Living Independently with Functional Training
Official title: Living Independence Through Functional Training (LIFT): Feasibility of Hybrid Task-Oriented Resistance Exercise Following Home Health Discharge
Run by University of Florida · NCT07125378 · Data updated 2026-11-12
This six-week hybrid home- and clinic-based task-oriented resistance exercise program tests whether recently discharged older adults with mobility limitations and mild cognitive impairment can improve daily function and mobility.
Quick facts
| Phase | Phase1; Phase2 |
|---|---|
| Study type | Interventional |
| Ages | 65 Years to 90 Years |
| Sex | All |
| Enrollment | 15 (estimated) |
| Sponsor | University of Florida Academic / other |
| Locations | 2 sites (Gainesville, Florida and 1 other locations) |
| Status | Recruiting |
| Started | January 6, 2026 |
| Main results expected | November 30, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | July 31, 2026 |
| Trial ID | NCT07125378 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Community-dwelling adults aged 65–90 recently discharged from home health care who use a mobility aid or have slowed/unsteady gait, show cognitive decline on Mini MoCA, have a nearby care partner, and live within the study area with wireless connectivity.
✕Probably not a fit
Patients who cannot stand or walk even with an aid, have severe vision/hearing or communication impairments, reside in or plan to move to assisted living/long-term care, or plan to receive skilled rehabilitation are unlikely to benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This Phase 1/2 interventional program delivers a six-week hybrid task-oriented resistance exercise regimen to older adults recently discharged from home health care. Participants perform task-specific strength exercises at home with remote support, occasional in-person sessions, and continuous activity monitoring via a wearable tracker. Eligibility targets community-dwelling adults aged 65–90 with mobility limitations and cognitive decline (Mini MoCA <12), who have a nearby care partner and live within the study area. The trial measures feasibility, safety, adherence, and changes in mobility and activities of daily living.
Why it matters
Potential benefit: If successful, participants could gain better mobility and greater independence in daily activities, potentially reducing future care needs.
How similar studies have gone: Prior home-based and task-oriented resistance programs have shown improvements in mobility and daily function in older adults, though evidence is more limited for people with concurrent cognitive impairment.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * between the ages of 65 and 90 years * community-dwelling * live within a 50-mile radius of the study site with wireless connectivity in the area * mobility limitations as indicated by self-reported of using a mobility aid or having unsteady gait or walking slower than before * cognitive decline as indicated by a score \< 12 on Mini MoCA Version 2.1 * a care partner or adult family member living in the home or nearby * willing to wear an activity tracker during the study period Exclusion Criteria: * plan to receive skilled rehabilitation services * plan to move away outside the study area in two months * reside in an assisted living or long-term care facility or plan to relocate to such a facility in the next three months * severe vision or hearing loss that impedes activity performance or communication * unable to stand or walk even with a mobility aid * unable to follow a one-step command or carry on a conversation over the phone * unable to commit to the six-week exercise program * contradictions to resistance exercise, such as the end-stage heart failure * a terminal disease or on hospice care * a neurological condition affecting motor skills * not able to provide consent.
Where it's running
-
College of Public Health and Health Professions, University of Florida
Gainesville, Florida, United States Recruiting -
University of Florida
Gainesville, Florida, United States Not yet recruiting
Study contacts
- Principal investigator: Chiung-ju Liu Associate Professor, phD — University of Florida
- Study coordinator: Chiung-ju Liu Associate Professor, PhD
- Email: c.liu1@phhp.ufl.edu
- Phone: 352-273-6496
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.