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Living Independence Through Functional Training

Living Independence Through Functional Training (LIFT): Feasibility of Hybrid Task-Oriented Resistance Exercise Following Home Health Discharge

Status
Recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07125378
Acronym
LIFT
Enrollment
15
Registered
2025-08-15
Start date
2026-01-06
Completion date
2026-12-31
Last updated
2026-07-31

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

Conditions

Cognitive Impairment, Mobility Limitation

Keywords

Home-based intervention, Exercise, Older adults, Activities of daily living, Mobility, Cognition

Brief summary

The purpose of the research is to evaluate the feasibility and benefits of a six-week hybrid task-oriented resistance exercise program for older adults who have been recently discharged from home health care.

Interventions

BEHAVIORALTask-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.

Sponsors

University of Florida
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

One group with repeated measures at baseline, post-intervention, and one-month follow-up.

Eligibility

Sex/Gender
ALL
Age
65 Years to 90 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Short Physical Performance BatteryBaseline, 8 weeks, and 12 weeks.The score ranges from 0 to 12, with a score of 12 indicating the best physical functioning of the lower extremity.
Montreal Cognitive AssessmentBaseline, 8 weeks, and 12 weeks.The score ranges from 0 to 30, with a score of 30 indicating the best global cognitive function.

Secondary

MeasureTime frameDescription
Timed Up and Go Test-Single Task.Baseline, 8 weeks, and 12 weeks.Time in seconds to complete the test, with a longer time indicating poor functional mobility.
Timed Up and Go-Dual TaskBaseline, 8 weeks, and 12 weeks.Time in seconds to complete the task, a longer time indicating the interference of the dual task effect on mobility.
List Sorting Working Memory TestBaseline, 8 weeks, and 12 weeks.The raw score ranges from 0 to 24, with a higher score indicating better working memory. The raw score is converted to a Change Sensitive Score.
Dimensional Change Card Sort TestBaseline, 8 weeks, 12 weeks.The raw score ranges from 0 to 30, with a higher score indicating better executive function. The raw score is converted to a Change Sensitive Score.
Flanker Inhibitory Control and Attention TestBaseline, 8 weeks, and 12 weeksThe raw score ranges from 0 to 30, with a higher score indicating better executive function and attention. The raw score is converted to a Change Sensitive Score.
Pattern Comparison Processing Speed TestBaseline, 8 weeks, and 12 weeksThe raw score ranges from 0-133, with a higher score indicating better processing speed. The raw score is converted to a Change Sensitive Score.
Speeded Matching TestBaseline, 8 weeks, 12 weeksThe score ranges from 0 to 130, with a higher score indicating better speed of processing. The raw score is converted to a Change Sensitive Score.
Oral Symbol Digit TestBaseline, 8 weeks, and 12 weeksThe raw score ranges from 0 to 143, with a higher score indicating better processing speed. The raw score is converted to a Rasch score.

Countries

United States

Contacts

CONTACTChiung-ju Liu Associate Professor, PhD
c.liu1@phhp.ufl.edu352-273-6496
PRINCIPAL_INVESTIGATORChiung-ju Liu Associate Professor, phD

University of Florida

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 1, 2026