Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

Effects of Exercise Intervention on Aging-related Motor Decline (EIAMD)

5 de febrero de 2020 actualizado por: VA Office of Research and Development

Effects of Exercise Intervention on Aging-related Motor Decline (AGING)

The purpose of this research study is to test whether differing levels of physical fitness affects patterns of motor dexterity and brain activity that have been shown to differ due to aging. Testing will take place at the Atlanta VA Medical Center and at Emory University.

Participants will be healthy adults within the target age range of 60-85 for the study. The study will require multiple visits over 15 months. There will be about 64 people volunteering for this study.

Descripción general del estudio

Descripción detallada

The U.S. Census reports over 14 million U.S. Veterans (>63%) are beyond mid-life (>55 years). Declines in upper extremity motor performance respective of strength and dexterity are well documented within this age cohort). Recent cross-sectional research has discovered that aging related motor deficits may be influenced by a loss of interhemispheric inhibition (IHI) between primary motor cortices. However, this loss may not be an inevitable consequence of aging. Work from previous VA OAA Predoctoral and CDA-1 awards have shown that aerobic fitness may serve to mitigate losses in interhemispheric inhibition assessed by both functional magnetic resonance imaging (fMRI) and transcranial magnetic stimulation (TMS). That is, individuals who are aerobically fit show higher levels of IHI and improved dexterity and reaction times.

In light of new evidence from the investigators' lab's recent cross-sectional studies, physical activity over the long term (at least 2-5 years) may serve to alter levels of IHI and improve motor performance in the upper extremity. Aerobic exercise may provide a mechanism (reduced loss of interhemispheric inhibition) that could serve to improve motor function, but the neural mechanism responsible for such effects remains unclear. Previous investigations of interhemispheric communication and exercise have been limited by nature of inquiry, as cross-sectional research cannot measure changes over time in participants. As such, it is currently unknown how exercise may directly affect levels of interhemispheric communication and motor performance.

Behavioral interventions (motor strength and coordination) have been shown to be effective in improving upper extremity motor performance in older adults, however the duration of these gains appear to be short-lived. After as little as a few weeks of detraining, motor strength and coordination in the upper extremity rapidly begins to return to pre-intervention levels. Evidence from exercise interventions assessing gait and locomotion have shown that exercise programs over a longer term (>6 months) are associated with improved proprioception, fewer falls and better balance. However, the comparison of outcomes of upper extremity function in elderly adults respective of exercise duration remains largely unexplored. In addition to comparing the effects of short-term exercise (3 months) versus behavioral training (3 months) on upper extremity function, the current proposal will evaluate if a longer-term (6 months) exercise program can maintain or enhance upper extremity function and associated levels of interhemispheric inhibition.

The current study proposes the next logical step in my line of research and directly investigates the effects of exercise in an intervention with sedentary older Veterans (50-80 years), a group most likely to exhibit aging-related motor deficits. The investigators propose to enroll 40 Veterans into an upper extremity dexterity improvement program involving behavioral and exercise components. The behavioral intervention is a muscle coordination training previously shown to improve unimanual motor performance in older adults. The exercise intervention is a supervised group cycling regimen. The figure below shows the study design. Interhemispheric communication will be assessed with fMRI, and TMS.

Tipo de estudio

Intervencionista

Inscripción (Actual)

33

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Georgia
      • Decatur, Georgia, Estados Unidos, 30033
        • Atlanta VA Medical and Rehab Center, Decatur, GA

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

60 años a 85 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Living persons between 60 and 85 years of age

Exclusion Criteria:

  • unmanaged diabetes
  • participants completing vigorous exercise per week
  • participants whose profession requires vigorous physical labor
  • contraindication to magnetic resonance imaging

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Ciencia básica
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Stretching Exercise Intervention
A. Light stretching and balance exercises under supervised trainer. 3 times per week for 20-45 minutes. HR will be targeted to be under 50% of age-related maximum.
A. Light stretching and balance exercises under supervised trainer. 3 times per week for 20-45 minutes. HR will be targeted to be under 50% of age-related maximum.
Experimental: Aerobic Exercise Intervention
B. Interval aerobic cycling under supervised trainer. 3 times per week for 20-45 minutes. HR will be targeted between 50-85% of age-related maximum.
Supervised weekly exercise. 3 bouts of 45 minutes weekly on a cycle ergometer. HR will be kept at 75% of age-related maximum.
Experimental: Self Monitoring Intervention
C. 6 month self-monitored training phase during which time participants will exercise using a take home bike ergometer.
6 month self-monitored training phase during which time participants will exercise according to prescribed regimen (cycling)

