Compassion Pilot Intervention Study to Enhanced Integrated Care for People With Severe Memory Problems
Dementia
About this trial
This is an interventional supportive care trial for Dementia focused on measuring Terminal care, Residential facilities, Integrated health care systems, Interdisciplinary health team, Palliative care
Eligibility Criteria
Inclusion Criteria:
- residents residing in one of the two participating care homes;
- memory problems indicating a diagnosis of dementia according to the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV);
- Functional Assessment Staging scale (FAST) grade 6a (difficulty putting on clothing) and above (unable to hold head up) (Reisberg, 1988);
- Comorbidities or unmanaged symptoms such as agitation, recurrent infections, pain and pressure ulcers.
Exclusion Criteria:
- Residents who indicate either verbally or non-verbally that they do not wish to participate.
- Residents who are moribund, in a coma, or those where there are clinical concerns that may preclude them being approached.
Sites / Locations
- University College, London
Arms of the Study
Arm 1
Experimental
Compassion Intervention
Coordinated by the ICL who co-ordinates key activities at each site to address the two core components of the Intervention. Component 1 activities include: (a) person-centred assessment of residents, focussing on their physical, psychological, emotional and social needs, (b) meetings of the core care team (General practitioner, care home nurse and/or manager and ICL) and (c) meetings of the wider multidisciplinary care teams (including care home staff, ICL, and external healthcare professionals such as geriatrician, palliative care, mental health etc). Activities to facilitate component 2 include: (d) staff training sessions, education and support for staff and family carers. Training sessions are run by the ICL and logistics of training is planned at core meetings.