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ReclutandoNCT07928687Registro de ClinicalTrials.gov

Feasibility Study of an Outdoor Strength Training Program for Older Adults

Exercise Training

LO ESENCIAL

De qué trata este estudio

El registro indica que este estudio recluta participantes. La disponibilidad puede variar por centro.

Tipo de estudio
De intervención
Fase
No aplica
Rango de edad
65 años - No especificado
Sexo admitido
Todos los sexos
Voluntarios sanos
Aceptados
Participantes
24 Estimado

Estos son puntos de partida, no una decisión de elegibilidad. El equipo debe revisar todos los requisitos.

Las explicaciones y la navegación están en español. Los textos proporcionados por el registro, incluidos títulos, resúmenes y criterios, se conservan en su idioma original. Puedes pedir orientación en español a WCR.

Acerca de la investigación

In order to promote healthy ageing and independent living, the World Health Organization recommends older adults to engage in resistance exercise at least twice weekly. However, only a minority of the older population complies with these guidelines, stressing the urgent need to develop comprehensive strategies to implement resistance exercise programs in the community. This PhD project will be performed in close collaboration with IPitup vzw, who developed outdoor activity benches, an accommodating smartphone app with exercise instructions and training courses as a low-cost modality for resistance exercise in the general population. The aim is to build upon these existing structures and develop an optimized, progressive resistance exercise program for community-dwelling older adults, which can be performed in small groups without the need for specialized training experts. The program's feasibility, defined in terms of safety, adherence, usability and acceptability, will be tested.

¿Quién podría participar?

La lista siguiente contiene el texto del patrocinador. Puede incluir condiciones, tratamientos previos, resultados de pruebas y otros requisitos. Aparecer en tu búsqueda no significa que califiques.

Inclusion Criteria:

  • Community-dwelling adults
  • At least 65 years old

Exclusion Criteria:

  • Participation in an interventional study with an investigational medicinal product (IMP) or device
  • Systematic engagement in resistance exercise during the past year
  • Self-reported, unstable cardiovascular disease, neuromuscular disease, acute infection or fever
  • Self-reported, surgery in the past year
  • Self-reported injuries that result in the inability to perform study-related tasks
  • Inability to understand the test and training procedures because of cognitive problems
Entiende la evaluación inicial

Tratamiento, grupos y participación

El registro puede describir tratamientos y duración sin incluir un calendario completo. Pide al equipo las visitas, procedimientos, riesgos, costos y alternativas. Mantén tu atención habitual salvo que tu médico te indique un cambio.

Asignación
No aplica
Enmascaramiento
Sin enmascaramiento
Peer-supported outdoor strength training

Participants take part in a 6-week outdoor strength training program using activity benches and a smartphone application. Training is performed in small groups of six community-dwelling older adults. Within each group, one participant acts as a peer coach and provides practical support and motivation.

Other: 6-week outdoor strength training program using activity benches and a smartphone application

6-week outdoor strength training program using activity benches and a smartphone application OTHER

2x/week, 35-45min sessions at the outdoor activity bench

Prepara tus preguntas

Qué evalúan los investigadores

Estas medidas indican qué se estudia. No prueban que un tratamiento funcione.

Medidas principales

Number of Participants Experiencing Adverse Events

Plazo: Throughout the 6-week intervention

Safety of the intervention, assessed as the number of participants experiencing one or more adverse events related to testing or training sessions during the intervention period.

Participant Adherence Rate

Plazo: Throughout the 10-week study period

Adherence to the intervention, assessed as the proportion of participants who complete the intervention and post-intervention assessments. And assessed as the percentage of scheduled training sessions attended by participants during the 6-week intervention.

System Usability Scale (SUS)

Plazo: Post-intervention at week 9

Usability of the intervention will be assessed using the System Usability Scale (SUS), a 10-item questionnaire yielding a total score ranging from 0 to 5. Five items are positively worded, for which higher response scores indicate greater usability, while five items are negatively worded and are reverse-scored, such that lower response scores indicate greater usability.

Net Promoter Score (NPS)

Plazo: Post-intervention at week 9

Acceptability of the intervention, assessed using the Net Promoter Score (NPS), based on participants' likelihood of recommending the programme to others. Scores range from 0 to 10, with higher scores indicating greater acceptability and willingness to recommend the intervention.

Participant Acceptability of the Intervention

Plazo: Post-intervention at week 9

Acceptability of the intervention, assessed through participant feedback regarding the peer-led delivery model and the appropriateness of training intensity and progression. Responses will be summarized descriptively.

Completion Rate of Data Collection Procedures

Plazo: Over the 10-week study period

Feasibility of data collection procedures, assessed as the proportion of planned laboratory-based assessments, questionnaire assessments, and IPitup app-based assessments successfully completed by participants. Higher percentages indicate greater feasibility of the data collection procedures.

Change in Lower Limb Muscle Strength and Power

Plazo: Baseline at week 1 and post-intervention at week 9

Preliminary effects of the intervention on muscle strength and power, assessed as the change in lower limb muscle strength and power from baseline to post-intervention. Muscle strength and power will be measured using the predefined study strength assessment protocol. Higher values indicate greater muscle strength and power.

Implementation Barriers and Facilitators Identified During Focus Groups

Plazo: Post-intervention at week 10

Implementation barriers and facilitators will be explored through semi-structured focus groups conducted following the intervention. Audio recordings will be transcribed verbatim and analysed using qualitative thematic analysis. Identified barriers and facilitators will be categorized into themes to inform optimization of a future randomized controlled trial.

El registro no indica resultados publicados.

Revisa las tablas completas y sus limitaciones en el registro oficial.

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Centros de investigación (1)

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1 centros

KU Leuven - Department of Movement SciencesLeuven, Vlaams-Brabant, BelgiumReclutando

Equipo y fechas

Patrocinador principal
Universitaire Ziekenhuizen KU Leuven
Inicio del estudio
18 ago 2026 Real
Finalización primaria
4 nov 2026 Estimado
Finalización del estudio
4 nov 2026 Estimado
Primera publicación
10 nov 2026 Real
Última actualización
10 nov 2026 Real

Contactos oficiales del estudio

Prof. Christophe DelecluseCONTACTchristophe.delecluse@kuleuven.be+32 16 32 90 76
Título oficial del estudio

Development and Implementation of Resistance Training Programs in Community-dwelling Older Adults Using Outdoor Activity Benches: a Feasibility and Pilot Study.

EL PRÓXIMO PASO, CON APOYO HUMANO

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Fuente: API v2 de ClinicalTrials.gov. Patrocinadores e investigadores envían la información. La NLM no aprueba la seguridad ni la ciencia de todos los estudios registrados. Aviso del registro.

Consultado: 12 nov 2026 · Última actualización del registro: 10 nov 2026