- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01245283
Resistance Exercise and Knee Osteoarthritis Pain, Functional Impairment and Cartilage Turnover
Comparative Resistance Exercise Effect on Knee Osteoarthritis Pain, Functional Impairment and Cartilage Turnover
Descripción general del estudio
Estado
Condiciones
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Florida
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Gainesville, Florida, Estados Unidos, 32607
- UF&Shands Orthopaedics and Sports Medicine Institute
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Osteoarthritis (OA) of the knee for >6 months
- moderate to severe pain immediately following a 50-foot walk
- knee pain primarily due to tibiofemoral OA and not from patellofemoral OA
- bilateral standing anterior-posterior radiograph demonstrating grade 2 or 3 OA of the target knee
- willing and able to participate in regular exercise for four months
- free from musculoskeletal limitations that would preclude resistance exercise participation
- free of abnormal cardiovascular responses during the screening graded maximal walk test
Exclusion Criteria:
- unable to walk
- regular resistance exercise training (>3X week) within the past 6 months
- specific low back pain or acute back injury
- spinal stenosis that precludes walking one block due to neurogenic claudication
- any major injury to either knee within the prior 12 months
- any surgery to either knee within the last 12 months
- lumbar radiculopathy
- vascular claudication
- significant anterior knee pain due to diagnosed isolated patella-femoral syndrome or chondromalacia in either knee
- have had corticosteroid or viscosupplement injections within three months of study participation
- have added new over the counter or prescription pain medication within two months of study participation
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Comparador activo: Wait-list Non-exercise Control (CON)
Subjects will continue to participate in their normal activities and clinical care during the four month study period if assigned to this group.
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Subjects will continue to participate in their normal activities and clinical care during the four month study.
Telephone contact will be made weekly to encourage adherence to the knee management guidelines
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Comparador activo: Concentric Focused RX (CRX)
Training protocol for 1 set of each exercise will be completed - leg press, leg curl, leg extension, chest press, seated row, overhead press, triceps dip, biceps curl, and calf press.
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Two resistance exercise sessions per week; 1 set of 10-12 repetitions of each exercise will be completed - leg press, leg curl, leg extension, chest press, seated row, overhead press, triceps dip, biceps curl, and calf press.
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Comparador activo: Eccentric Focused RX (ERX)
The Human Dynamics Laboratory features prototype equipment that increases resistance loads during the eccentric phase of the contraction while "assistance" is provided by the machine during the concentric phase.
One set of each exercise - leg press, leg curl, leg extension, chest press, seated row, overhead press, triceps dip, biceps curl, and calf press.
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Two resistance exercise sessions per week; 1 set of 10-12 repetitions of each exercise will be completed - leg press, leg curl, leg extension, chest press, seated row, overhead press, triceps dip, biceps curl, and calf press.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC Score); Change From Baseline at 4 Months
Periodo de tiempo: Baseline, 4 Months
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The WOMAC is a standard, multidimensional, self-administered functional-health status instrument for patients with lower limb OA. Subjects will complete the self-assessment at the time intervals indicated to document any change in their perception of their functional health status. Scale for Total score: the higher score means the worst the function and pain Total WOMAC scores will have a range of 0 to 96 (best and worst scores possible). 0-20 Womac pain (0= best, 20=worst) 0-8 Womac stiffness (0= best, 8=worst) 0-68 Womac functional (0= best, 68=worst) 0-96 Womac Total (0= best, 96=worst) |
Baseline, 4 Months
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Six Minute Walk Test; Change From Baseline at 4 Months
Periodo de tiempo: Baseline, 4 Months
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Each participant will walk at a self-selected pace in the lab around a pre-measured loop for a period of six minutes.
Subjects will complete the walk test at the time intervals indicated to document any change.
6 minute walk test is a baseline and 4 month post intervention measurement.
It is used to measure distance covered while walking during 6 minutes.
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Baseline, 4 Months
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Chair Rise Time and Stair Climb Time; Change From Baseline at 4 Months
Periodo de tiempo: Baseline, 4 Months
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Functional abilities related to moving body weight will be captured using two standard tests, the chair rise time and stair climb time.
Subjects will complete the tests at the time intervals indicated to document any change in their functional abilities.
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Baseline, 4 Months
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Leg Press Test; Change From Baseline at 4 Months
Periodo de tiempo: Baseline, 4 Months
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Each participant will do a one repetition maximum.
Participants will perform a leg press.
The leg press is a weight training exercise in which the individual pushes a weight or resistance away from them using their legs.
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Baseline, 4 Months
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Leg Extensions Test; Change From Baseline at 4 Months
Periodo de tiempo: Baseline, 4 Months
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Each participant perform a one repetition maximum .
Participants will perform a leg extension which is a resistance weight training exercise that targets the quadriceps muscle in the legs.
The exercise is done using a machine called the Leg Extension Machine.
This resistence is measured in pounds.
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Baseline, 4 Months
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Leg Curl Test; Change From Baseline at 4 Months
Periodo de tiempo: Baseline, 4 Months
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Each participant will perform a one repetition maximum.
Participant will perform a leg curl which is an isolation exercise that targets the hamstring muscles.
The exercise involves flexing the lower leg against resistance towards the buttocks.
This resistence is measured in pounds.
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Baseline, 4 Months
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Chest Press; Change From Baseline at 4 Months
Periodo de tiempo: Baseline, 4 Months
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Each participant will perform a one repetition maximum.
Participants will perform a chest press which is an upper body strength training exercise that consists of pressing a weight upwards from a supine position.
This resistence is measured in pounds.
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Baseline, 4 Months
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Shoulder Press Test; Change From Baseline at 4 Months
Periodo de tiempo: Baseline, 4 Months
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Each participant will perform a one repetition maximum.
Participants will perform the shoulder press which is a weight training exercise, typically performed while standing, in which a weight is pressed straight upwards from the shoulders until the arms are locked out overhead.
This resistence is measured in pounds.
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Baseline, 4 Months
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Seated Row Test; Change From Baseline at 4 Months
Periodo de tiempo: Baseline, 4 Months
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Each participant will perform a one repetition maximum.
Participants will do a seated row test which is pulling on a cable to lift weight from a seated row position.
This resistence is measured in pounds.
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Baseline, 4 Months
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Kevin R Vincent, M.D. Ph.D., University of Florida Department of Orthopaedics and Rehabilitaion
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 614-2009
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