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Comprehensive Geriatric Assessment in Primary Care: A Randomised Feasibility Trial

'Comprehensive Geriatric Assessment' for Older Adults With Frailty Within Primary Care Setting: A Randomised Feasibility Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03394534
Enrollment
72
Registered
2018-01-09
Start date
2019-01-15
Completion date
2021-09-30
Last updated
2022-05-18

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

Conditions

Frailty

Keywords

Comprehensive Geriatric Assessment, Frailty, electronic Frailty Index, eFI, Care and Support plan, Primary Care

Brief summary

The study aims to explore feasibility of implementing a tailored CGA to older adults with frailty and evaluate staff and patients perception of the intervention. In line with this, the objectives of the study are: 1. To assess applicability of finding older adults with frailty using eFI and delivering subsequent CGA and care planning at patients' home 2. To investigate staff and older adults' perception of CGA programme 3. To assess the health care resource usage and cost of the CGA programme 4. To measure key health related outcome domains including function, quality of life, loneliness, pain, falls and mobility.

Interventions

OTHERCGA group

CGA Plus Individualised Care and Support Plan delivered by Advanced Clinical Practitioner (ACP)

Sponsors

Derbyshire Clinical Commissioning Groups
CollaboratorUNKNOWN
University of Derby
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to 95 Years
Healthy volunteers
No

Inclusion criteria

* Age 65 to 95 years * eFI score \> 0.12

Exclusion criteria

* Do not meet criteria for frailty based on Gait speed, timed up and go test and PRISMA questionnaire

Design outcomes

Primary

MeasureTime frameDescription
Hospitalisation and Nursing Home Admissionsat 6 months post interventionNumber of hospital and/or care home admissions during the 6 months period and reported in terms of admitted v. not admitted

Secondary

MeasureTime frameDescription
Lonelinessat baseline and 6 months post interventionImprove overall, emotional, and social loneliness calculated using the De Jong Gierveld Loneliness Scale total score. The scale is used to assess subjective perception of social participation or isolation in elderly adults.
Health related Quality of Lifeat baseline and 6 months post interventionChange in health related quality of life calculated using the 36-Item Short Form Survey (SF-36). The Sf-36 is patient reported outcome measure with a set of generic quality of life measures including vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning, mental health subscales.
Number of 999 calls and A+E attendance during the 6 months periodat 6 months post intervention
Functional Statusat baseline and 6 months post interventionImprove Patient functional ability measured using Functional Independence Measure (FIM) questionnaire total score
Length of time stayed in hospital or care home during the 6 months periodat 6 months post intervention
Therapist and staff time spent on CGA during the 6 months periodat 6 months post intervention
Number of GP/GP out of office attendance (including calls to GP) during the 6 months periodat 6 months post intervention
Length of time spent on A+E during the 6 months periodat 6 months post intervention

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026