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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

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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 congelado
Otros 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
Objetivo principal
Tratamiento
Método de asignación
Aleatorizado
Modelo de intervención
Paralelo
Enmascaramiento
Simple ciego
Brazos / Intervenciones
Grupo de participantesIntervención/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
Medida de resultadoDescripción de la medidaPeriodo 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
Resultado secundario
Medida de resultadoDescripción de la medidaPeriodo 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
Gulf Medical University logoGulf Medical University
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