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El ensayo clínico NCT06763601 (SSMP) para Hombro congelado está reclutando. Consulte la vista de tarjeta del Radar de Ensayos Clínicos y las herramientas de descubrimiento de IA para conocer todos los detalles. O haga cualquier pregunta aquí. | ||
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Effect of Shoulder Symptom Modification Procedure (SSMP) in Managing Patients with Frozen Shoulder 36
Los detalles del ensayo clínico están disponibles principalmente en inglés. ¡Sin embargo, IA Trial Radar puede ayudar! Simplemente haga clic en 'Explicar el estudio' para ver y discutir la información del estudio en el idioma que haya seleccionado.
El ensayo clínico NCT06763601 (SSMP) es un estudio intervencionista para Hombro congelado. Su estado actual es: reclutando. El estudio se inició el 1 de enero de 2025, con el objetivo de reclutar a 36 participantes. Dirigido por Gulf Medical University, se espera que finalice el 16 de mayo de 2025. Los datos se actualizaron por última vez en ClinicalTrials.gov el 8 de enero de 2025.
Resumen
the study is about intervention to patient with frozen shoulder to help patients improve function and shoulder disability , reduce pain and improve range of motion, the main aim of this study is to find out which treatment intervention SSMP , MWM and sham mobilization give effective results
Título oficial
Effect of Shoulder Symptom Modification Procedure (SSMP) in Managing Patients with Frozen Shoulder: a Pilot Study
Condiciones médicas
Hombro congeladoOtros ID del estudio
- SSMP
- IRB-COHS-STD-112-Dec-2024
- Internal review board (Otro identificador) (Gulf medical University)
Número del NCT
Inicio del estudio (real)
2025-01-01
Última actualización
2025-01-08
Fecha de finalización (estimada)
2025-05-16
Inscripción (prevista)
36
Tipo de estudio
Intervencionista
FASE
N/A
Estado general
Reclutando
Palabras clave
SSMP
MWM
sham mobilization
frozen shoulder
MWM
sham mobilization
frozen shoulder
Objetivo principal
Tratamiento
Método de asignación
Aleatorizado
Modelo de intervención
Paralelo
Enmascaramiento
Simple ciego
Brazos / Intervenciones
| Grupo de participantes | Intervención/Tratamiento |
|---|---|
ExperimentalSSMP SSMP, Isometric exercise, eccentric exercise, heavy slow resistance , functional program | SSMP, Isometric exercise, eccentric exercise, heavy slow resistance , functional program In this group the patients will be given symptom modification procedure in the first phase followed by isometric exercises in second phase, eccentrics and HSR in third phase and functional program in fourth phase |
ExperimentalMWM MWM procedure followed by Isometric exercise, eccentric exercise, heavy slow resistance , functional program | MWM,Isometric exercise, eccentric exercise, heavy slow resistance , functional program in this mobilization with movement in first phase will be given followed by isometrics, eccentrics and heavy slow resistance exercise and finally the functional program |
Comparador placebosham mobilization Sham mobilization will be given for placebo effect followed by Isometric exercise, eccentric exercise, heavy slow resistance , functional program | sham mobilization Sham mobilization followed by isometrics, eccentric training and heavy resistance training and finally the functional program . |
Resultado primario
Resultado secundario
| Medida de resultado | Descripción de la medida | Periodo de tiempo |
|---|---|---|
Shoulder Pain And Disability Index | shoulder pain and disability index is use to measure shoulder pain and disability where 0 is the best score and 130 is the worst | from enrollment to week 4,6,8 |
Numeric Pain Rating Scale | numeric pain rating scale where 0 indicates no pain and 10 indicates worst pain | from enrollment to 8 weeks |
| Medida de resultado | Descripción de la medida | Periodo de tiempo |
|---|---|---|
Range Of Motion | range of motion of shoulder joint that includes flexion, extension abduction, adduction, internal and external rotation | week 4,6,8 |
Patients' Global Impression of Change (PGIC) scale | PGIC is a 7 point scale depicting a patient's rating of overall improvement. where 1 indicates very much improved and 7 indicates worst | at enrollment and on 8th week |
Asistente de participación
Criterios de elegibilidad
Criterios de edad
Adulto, Adulto mayor
Edad mínima
40 Years
Criterios de sexo
Todos
• Diagnosis of adhesive capsulitis confirmed by a healthcare professional.
- Scores more than 2 in adhesive capsulitis scale
- Range of motion affected in capsular pattern
- Age between 40-65 years.
- Willingness to participate by signing informed consent
- Having any history of shoulder dislocation
- Humerus fractures or trauma
- Diagnosed with any sort of cancer
- History of cardiovascular disease
Contactos centrales del estudio
Contacto: Ayesha seemab, BPT, +971502423798, [email protected]
Contacto: Watson Watson Arulsingh, PhD, +971505708763, [email protected]
1 Centros del estudio en 1 países
Thumbay Physical Therapy and Rehabilitation Hospital, Ajman, United Arab Emirates
sharmilla bano, Contacto, +971 06 703 1555, [email protected]
Dr sharad patil, Contacto, +971 06 703 1555
Ayesha seemab, Contacto
Arulsingh, Contacto
Dr ram prasad muthukrishna, Contacto
Dr sharad Patil, Contacto
Reclutando