- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT05130372
Comparison of The Acute Effects of Different Stretching Methods on Ankle Joint Range In Healty Older Adults
Comparison of The Acute Effects of Different Stretching Techniques on Ankle Joint Range of Motion In Healthy Older Adults: A Randomised Controlled Trial
Introduction: To compare the acute effects of different stretching methods on ankle joint range of motion (ROM) in older adults.
Methods: A total of 78 subjects aged 65 years and older were randomly divided into three groups. After the 5-minute walk, the randomly assigned method was applied. Static Stretching Group; static stretching in 3x30sec, PNF Stretching Group; PNF contract-relax in 3x30sec and Roller Massage Group; roller massage in 3x30sec was performed. Immediately after the application, 10 minutes and 20 minutes after application, the range of motion of the ankle joint was measured in the weight-bearing lunge position.
Descripción general del estudio
Estado
Condiciones
Descripción detallada
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Urla
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İzmir, Urla, Pavo
- Izmir Provincial Health Directorate State Hospital
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İzmir, Urla, Pavo
- Izmir Provincial Health Directorate Urla State Hospital
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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:
- Healthy and voluntary older adults aged 65 and over
- Who were able to walk without using an assistive device,
- Independent in their daily life activities
- Who scored 23 and above according to the mini-mental state test.
Exclusion Criteria:
- Presence of a neurological, orthopedic or cardiovascular disease affecting the lower extremity,
- Pain or limitation of movement in the ankle joint,
- Skin diseases,
- History of falling in the last 1 year,
- Any problem that may prevent lying prone
- participation in a regular exercise program.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Doble
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Comparador activo: Static Stretching Group
The static stretching method was actively applied while standing.The person was positioned facing the wall, supporting the wall with both hands, with the dominant foot behind.
The point where a feeling of tension in the plantar flexor muscles was created and held in this position for 30 seconds.
Afterward, a 15-second rest break was given.
After completing 3 repetitions (3x30sec) in total, measurements were started.
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Static stretching has been the most common stretching method applied to the ankle in healthy older adults, and different protocols have proven to increase ankle range of motion.
In this study, the static stretching method was actively applied while standing.
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Comparador activo: PNF Stretching Method Group
The person was positioned supine, and the ankle joint was dorsiflexed by the physiotherapist to the point where the tension was felt.
Then, while the person was trying to push the foot towards the plantarflexion direction for 10 seconds, the movement was prevented by the physiotherapist and isometric contraction was achieved at 20% of the maximum voluntary contraction.
After 10 seconds, the person was asked to relax slowly and passive stretching was applied to the plantar flexors for 20 seconds.
The contract-relax technique was applied for 30 seconds and completed with 3 repetitions (3x30sec) with 15-second rest intervals.
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The contract-relax technique was used in the PNF stretching method.
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Comparador activo: Myofascial Relaxation Method Group
A comfortable position was achieved by placing a rolled towel on the front of the ankle.
The roller was massaged along with the plantar flexors for 30 seconds.
The movement of the cylinder from bottom to top and from top to bottom was done for a second.
Three repetitions were completed (3x30sec) with a 15-second rest break.
For the pressure of the roller to be stable during the application, the numbered pain scale was shown to the participants, and attention was paid to ensure that the perceived severity was 7/10 according to the numbered pain scale.
Participants with dry skin in the application area were asked to moisturize with cream beforehand to avoid complications.
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A theraband roller massager (Theraband®, The Hygenic Corporation, Akron, OH) was used for the myofascial relaxation method.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Range of motion
Periodo de tiempo: Baseline
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The ankle ROM measurement made in the standing load-bearing position and the measurement made in the weight-bearing position.
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Baseline
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Range of motion
Periodo de tiempo: Immediately after application
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The ankle ROM measurement made in the standing load-bearing position and the measurement made in the weight-bearing position.
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Immediately after application
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Range of motion
Periodo de tiempo: 10 minutes after application
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The ankle ROM measurement made in the standing load-bearing position and the measurement made in the weight-bearing position.
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10 minutes after application
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Range of motion
Periodo de tiempo: 20 minutes after application
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The ankle ROM measurement made in the standing load-bearing position and the measurement made in the weight-bearing position.
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20 minutes after application
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Director de estudio: Ceren Devrim Şahin, MSc, Dokuz Eylül University
- Silla de estudio: Nursen İlçin, Assoc. prof., Dokuz Eylül University
- Investigador principal: Kutay Kaşlı, MSc, Çankırı Karatekin University
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
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 (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
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 2017/17-39
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan 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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