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Effect of Shoulder Symptom Modification Procedure (SSMP) in Managing Patients with Frozen Shoulder

Effect of Shoulder Symptom Modification Procedure (SSMP) in Managing Patients with Frozen Shoulder: a Pilot Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06763601
Acronym
SSMP
Enrollment
36
Registered
2025-01-08
Start date
2025-01-01
Completion date
2025-05-16
Last updated
2025-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frozen Shoulder

Keywords

SSMP, MWM, sham mobilization, frozen shoulder

Brief summary

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

Interventions

PROCEDURESSMP, 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

PROCEDUREMWM,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

Sham mobilization followed by isometrics, eccentric training and heavy resistance training and finally the functional program .

Sponsors

Gulf Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

each participant will be randomly allocated one group. there are three groups in total

Eligibility

Sex/Gender
ALL
Age
40 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* • 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

Exclusion criteria

* Having any history of shoulder dislocation * Humerus fractures or trauma * Diagnosed with any sort of cancer * History of cardiovascular disease

Design outcomes

Primary

MeasureTime frameDescription
Shoulder Pain And Disability Indexfrom enrollment to week 4,6,8shoulder pain and disability index is use to measure shoulder pain and disability where 0 is the best score and 130 is the worst
Numeric Pain Rating Scalefrom enrollment to 8 weeksnumeric pain rating scale where 0 indicates no pain and 10 indicates worst pain

Secondary

MeasureTime frameDescription
Range Of Motionweek 4,6,8range of motion of shoulder joint that includes flexion, extension abduction, adduction, internal and external rotation
Patients' Global Impression of Change (PGIC) scaleat enrollment and on 8th weekPGIC is a 7 point scale depicting a patient's rating of overall improvement. where 1 indicates very much improved and 7 indicates worst

Countries

United Arab Emirates

Contacts

Primary ContactAyesha seemab, BPT
2023mpt08@mygmu.ac.ae+971502423798
Backup ContactWatson Watson Arulsingh, PhD
dr.watson@gmu.ac.ae+971505708763

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026