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El ensayo clínico NCT07125378 (LIFT) para Limitación de movilidad, Deterioro cognitivo está reclutando. Consulte la vista de tarjeta del Radar de Ensayos Clínicos y las herramientas de descubrimiento de IA para conocer todos los detalles. O haga cualquier pregunta aquí.
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Vivir la independencia a través del entrenamiento funcional (LIFT)

Reclutando
Los detalles del ensayo clínico están disponibles principalmente en inglés. ¡Sin embargo, IA Trial Radar puede ayudar! Simplemente haga clic en 'Explicar el ensayo' para ver y discutir la información del ensayo en el idioma que haya seleccionado.
El ensayo clínico NCT07125378 (LIFT) está diseñado para estudiar el tratamiento de Limitación de movilidad, Deterioro cognitivo. Es un estudio intervencionista de Fase I Fase II. Su estado actual es: reclutando. El ensayo se inició el 31 de enero de 2026, con el objetivo de reclutar a 10 participantes. Dirigido por la Universidad de la Florida, se espera que finalice el 31 de julio de 2026. Los datos se actualizaron por última vez en ClinicalTrials.gov el 25 de noviembre de 2025.
Resumen
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.
Título oficial

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

Condiciones médicas
Limitación de movilidadDeterioro cognitivo
Otros ID del ensayo
  • LIFT
  • IRB202500835
Número del NCT
NCT07125378
Inicio del ensayo (real)
2026-01-31
Última actualización
2025-11-25
Fecha de finalización (estimada)
2026-07-31
Inscripción (prevista)
10
Tipo de estudio
Intervencionista
FASE
Fase I
Fase II
Estado general
Reclutando
Palabras clave
Home-based intervention
Exercise
Older adults
Activities of daily living
Mobility
Cognition
Objetivo principal
Tratamiento
Método de asignación
N/A
Modelo de intervención
Grupo único
Enmascaramiento
Ninguno (Etiqueta abierta)
Brazos / Intervenciones
Grupo de participantesIntervención/Tratamiento
ExperimentalLIFT
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.
Resultado primario
Medida de resultadoDescripción de la medidaPeriodo de tiempo
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.
Resultado secundario
Medida de resultadoDescripción de la medidaPeriodo de tiempo
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
Criterios de elegibilidad

Criterios de edad
Adulto mayor
Edad mínima
65 Years
Criterios de sexo
Todos
  • 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.
University of Florida logoUniversidad de la Florida298 ensayos clínicos activos para explorar
Contactos centrales del ensayo
Contacto: Chiung-ju Liu Associate Professor, PhD, 352-273-6496, [email protected]
2 Sitios del ensayo en 1 países

Florida

College of Public Health and Health Professions, University of Florida, Gainesville, Florida, 32610, United States
Chiung-ju Liu, PhD, Contacto, 352-273-6495, [email protected]
Reclutando
University of Florida, Gainesville, Florida, 32610, United States
Chiung-ju Liu Associate Professor, PhD, Contacto, 352-273-6496, [email protected]
Aún no recluta