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Estimate Cardiovascular Efficiency After Aerobic Exercise
Periodo de tiempo: Baseline, 12 weeks, 24 weeks
Estimate of Volume of oxygen consumption (VO2peak) using YMCA protocol for cardiovascular assessment.
Baseline, 12 weeks, 24 weeks
Estimate of Cardiovascular Efficiency After Balance Training
Periodo de tiempo: Baseline, 12 weeks, 24 weeks
Estimated VO2peak using YMCA cycle test completed over nine to twelve minutes.
Baseline, 12 weeks, 24 weeks
Silent Period Duration After Exercise Cycling Program
Periodo de tiempo: Baseline, 12 weeks, 24 weeks
Duration of ipsilateral silent period from Transcranial magnetic stimulation measured in milliseconds
Baseline, 12 weeks, 24 weeks
Silent Period Duration for Balance Group
Periodo de tiempo: Baseline, 12 weeks, 24 weeks
Ipsilateral silent period duration as assessed by TMS
Baseline, 12 weeks, 24 weeks
fMRI Interhemispheric Inhibition Improvement After Aerobic Exercise
Periodo de tiempo: Baseline to 24 Weeks with cross-over
Participants who exercise will evidence larger increases in interhemispheric inhibition as assessed by functional magnetic resonance measured by a z-normalized area under curve of right primary motor cortex. The area under the curve is an estimate of the fMRI hemodynamic response impulse response function. A higher number of AUC indicates less interhemispheric inhibition. In contrast, a lower number in this analysis indicates higher interhemispheric inhibition.
Baseline to 24 Weeks with cross-over
fMRI Interhemispheric Inhibition Improvement After Balance Training
Periodo de tiempo: Baseline, 12 weeks, 24 weeks
Area under the curve of fMRI measures of right motor cortex BOLD profile will remain similar to pre measurements. The BOLD profile is the z-normalized area under the curve value of the fMRI impulse response function. A higher number indicates less interhemispheric inhibition.
Baseline, 12 weeks, 24 weeks
Comparison of Cardiovascular Efficiency for Aerobic Exercise First Group After Home-based Intervention
Periodo de tiempo: 24 and 48 weeks
Comparison of home based aerobic exercise intervention to assessments made after completion of crossover intervention in Participants receiving aerobic condition first. VO2peak estimation completed using the YMCA protocol investigating overall volume of oxygen consumption as a function of heart rate during work loads. Estimated VO2 peak values are in ml/kg(min).
24 and 48 weeks
Comparison of Cardiovascular Efficiency for Balance Exercise First Group After Home-based Intervention
Periodo de tiempo: 24 and 48 weeks
VO2peak estimation completed using the YMCA protocol investigating overall volume of oxygen consumption as a function of heart rate during work loads.
24 and 48 weeks
Comparison of Silent Period Duration After Aerobic Exercise
Periodo de tiempo: Baseline, 12 weeks, 24 weeks
Comparison of silent period duration at 24 weeks compared to baseline
Baseline, 12 weeks, 24 weeks
Comparison of Silent Period Duration After Balance Exercise
Periodo de tiempo: 24 and 48 weeks
Comparison of Home based training effects on TMS measures of silent period duration as compared to facility based exercise programs.
24 and 48 weeks

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Target Heart Rate Zone for Balance First Participants
Periodo de tiempo: 24 and 48 weeks
Heart rate in aerobic target zone is measured in percentage of time in at least 50% of participants heart rate reserve.
24 and 48 weeks
Target Heart Rate Zone After Aerobic Exercise First
Periodo de tiempo: 24 and 48 weeks
Targeted Heart Rate Zone among participants compared among short term exercise groups
24 and 48 weeks
Heart Rate Workload After Home Based Intervention
Periodo de tiempo: 24 and 48 weeks

Measured heart rate after home based intervention

Technical implementation at the facility level prevented acquisition of these metrics until late in the project.

24 and 48 weeks

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Keith M. McGregor, PhD MS BA, Atlanta VA Medical and Rehab Center, Decatur, GA

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

14 de enero de 2013

Finalización primaria (Actual)

7 de julio de 2018

Finalización del estudio (Actual)

1 de agosto de 2019

Fechas de registro del estudio

Enviado por primera vez

5 de febrero de 2013

Primero enviado que cumplió con los criterios de control de calidad

5 de febrero de 2013

Publicado por primera vez (Estimar)

8 de febrero de 2013

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

20 de febrero de 2020

Última actualización enviada que cumplió con los criterios de control de calidad

5 de febrero de 2020

Última verificación

1 de febrero de 2020

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • E0956-W
  • 2012-060697 (Otro número de subvención/financiamiento: Veterans Affairs)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

producto fabricado y exportado desde los EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Ensayos clínicos sobre Stretching Exercise Intervention

3
Suscribir