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Università della FloridaLiving Independence Through Functional Training (LIFT)
I dettagli dello studio clinico sono disponibili principalmente in inglese. Tuttavia, Trial Radar IA può essere d'aiuto! Basta cliccare su 'Spiega lo studio' per visualizzare e discutere le informazioni sullo studio nella lingua selezionata.
La sperimentazione clinica NCT07125378 (LIFT) è uno studio interventistico di Fase I Fase II volto a esaminare il trattamento per Limitazione della mobilità, Compromissione cognitiva, attualmente in arruolamento. Avviato il 31 gennaio 2026, prevede di arruolare 10 partecipanti. Sotto la guida di l'Università della Florida, dovrebbe concludersi entro il 31 luglio 2026. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 25 novembre 2025.
Sommario breve
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.
Titolo ufficiale
Living Independence Through Functional Training (LIFT): Feasibility of Hybrid Task-Oriented Resistance Exercise Following Home Health Discharge
Condizioni
Limitazione della mobilitàCompromissione cognitivaAltri ID dello studio
- LIFT
- IRB202500835
Numero NCT
Data di inizio (effettiva)
2026-01-31
Ultimo aggiornamento pubblicato
2025-11-25
Data di completamento (stimata)
2026-07-31
Arruolamento (previsto)
10
Tipo di studio
Interventistico
FASE
Fase I
Fase II
Fase II
Stato
In arruolamento
Parole chiave
Home-based intervention
Exercise
Older adults
Activities of daily living
Mobility
Cognition
Exercise
Older adults
Activities of daily living
Mobility
Cognition
Scopo principale
Trattamento
Allocazione
N.D.
Modello di intervento
A gruppo singolo
Mascheramento
Nessuno (studio in aperto)
Bracci / Interventi
| Gruppo/Braccio di partecipanti | Intervento/Trattamento |
|---|---|
SperimentaleLIFT 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. |
Esito primario
Esito secondario
| Misure di esito | Descrizione della misura | Arco temporale |
|---|---|---|
Short Physical Performance Battery | The score ranges from 0 to 12, with a score of 12 indicating the best physical functioning of the lower extremity. | Baseline, 8 weeks, and 12 weeks. |
Montreal Cognitive Assessment | The score ranges from 0 to 30, with a score of 30 indicating the best global cognitive function. | Baseline, 8 weeks, and 12 weeks. |
| Misure di esito | Descrizione della misura | Arco temporale |
|---|---|---|
Timed Up and Go Test-Single Task. | Time in seconds to complete the test, with a longer time indicating poor functional mobility. | Baseline, 8 weeks, and 12 weeks. |
Timed Up and Go-Dual Task | Time in seconds to complete the task, a longer time indicating the interference of the dual task effect on mobility. | Baseline, 8 weeks, and 12 weeks. |
List Sorting Working Memory Test | 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. | Baseline, 8 weeks, and 12 weeks. |
Dimensional Change Card Sort Test | 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. | Baseline, 8 weeks, 12 weeks. |
Flanker Inhibitory Control and Attention Test | The 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. | Baseline, 8 weeks, and 12 weeks |
Pattern Comparison Processing Speed Test | The raw score ranges from 0-133, with a higher score indicating better processing speed. The raw score is converted to a Change Sensitive Score. | Baseline, 8 weeks, and 12 weeks |
Speeded Matching Test | The 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. | Baseline, 8 weeks, 12 weeks |
Oral Symbol Digit Test | The raw score ranges from 0 to 143, with a higher score indicating better processing speed. The raw score is converted to a Rasch score. | Baseline, 8 weeks, and 12 weeks |
Criteri di eleggibilità
Età idonea
Adulto anziano
Età minima
65 Years
Sessi idonei
Tutti
- between the ages of 65 and 90
- received home health rehabilitation services within the last month
- 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
- plan to receive additional skilled rehabilitation services after home health discharge
- 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 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.
Università della Florida295 studi clinici attivi da esplorareContatti principali dello studio
Contatto: Chiung-ju Liu Associate Professor, PhD, 352-273-6496, [email protected]
2 Centri dello studio in 1 paesi
Florida
College of Public Health and Health Professions, University of Florida, Gainesville, Florida, 32610, United States
Chiung-ju Liu, PhD, Contatto, 352-273-6495, [email protected]
In arruolamento
University of Florida, Gainesville, Florida, 32610, United States
Chiung-ju Liu Associate Professor, PhD, Contatto, 352-273-6496, [email protected]
Non ancora in arruolamento