- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07934108
Impact of Community-based Boxing Exercises in Individuals With Chronic Stroke
Impact of Community-based Non-contact Boxing Exercise on Individuals With Chronic Stroke - a Pilot Study
The purpose of this study is to examine if non-contact boxing exercises improve balance, physical performance, quality of life and physical activity in adults with chronic stroke. It will also learn about the physical activity trend in adults with chronic stroke. The main research questions of the study are:
- Do community-based non-contact boxing exercises improve the balance in participants with chronic stroke?
- How is the exercise intensity of boxing exercises in individuals with chronic stroke? Researchers will test one group of participants without a comparison group.
Participants will need to complete the following tasks over 8 weeks:
- Participate in the boxing exercise program once per week for 8 weeks
- Attend two evaluation sessions: the initial and the final evaluation sessions.
- Keep a diary of their daily step counts
- Learn to assess their own physical fatigue and mental fatigue level during boxing exercise sessions.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Each participant will receive a pedometer at the end of the initial evaluation session of the study. The pedometer will be used to track their daily step count. After 8 weeks, each participant will receive a gift card with a nominal value at the final evaluation session.
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Suh-Jen Lin, PT, PhD
- Número de teléfono: 2146897718
- Correo electrónico: slin@twu.edu
Copia de seguridad de contactos de estudio
- Nombre: Jyutika Mehta, PhD
- Número de teléfono: 214-689-6508
- Correo electrónico: jmehta@twu.edu
Ubicaciones de estudio
-
-
Texas
-
Dallas, Texas, Estados Unidos, 75235
- Reclutamiento
- The Mike A. Myers Stoke Center of Texas Woman's University - Dallas
-
Contacto:
- Jyutika Mehta, PhD
- Número de teléfono: 214-689-6508
- Correo electrónico: jmehta@twu.edu
-
Contacto:
- Suh-Jen Lin, PhD
- Número de teléfono: 214-689-7718
- Correo electrónico: slin@twu.edu
-
Investigador principal:
- Suh-Jen Lin, PhD
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
(1) Adults (age 18-80 years): (2) With chronic stroke (over 9 months), (3) Walk independently with or without an assistive device for a household distance (4) Montreal Cognitive Assessment (MoCA) score 23 or higher, (5) Self-report doing fine in daily activities (6) have passed the fall risk screening by the instructor (a physical therapist) of exercise program at the TWU Stroke Center to participate in the community-based group exercises.
Exclusion Criteria:
- with a hospital admission in 3 months,
- impaired cognition (MoCA score 22 or less)
- Dyspnea at rest
- with fever or self-report palpitation
- cannot walk for a household distance with an assistive device
- Currently active participation in other community exercise programs., receiving training at a physical therapy clinic, or self-exercise regularly on their own
- Inability to participate in one hour of low- to moderate-intensity exercise, even with frequent short breaks
- did not pass the fall risk screening during physical therapy examination
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Non-contact boxing exercise
non-contact group boxing exercises will be delivered at a community setting. |
The non-contact boxing exercise in delivered as a group once per week at a community-based setting for 8 weeks |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
The ABC scale
Periodo de tiempo: 8 weeks
|
The ABC scale is to assess balance confidence while performing various tasks without losing balance or feeling a state of unsteadiness. Some activities in the test include walking around the house, using stairs, reaching for objects, standing, and getting in and out of a car. |
8 weeks
|
|
PHQ-9
Periodo de tiempo: 8 weeks
|
The PHQ-9 is a 9-item questionnaire used to screen for the severity of depression based on Diagnostic and Statistical Manual of Mental Disorders (DSM) criteria. Each item is scored 0-3, reflecting how often symptoms occurred over the past two weeks. |
8 weeks
|
|
The Berg Balance Scale
Periodo de tiempo: 8 weeks
|
The Berg Balance Scale is a 14-item assessment that assesses static and functional balance in adults in order to determine fall risk. It consists of standing, sitting, and sit-to-stand while unsupported. The test also includes maintaining balance while reaching and head turning. |
8 weeks
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
The 10-Meter Walk Test
Periodo de tiempo: 8 weeks
|
The 10-Meter Walk Test is a gait speed assessment that requires the participant to walk 6 meters. Participants are asked to walk as fast as possible while maintaining their balance. They will be given 2 trials and gait speed will be calculated by taking the average of the two trials. |
8 weeks
|
|
Modified Clinical Test of Sensory Interaction on Balance:
Periodo de tiempo: 8 weeks
|
Modified Clinical Test of Sensory Interaction on Balance: This computerized test assesses an individual's postural sway and risk of falls at different conditions (30 seconds each): eyes open/firm surface, eyes closed/firm, eyes open/foam surface. eyes closed/foam surface. There are rails on both side of the platform that the participant can hold onto when needed, and two researchers will guard the participant with a gait belt. |
8 weeks
|
|
Physical activity
Periodo de tiempo: 8 weeks
|
Participants will wear a pedometer to track their daily step count and record on the activity log (on paper) over 8 weeks. The research team will call them every week to collect their previous 7-day step count data. |
8 weeks
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Director de estudio: Holly Hansen-Thomas, PhD, Texas Woman's University- Denton
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- IRB-FY 2026-141
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
The study protocol and statistical plan will be shared.
Marco de tiempo para compartir IPD
The IPD will be shared after completing the study (8/31/2028) for 3 years.
Tipo de información de apoyo para compartir IPD
- PROTOCOLO DE ESTUDIO
- SAVIA
- CIF
- RSC
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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