive full information about the study in advance of the interview, and at the point of consent there will be further opportunity to discuss the study and for the participant to raise any questions. Researchers will be fully trained in taking informed consent, including assessment of capacity to consent where appropriate. Consent will be taken only from individuals with capacity to make an informed decision on their participation.
: Not applicable.
: The authors declare that they have no competing interests.
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