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Exploring the feasibility of implementing the Cognitive Daisy (COG-D) assessment in care homes to support individualised care

The Cognitive Daisy (COG-D) in care homes to support person-centred care: A feasibility cluster randomised trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN15208844
Enrollment
101
Registered
2022-09-28
Start date
2022-04-01
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Organic, including symptomatic, mental disorders Mental and Behavioural Disorders

Interventions

RESEARCH PLAN AND METHODS Please note: The research team will recruit one PDRA for 20 months (0.8) and 2 RA's for 12 months (0.6% to complete intervention activities in the care homes: staff training

Sponsors

University of Lincoln
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Care homes: 1. Residential or nursing home 2. Provides care to people with dementia 3. Has a minimum of 20 beds to facilitate recruitment of a sufficient number of residents in each care home Residents: 1. Consent to take part (personal or via consultation) Additional inclusion criteria for residents taking part in the COG-D assessment: 1. Can communicate well enough in English to not require an interpreter 2. Vision/hearing (with correction) adequate to participate in COG-D assessment 3. Deemed well enough by staff/researcher to complete the assessment by a member of staff or the assessor Care home staff: 1. Permanent, contracted, agency or bank member of staff at the time of data collection 2. Provide consent 3. Have sufficient proficiency in English to contribute to the data collection required for the research

Exclusion criteria

Exclusion criteria: Care homes: 1) Have already used COG-D 2) Subject to Care Quality Commission enforcement notices Local Authority quality concerns Residents: 1. Receiving end-of-life care. Care home staff: 1. Acting as a consultee for any residents participating in the trial

Design outcomes

Primary

MeasureTime frame
Effect signals of the COG-D intervention for residents will be investigated with the following (proxy) measures: 1. Quality of Life (QUALID) 2. Agitation (CMAI) 3. Independence on activities in daily living (BADLS) 4. Health Cost/resource usage (ED-5D-5L and medical records). For care staff, signals of effects will be explored for: 1. Sense of Competence in dementia care (SCIDS) 2. Burnout (CBI) 3. Understanding of COG-D and cognition (COG-D Q) All measures will be collected at baseline, and at 6 and 9 months post-randomisation. Pathways to the impact of the COG-D in care homes will be investigated in a process evaluation, exploring context and mechanisms of impact in interviews/focus groups with residents, staff, and family/relatives. Interviews will take place after the last collection of candidate outcome measures.

Secondary

MeasureTime frame
There are no secondary outcome measures

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 9, 2026