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NCT Number: NCT06763601

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

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

Recruiting

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Key information

Age range

40 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Thumbay Physical Therapy and Rehabilitation Hospital

Ajman, United Arab Emirates

Location status: Recruiting

Location contact

Arulsingh

CONTACT

Ayesha seemab

CONTACT

Dr ram prasad muthukrishna

CONTACT

Dr sharad Patil

CONTACT

Dr sharad patil

CONTACT

+971 06 703 1555

sharmilla bano

CONTACT

[email protected]

+971 06 703 1555

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

SSMP, Isometric exercise, eccentric exercise, heavy slow resistance , functional program

Procedure

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

MWM,Isometric exercise, eccentric exercise, heavy slow resistance , functional program

Procedure

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

Procedure

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

Primary outcomes

  1. Shoulder Pain And Disability Index

    Time frame: from enrollment to week 4,6,8

    shoulder pain and disability index is use to measure shoulder pain and disability where 0 is the best score and 130 is the worst

  2. Numeric Pain Rating Scale

    Time frame: from enrollment to 8 weeks

    numeric pain rating scale where 0 indicates no pain and 10 indicates worst pain

Secondary outcomes

  1. Range Of Motion

    Time frame: week 4,6,8

    range of motion of shoulder joint that includes flexion, extension abduction, adduction, internal and external rotation

  2. Patients' Global Impression of Change (PGIC) scale

    Time frame: at enrollment and on 8th week

    PGIC is a 7 point scale depicting a patient's rating of overall improvement. where 1 indicates very much improved and 7 indicates worst

Study contacts

Contact information is provided by the study sponsor or research team.

Ayesha seemab, BPT

CONTACT

[email protected]

+971502423798

Watson Watson Arulsingh, PhD

CONTACT

[email protected]

+971505708763

Sponsors and collaborators

Lead sponsor

Gulf Medical University

Other

Registry information

Official study title

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

Acronym: SSMP

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jan 8, 2025
Registry last updated
Jan 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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