The Effects of Spinal Mobilization Added to an Exercise Program in Recreational Tennis Players With Mechanical Low Back Pain
The Effects of Spinal Mobilization Added to an Exercise Program on Pain and Physical Fitness in Recreational Tennis Players With Mechanical Low Back Pain
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Tipo de estudio
Inscripción (Actual)
Inscripción
Fase
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Istanbul, Turquía (Türkiye)
- Istinye University
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Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Adults aged 18-45 years.
- Body mass index (BMI) between 18 and 30 kg/m².
- Mechanical low back pain that decreases in the supine position and increases with activity or in various postures.
- Low back pain of more than one week duration with a baseline intensity greater than 4 on the Visual Analog Scale (VAS) and unrelated to any defined medical condition.
- Playing tennis on a recreational basis at least 2 days per week, totalling at least 2 hours per week.
- Able to communicate in Turkish or English in both written and spoken form.
Exclusion Criteria:
- Pain in the lower back, hip, or groin lasting longer than 6 months.
- Pain accompanied by a sensory deficit.
- Pain radiating to the hip or lower extremity.
- History of long-term steroid use.
- Regular medication use.
- History of injury or surgery resulting in residual deficits.
- Previous interventional treatment to the lumbar region.
- Pregnancy or suspected pregnancy.
Termination Criteria During Study:
- Onset of an acute illness requiring treatment (e.g., influenza, pneumonia).
- Use of analgesic or sedative medication.
- An increase in VAS pain score greater than 3 points during exercise or treatment.
- Failure to perform the home exercise programme on three consecutive days.
- Missed manual therapy session.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
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Comparador activo: Control Group (CG):Home Exercise Program Only
Structured home-based exercise program performed daily for 3 weeks (21 sessions).
The program included posterior pelvic tilt, double knee-to-chest erector spinae stretching, combined hamstring and lumbar extensor stretching (long-sit toe touch), piriformis stretching, and static hamstring stretching.
Adherence was supported by written instructions, visual materials, and weekly telephone follow-up.
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21 daily sessions over 3 weeks; 5 repetitions per exercise (30-second holds for stretches; 10-second hold for posterior pelvic tilt); supported by written instructions, visual materials, and weekly telephone follow-up.
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Experimental: Experimental Group (EG): Spinal Mobilization Plus Home Exercise Program
The identical home exercise program (21 sessions over 3 weeks) plus four sessions of supervised spinal mobilization administered by a physiotherapist - one at baseline and one per week for 3 weeks - using Maitland-graded techniques (Levels I-V; end-range not forced).
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21 daily sessions over 3 weeks; 5 repetitions per exercise (30-second holds for stretches; 10-second hold for posterior pelvic tilt); supported by written instructions, visual materials, and weekly telephone follow-up.
Four supervised sessions over 3 weeks (one at baseline and weekly thereafter).
Techniques included thoracic posteroanterior mobilization (T5-T12), rotational thoracic mobilization ("butterfly/screw"), sacroiliac mobilization, side-lying lumbar mobilization, and anteroposterior lumbar mobilization.
Each technique was applied as five sets of one-minute oscillations with 20-second rest intervals in the posteroanterior, mediolateral, and transverse planes.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Visual Analog Scale (VAS) for pain during physical activity (cm
Periodo de tiempo: Baseline to Week 3
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Self-reported pain intensity during physical activity recorded on a 10-cm horizontal Visual Analog Scale anchored from 0 ("no pain") to 10 ("worst imaginable pain").
Lower values indicate less pain.
Safety Issue: No.
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Baseline to Week 3
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Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Visual Analog Scale (VAS) for pain at rest (cm)
Periodo de tiempo: Baseline to Week 3
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Self-reported pain intensity at rest recorded on a 10-cm horizontal Visual Analog Scale anchored from 0 ("no pain") to 10 ("worst imaginable pain").
Lower values indicate less pain.
Safety Issue: No.
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Baseline to Week 3
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Visual Analog Scale (VAS) for night pain (cm)
Periodo de tiempo: Baseline to Week 3
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Self-reported pain intensity during sleep/night recorded on a 10-cm horizontal Visual Analog Scale anchored from 0 ("no pain") to 10 ("worst imaginable pain").
Lower values indicate less pain.
Safety Issue: No.
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Baseline to Week 3
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Y-Balance Test (cm)
Periodo de tiempo: Baseline to Week 3
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Dynamic balance and neuromuscular control assessed by the maximum reach distance for each lower extremity in three directions (anterior, posteromedial, posterolateral).
Three trials per leg per direction; the maximum reach distance for each direction is recorded.
Higher values indicate better dynamic postural control.
Safety Issue: No.
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Baseline to Week 3
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Vertical Jump Test (cm)
Periodo de tiempo: Baseline to Week 3
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Maximal vertical jump height assessed using the validated My Jump Lab smartphone application (iPhone 15 Pro Max mounted on a flexible tripod 20 cm above the ground).
Three trials are performed barefoot on a hard surface with hands fixed on the hips; minimum, maximum, and mean values are recorded.
Higher values indicate better lower-extremity power.
Safety Issue: No.
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Baseline to Week 3
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Sit-and-Reach Test (cm)
Periodo de tiempo: Baseline to Week 3
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Hamstring and lumbar flexibility assessed using a Baseline sit-and-reach box.
From a long-sit position with the feet flat against the box and the knees fully extended, the participant reaches forward with both hands three times; the maximum reach distance from the foot reference line is recorded (positive when reaching beyond the toes; negative when not reaching the toes).
Higher values indicate greater flexibility.
Safety Issue: No.
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Baseline to Week 3
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Isometric Back-Chest-Leg Strength (kg-force)
Periodo de tiempo: Baseline to Week 3
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Maximal isometric strength of the back, chest, and lower-extremity extensor chain measured with a calibrated Baseline back-chest-leg dynamometer (New York, USA).
Following one practice trial, three trials are performed with 30-second rest intervals; the highest value is used in analysis.
Higher values indicate greater isometric strength.
Safety Issue: No.
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Baseline to Week 3
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Colaboradores e Investigadores
Patrocinador
Patrocinador
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
- Tennis - Spinal Mob 25-49
Plan de datos de participantes individuales (IPD)
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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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