A global clinical measure of fitness and frailty in elderly people.
Kenneth Rockwood, Xiaowei Song, Chris MacKnight...
https://pubmed.ncbi.nlm.nih.gov/16129869/Actively Recruiting
Led by Centre Hospitalier Universitaire Saint Pierre · Updated on 2026-03-20
100
Participants Needed
1
Research Sites
N/A
Total Duration
This research focuses on people living with HIV PLWH aged 65 to 74, studying the development and prevention of frailty syndrome. Frailty involves multiple health issues, cognitive decline, and reduced physical reserves, leading to higher risks of hospitalizations and mortality. The study aims to understand how frailty affects this specific age group and validate a screening tool called the Fried scale in PLWH. Participants will be systematically screened using the Fried scale by a nurse before their physician visit. Those who screen positive for frailty risk will be referred for a specialized geriatric consultation to confirm their condition and receive a preventive care plan. After treatment, participants will complete a satisfaction questionnaire and undergo a follow-up Fried scale assessment one year later. Throughout the study, researchers will measure the number of PLWH aged 65 to 74 who have frailty or pre-frailty conditions at the start and one year later. The study involves regular screenings, consultations, and questionnaires to monitor participants health and satisfaction with care. This observational study will run until July 2028, with no experimental treatments involved.
CONDITIONS
A Pilot Project for PLWH Aged 65-75: Preventing the Development of Frailty
A
Agnes LIBOIS, MD
C
Charlotte Martin, MD, PHD
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Centre Hospitalier Universitaire Saint Pierre
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo assessments to evaluate their frailty status using the Fried scale.
1 visit (in-person)
Duration - 1 year
Participants are monitored for changes in frailty status over one year after the initial assessment.
1 visit after 1 year (in-person)
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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Lead Sponsor