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The Yorkshire & Humber community ageing research study

The Yorkshire & Humber Community Ageing Research (CARE) observational cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN16588124
Enrollment
1000
Registered
2015-05-06
Start date
2014-12-30
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

Older people (>75 years) with and without frailty Signs and Symptoms Frailty

Interventions

There are no interventions in this observational study. Community dwelling older people (aged 75 years and over) will be eligible for the CARE study. We have developed and validated an electronic fra

Sponsors

Bradford Teaching Hospitals Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Current participant inclusion criteria as of 03/05/2018: 1. Aged 75 years or older 2. Live in community 3. Identified as fit and or with mild, moderate and severe frailty (for pilot phase and main study) Previous inclusion criteria: 1. Aged 75 years or older 2. Live in community 3. Identified as fit and or with mild, moderate and severe frailty (for pilot phase) 4. Mild, moderate and severe frailty (for main study) The first 200 participants will be older people (>75 years) with and without frailty. The next 800 participants will be older people (>75 years) with frailty.

Exclusion criteria

Exclusion criteria: 1. Care home residents and people living at home who are bedbound 2. People with terminal cancer, 3. Those in receipt of the Amber Care Bundle (estimated life expectancy of three months or less) 4. People in receipt of palliative care services will also be excluded. Note – if participants go into a care home/nursing home after they have undertaken their initial baseline assessment, they will not be excluded and can continue if they are still willing to do so.

Design outcomes

Primary

MeasureTime frame
The minimum dataset required for the CARE study has been established on the basis of expert consensus, with due consideration of the cmRCT design and the range of primary outcomes required for future trials. For primary outcomes, we have therefore included: 1. Basic activities of daily living (ADL) (Barthel index) 2. Instrumental ADL (Notting Extended Activities of Daily Living) 3. Frailty (measured using phenotype model & cumulative deficit model) 4. Health-related quality of life (EQ5D) 5. General health (SF36) 6. Pain (geriatric pain measure) 7. Depression (geriatric depression scale) 8. Loneliness (de Jong Gierveld loneliness scale) All assessments will be undertaken at baseline (timepoint 1), 6 months (time point 2), 12 months (timepoint 3), 24 months (timepoint 4), 48 months (timepoint 5).

Secondary

MeasureTime frame
1. Health and social care resource use 2. Care home admission 3. Mortality 4. Cognition (Montreal Cognitive Assessment) 5. Hand grip strength assessment 6. Gait speed 7. Timed Up and Go test 8. Falls (self-report) All assessments will be undertaken at baseline (timepoint 1), 6 months (time point 2), 12 months (timepoint 3), 24 months (timepoint 4), 48 months (timepoint 5).

Countries

England, United Kingdom

Contacts

Public ContactLesley Brown
Lesley.brown@bthft.nhs.uk+44 (0)1274 383906

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 21, 2026