Evaluating the FRAILAP Program Combining Exercise and Geriatric Assessment to Improve Frailty in Adults Aged 70 and Over
Led by Alberto Bermejo Franco · Updated on 2026-08-07
200
Participants Needed
1
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
Frailty is a complex syndrome common among older adults that increases the risk of falls, disability, and other health problems. This research evaluates the FRAILAP program, which combines a Comprehensive Geriatric Assessment with a 12-week multicomponent exercise intervention, including visual-spatial gait retraining using the Tapiz Fisior system. The goal is to see if this approach improves frailty status, physical performance, and functional independence compared to usual care in adults aged 70 and older.
The trial involves two groups one receiving the FRAILAP program with supervised and home-based exercise sessions once a week each, plus health education on healthy lifestyles and fall prevention the other group receives standard primary care without the structured exercise program. The intervention lasts 12 weeks and includes exercises focused on strength, balance, mobility, flexibility, and gait retraining.
Participants will be assessed at the start and one week after the intervention ends, measuring frailty using the FRAIL Scale and physical performance with the Short Physical Performance Battery. Additional outcomes include falls, pain, mood, functional independence, nutrition, handgrip strength, comorbidities, and healthcare use. The study aims to support healthy aging through a practical program suitable for primary care settings.
CONDITIONS
Brief Title
Multicomponent Exercise and Comprehensive Geriatric Assessment Program (FRAIL+AP) for Frail Older Adults in Primary Care
Research Team
Á
Ángel Moisés Reyes Abreu, Registered Nurse
A
Alberto Bermejo Franco, PhD (Physiotherapy)
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Ability and willingness to provide written informed consent
Medical clearance to participate in low-to-moderate intensity physical exercise
Presence of frailty or pre-frailty defined by at least two criteria including FRAIL Scale score ≥ 1, SPPB score < 10, gait speed < 0.8 m/s, Timed Up and Go test > 12 seconds
Functional independence sufficient to participate (Barthel Index > 80)
Registered at one of the participating primary care centers
You will not qualify if you...
Absolute contraindications to physical exercise such as recent acute myocardial infarction, unstable angina, severe uncontrolled cardiovascular disease, or severe uncorrected aortic stenosis
Severe cognitive impairment preventing understanding of study procedures or exercise instructions
Severe psychiatric disorders interfering with participation
Absence of a legally authorized representative when required
Severe uncontrolled behavioral disturbances
Any acute or chronic medical condition deemed unsafe by investigators
Failure to attend the initial mandatory health education workshop
Attendance at fewer than 6 of the 12 scheduled supervised exercise sessions
Development of an acute medical condition contraindicating physical activity
Participant withdrawal of informed consent
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Intervention
Duration - 12 weeks
Participants in the intervention group receive a 12-week program including a comprehensive geriatric assessment, health education, and supervised plus home-based multicomponent exercise sessions featuring strength, balance, mobility, flexibility, and visual-spatial gait retraining using the Tapiz Fisior system. The control group receives standard primary care without the structured exercise program.
Weekly supervised and home-based sessions
Assessment
Duration - Up to 1 week after intervention
Participants undergo evaluations at baseline and one week after completing the intervention to measure frailty status, physical performance, falls, pain, mood, functional independence, nutrition, handgrip strength, comorbidities, and healthcare use.
2 visits (baseline and post-intervention)
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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