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.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
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 estudo
Inscrição (Estimado)
Estágio
- Não aplicável
Contactos e Locais
Contato de estudo
- Nome: Suh-Jen Lin, PT, PhD
- Número de telefone: 2146897718
- E-mail: slin@twu.edu
Estude backup de contato
- Nome: Jyutika Mehta, PhD
- Número de telefone: 214-689-6508
- E-mail: jmehta@twu.edu
Locais de estudo
-
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Texas
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Dallas, Texas, Estados Unidos, 75235
- Recrutamento
- The Mike A. Myers Stoke Center of Texas Woman's University - Dallas
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Contato:
- Jyutika Mehta, PhD
- Número de telefone: 214-689-6508
- E-mail: jmehta@twu.edu
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Contato:
- Suh-Jen Lin, PhD
- Número de telefone: 214-689-7718
- E-mail: slin@twu.edu
-
Investigador principal:
- Suh-Jen Lin, PhD
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
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
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Prevenção
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
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 |
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
The ABC scale
Prazo: 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
Prazo: 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
Prazo: 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 resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
The 10-Meter Walk Test
Prazo: 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:
Prazo: 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
Prazo: 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
- Diretor de estudo: Holly Hansen-Thomas, PhD, Texas Woman's University- Denton
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Outros números de identificação do estudo
- IRB-FY 2026-141
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
The study protocol and statistical plan will be shared.
Prazo de Compartilhamento de IPD
The IPD will be shared after completing the study (8/31/2028) for 3 years.
Tipo de informação de suporte de compartilhamento de IPD
- PROTOCOLO DE ESTUDO
- SEIVA
- CIF
- CSR
Informações sobre medicamentos e dispositivos, documentos de estudo
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