Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
PHASE1/PHASE2
10 participants
INTERVENTIONAL
2026-01-06
2026-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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LIFT
Participants will receive a task-oriented resistance exercise program at home.
Task-oriented resistance exercise
The intervention program includes progressive resistance exercise and daily activity exercise, delivered over a six-week period with an ideal frequency of three sessions per week. Progressive resistance exercise will be provided through a combination of in-person and online sessions, while daily activity exercise will be delivered exclusively in person.
Interventions
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Task-oriented resistance exercise
The intervention program includes progressive resistance exercise and daily activity exercise, delivered over a six-week period with an ideal frequency of three sessions per week. Progressive resistance exercise will be provided through a combination of in-person and online sessions, while daily activity exercise will be delivered exclusively in person.
Eligibility Criteria
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Inclusion Criteria
* 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 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.
65 Years
90 Years
ALL
No
Sponsors
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University of Florida
OTHER
Responsible Party
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Principal Investigators
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Chiung-ju Liu Associate Professor, phD
Role: PRINCIPAL_INVESTIGATOR
University of Florida
Locations
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College of Public Health and Health Professions, University of Florida
Gainesville, Florida, United States
University of Florida
Gainesville, Florida, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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IRB202500835
Identifier Type: -
Identifier Source: org_study_id
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