Geller Institute of Aging and Memory, University of West London
London, W5 5SA, United Kingdom
Location status: Recruiting
Location contact
Juliet Gillam, PhD
CONTACT
Rosie Dunn, PhD
CONTACT
NCT Number: NCT06937541
Study Goal: Understand carers' needs when someone with dementia is in a mental health ward and develop strategies to support carers as partners in care.
Research Questions:
* What are mental health wards like in terms of staff, patients, and current carer support? * What do carers experience and need during admission, discharge, and beyond? * How do ward routines and staff practices affect carer involvement? * How can co-design turn research into practical strategies for carer support? * Can these strategies be implemented effectively?
Method: The investigators will survey mental health wards nationwide, interview carers from three UK wards, observe ward practices, and talk to staff. They will use this information to create and share practical strategies to improve carer support across the UK.
Interested in participating?
Request InfoAll sexes
Observational
London, W5 5SA, United Kingdom
Location status: Recruiting
Juliet Gillam, PhD
CONTACT
Rosie Dunn, PhD
CONTACT
Background and rationale
Mental health wards (MHW) are a significant site of care for people living with dementia (PLWD), providing care for the most unwell, vulnerable, and high-risk individuals who are detained under the Mental Health Act (1983) for their own safety and the safety of others.
The UK has around 100 MHWs (80 NHS, 20 private) for PLWD, but there's a lack of evidence on care quality and experiences. Stays average 100 days, with most PLWD moving to institutional care rather than returning home.
Admissions often follow severe psychiatric or behavioural issues, such as self-harm or assaults. This population is at high risk to themselves and others, with high acuity and comorbidity. Admissions are complex, involving frequent unscheduled transfers to general hospitals, which are associated with high rates of falls and hospital-acquired infections.
Carer involvement can significantly improve clinical and social outcomes for people in mental health wards by reducing length of stay, promoting earlier discharge, and lowering relapse and readmission rates. Carers provide essential support that staff may not, ensuring person-centred care, advocacy, decision-making support, treatment adherence, and promoting recovery. However, carers often feel marginalized and describe MHWs as a place of 'battle,' experiencing high levels of trauma and distress with unmet emotional, social, and financial needs. Reviews and inquires highlight a culture that views carers as problematic and resource-intensive, leading to their support needs being overlooked.
There is an absence of research examining carer perspectives of MHWs and no evidence-based interventions to support carers of PLWD who are admitted within MHWs. In response, this study responds to urgent calls from the Department of Health and Social Care and NHS England, for partnership working with carers and families utilising co-production to develop effective interventions and training programmes to support carers and the guidance required by services and wards to support implementation.
Research question: How can MHWs effectively work in partnership with and support family carers of PLWD?
Aim and Objectives
This study will provide detailed understandings of carers experiences and involvement when PLWD are detained within a MHW, and staff rationales and responses to carers, throughout an admission. It will deliver new knowledge and evidence-based strategies co-designed to ensure carers are appropriately supported and involved and to improve patient outcomes.
Objectives:
Design
This mixed methods study uses a convergent parallel mixed methods design integrating a national mapping survey, interviews, ethnography and experience-based co-design and feasibility testing. This approach supports the collection of detailed data from multiple and contextualized perspectives, with the goal to improve healthcare systems.
The study uses family systems theory and the Family Adjustment and Adaptation Response Model (FARR) to understand family responses to stress, such as dementia and mental health admissions. It also incorporates anthropology and sociology theories to explore family and kinship in care contexts and how healthcare professionals and MHWs recognize and respond to families. This combined approach aims to understand carers' and families' experiences and how to best support them during MHW admissions.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Survey
Inclusion criteria
Exclusion criteria
Longitudinal interviews with current carers
Inclusion criteria
Exclusion criteria
Interviews with discharged carers
Inclusion criteria
Exclusion criteria
Interviews with People Living With Dementia (PLWD)
Inclusion criteria
Exclusion criteria
Co-design study - PLWD and carers
Inclusion criteria
Exclusion criteria
Co-design study - staff
Inclusion criteria
Exclusion criteria
Feasibility study - PLWD and carers
Inclusion criteria
Exclusion criteria
Feasibility study - staff
Inclusion criteria
Exclusion criteria
Time frame: 6 months
National mapping survey to gather data on the number/type of wards, patient and staff demographics and existing care provision for people living with dementia who are detained under the Mental Health Act and receiving care on a mental health ward.
Time frame: 1 year
Ethnographic observation of staff and family carers on the ward. The focus of the observations is on the organisation of care. Observations will take place from the corridor(s) of wards, in communal areas, typically at nursing stations or ward observation points. Short, 'in-situ' conversational interviews (around 5-10 minutes) will take place on the ward with staff. These will be unstructured conversations to capture 'in-the-moment' experiences. Observations and 'in-situ' conversations will be documented using a touch screen tablet device.
Time frame: 1 year
Interviews with carers across 3 NHS sites in the UK, who currently have a friend/relative with dementia receiving care on a mental health ward (8 carers per ward = 24 carers in total). Carers will be interviewed at 3 timepoints over 12 months to understand their experiences over time. Total number of interviews = 72. The sample of carers will be identified by ward managers. A semi-structured interview schedule will be used following a narrative interview approach.
Time frame: 1 year
Interviews with 'discharged' carers across 3 NHS sites, i.e. carers whose friend/relative with dementia had previously received care on a mental health ward and have been discharged from the ward within the last 3 years. 8 carers per ward = 24 interviews in total. The sample of carers will be identified via screening of ward records completed by ward managers at each ward. A letter and Participant Information Sheet (PIS) will be sent by post to invite discharged carers to participate in an interview. A semi-structured interview schedule will be used to capture their views and experiences.
Time frame: 1 year
Interviews with ward staff, such as nurses, healthcare assistants, psychiatrists across 3 NHS sites. 5 ward staff per site will be interviewed = 15 interviews. Ward staff will be identified in collaboration with ward managers. A semi-structured interview schedule will be used to capture their views and experiences.
Time frame: 6 months
Focus groups with staff to address:
i) acceptability, to what extent these strategies reflect current practice, constraints, and the potential for new approaches; ii) implementation, to what extent they can be successfully delivered; iii) integration, to what extent they can be integrated into routine practice iv) relevance and acceptability of the outputs created for PLWD, carers and families.
Three online focus groups of 8-10 participants (n=30) will provide opportunity for discussion to explore the structural and organisational barriers within wards that may facilitate or impede effective implementation.
Time frame: 6 months
PLWD, carers and families will be invited to share their perspectives around acceptability of the co-designed resources in a way that suits them most. This is a person-centered, inclusive approach to gathering feedback, where different approaches are paramount to suit different needs.
People with lived experience could share their feedback by annotating printed or electronic versions of documents, having a brief conversation with the researcher online, over the phone or in person via the researcher attending their PPI meetings.
Contact information is provided by the study sponsor or research team.
University of West London
Other
Acronym: FIND ME
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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