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CareCoach Feasibility trial – part of the CareCoach programme: adapting and testing an intervention for carers of people with dementia

CareCoachWP3 - A feasibility trial to assess the design and deliverability of a multi-centre randomised controlled trial of the CareCoach package, part of the CareCoach programme: adapting and testing an intervention for carers of people with dementia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN12540555
Enrollment
42
Registered
2022-11-18
Start date
2023-06-19
Completion date
Unknown
Last updated
2026-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

The well-being of carers of people with dementia Other

Interventions

Participants will be randomised by a computer generated randomisation scheme on an individual participant level (1:1) stratified by site. They will be allocated to the CareCoach intervention group or

Sponsors

University of Exeter
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 years old or above 2. Spoken understanding of the English language (with the help of family translators if required) 3. Currently caring for a person with dementia (all subtypes, diagnosed within the last 5 years) 4. Has a first-degree relationship (spouse/partner, sibling, son or daughter) with a person with dementia; OR must have a close personal relationship with a person with dementia (e.g. in-law family member, close friend or neighbour) 5. Has capacity to give informed consent to participate; 6. Has access to the internet (via a home computer/laptop, iPad/tablet or mobile phone with internet capability)

Exclusion criteria

Exclusion criteria: 1. Potential participants with insufficient cognitive abilities to engage in the online programme 2. Overburdened, as determined by study staff. 3. If the person with dementia they care for currently resides in a care home

Design outcomes

Primary

MeasureTime frame
1. The recruitment rate will be recorded as the number of eligible participants who consented to participate in the study over the 6 month recruitment period. 2. The attrition rate will be recorded as the number of eligible participants who consented to participate in the study but had not completed the final 6 month follow-up measures.

Secondary

MeasureTime frame
Measured at baseline and 6 months: 1. The Caregiver Self-Efficacy Scale (CSES) 2. The Pearlin Mastery Scale (PMS) 3. The Perceived Stress Scale (PSS) 4. The Centre for Epidemiological Studies Depression scale (CES-D) 5. The Generalised Anxiety Disorder 7-item scale (GAD-7) 6. Scale measuring the Impact of DEmentia on CARers (SIDECAR-D) 7. Modified Client Service Receipt Inventory (CSRI) 8. EuroQol Health Related Quality of Life (EQ-5D-5L) 9. Patient Health Questionnaire (PHQ-9). 10. The Goal Attainment Scaling (GAS, intervention only) Carer proxy rating of the person with Dementia: 11. Neuropsychiatric Inventory (NPI-Q) 12. Proxy EuroQol Health Related Quality of Life (EQ-5D-5L) 13. A small subset of participants will be interviewed and qualitative data will assess whether the intervention is perceived as acceptable to participants.

Countries

England, United Kingdom, Wales

Contacts

Public ContactHelen Morse
carecoach@uea.ac.uk+44 1603 591120

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 15, 2026