Whole Body Exercise in Spinal Cord Injury: Effects on Psychosocial Function
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Tipo de estudio
Tipo de estudio
Inscripción (Actual)
Inscripción
Fase
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Massachusetts
-
Cambridge, Massachusetts, Estados Unidos, 02139
- Spaulding Rehabilitation Network
-
-
Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
Adults (>18 years of age)
- Be in good health (asymptomatic for acute treatable illness) and medically cleared to exercise
- Own an iPhone or Android smartphone with the capacity to download and run the research platform (able to log into to the relevant app store, install the app on their own phone, and run the app).
- Be able to understand, communicate with and be understood by research personnel or Interpreters
- Be interested in participating and provide informed consent
- Have a SCI with motor or sensory deficits and use a wheelchair as primary means of mobility
- Have an injury level only as high as C4 to allow sufficient arm function for rowing
Exclusion Criteria:
- Participants will not have previously completed FESRT
- Acute illness
- Musculoskeletal injuries that have not healed completely
- Had heart surgery or are status post-myocardial infarction (MI) in the last 4 to 6 months, -Unstable angina
- Uncontrolled hypertension (systolic blood pressure ≥160 mm Hg and/or diastolic blood pressure ≥100 mm Hg)
- uncontrolled dysrhythmias
- Recent history of congestive heart failure that has not been evaluated and effectively treated
- Severe stenotic or regurgitant valvular disease
- Hypertrophic cardiomyopathy
- Unhealed pressure ulcer Stage 2 or higher at relevant contact sites during exercise.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
|
Experimental: FES-row-training
Subjects will perform 4 months of FES-row-raining
|
Hybrid FES Row Training using voluntary upper body and electrically-stimulated lower body
|
|
Otro: Wait-list time control
Subjects will wait 4 months before performing being allowed to engage in 4 months of FES-row-training
|
Hybrid FES Row Training using voluntary upper body and electrically-stimulated lower body
|
|
Comparador activo: Arms-only-row-training
Subjects will perform 4 months of arms-only row training before being allowed to engage in 4 months of FES-row-training
|
Hybrid FES Row Training using voluntary upper body and electrically-stimulated lower body
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Depression
Periodo de tiempo: Each week during the 4 months
|
Difference between groups in depression symptom severity (Patient Health Questionnaire-9); Within-individual Correlation of exercise intensity with depression
|
Each week during the 4 months
|
|
Pain Severity
Periodo de tiempo: Each week during the 4 months
|
Difference between groups in pain severity, rated on a 0-10 scale ("0 being no pain and 10 being pain so severe you couldn't stand it"); Within-individual Correlation of exercise intensity with pain.
|
Each week during the 4 months
|
|
Pain Interference
Periodo de tiempo: Each week during the 4 months
|
Difference between groups in pain interference in daily life activities ("0.
Not at all 1.
A little bit 2. Moderately 3. Quite a bit 4. Extremely"); Within-individual Correlation of exercise intensity with pain.
|
Each week during the 4 months
|
|
Anxiety
Periodo de tiempo: Each week during the 4 months
|
Difference between groups in anxiety (Spinal Cord Injury Quality of Life Anxiety Short Form); Within-individual Correlation of exercise intensity with anxiety.
Minimum score is 9, Maximum score is 45.
Higher scores indicate higher anxiety.
|
Each week during the 4 months
|
|
Satisfaction with Social Participation
Periodo de tiempo: Each week during the 4 months
|
Difference between groups in satisfaction with social roles and activities (Spinal Cord Injury Quality of Life Satisfaction with Social Roles and Activities Short Form); Within-individual Correlation of exercise intensity with satisfaction with social participation.
The Minimum score is 20 and the maximum score is 50.
Higher values indicate greater satisfaction with social participation.
|
Each week during the 4 months
|
|
Ability to participate in social roles
Periodo de tiempo: Each week during the 4 months
|
Difference between groups in ability to participate in social roles and activities.
Spinal Cord Injury Quality of Life Ability to Participate in Social Roles and Activities Short Form.
Within-individual Correlation of exercise intensity with ability to participate in social roles.
The Minimum score is 20 and the maximum score is 50.
Higher values indicate greater satisfaction with social participation.
|
Each week during the 4 months
|
Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Health Complications
Periodo de tiempo: Each week during the 4 months
|
Difference between groups in frequency of secondary health complications; Within-individual Correlation of exercise intensity with secondary health complications.
|
Each week during the 4 months
|
|
Community Mobility
Periodo de tiempo: Each week during the 4 months
|
Difference between groups in community mobility (Distance traveled each week); Within-individual Correlation of exercise intensity with community mobility.
|
Each week during the 4 months
|
|
Social Connectivity: Frequency
Periodo de tiempo: Each week during the 4 months
|
Difference between groups in social connectivity (Frequency of phone calls and text messages); Within-individual Correlation of exercise intensity with frequency of social connectivity.
|
Each week during the 4 months
|
|
Social Connectivity: Reciprocity
Periodo de tiempo: Each week during the 4 months
|
Difference between groups in social connectivity (Reciprocity of phone calls and text messages); Within-individual Correlation of exercise intensity with reciprocity of social connectivity.
|
Each week during the 4 months
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Colaboradores
Colaboradores
Investigadores
Investigadores
- Investigador principal: J. Andrew Taylor, Spaulding Rehabilitation Hospital/Harvard Medical School
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Inicio del estudio
Finalización primaria (Actual)
Finalización primaria
Finalización del estudio (Actual)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
Otros números de identificación del estudio
- 2017D006049
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
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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