Comparing two techniques for treating frozen shoulder
Comparative Effects Of Spencer and Reverse Distraction Technique In Patients With Adhesive Capsulitis
NA · Riphah International University · NCT06407817
This study is testing two different treatment methods for frozen shoulder to see which one helps people feel better and move their arms more easily.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 40 Years to 60 Years |
| Sex | All |
| Sponsor | Riphah International University (other) |
| Locations | 1 site (Lahore, Punjab Province) |
| Trial ID | NCT06407817 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to compare the effectiveness of the Spencer technique and the reverse distraction technique in patients suffering from adhesive capsulitis, commonly known as frozen shoulder. The study will involve 50 participants aged 40 to 60, who will be randomly assigned to one of the two treatment groups. Over a period of four weeks, the participants' pain levels, range of motion, muscle strength, and overall quality of life will be assessed before and after the interventions. Data analysis will be conducted using SPSS software to determine the outcomes of each technique.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 40 to 60 with stage 2 or 3 adhesive capsulitis and specific limitations in shoulder range of motion.
Not a fit: Patients with a history of shoulder surgery, fractures, neurological disorders, systemic arthritic conditions, or cervical spine disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide patients with more effective treatment options for managing adhesive capsulitis.
How similar studies have performed: While there is limited information on the specific techniques being compared, similar studies on adhesive capsulitis treatments have shown varying degrees of success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age group 40-60 years * Male and female * Positive Capsular pattern (ER more limited than Abd which is more limited than IR) * Limitation in shoulder ROM ; Flexion \<180 , Abduction \<180 , External Rotation \<50 * Patients of stage 2 and 3 of adhesive capsulitis Exclusion Criteria: * History of surgery of the affected shoulder * Fractures in around the shoulder * Neurological disorders leading to altered muscle activity * Systemic arthritic conditions (RA, Osteoporosis) * Disorders of the cervical spine
Where this trial is running
Lahore, Punjab Province
- Johar Pain Relief Center — Lahore, Punjab Province, Pakistan (RECRUITING)
Study contacts
- Principal investigator: Rabiya Noor, PHD — Riphah International University
- Study coordinator: Minal Mushtaq, MS-DPT
- Email: minalmustafakhan@gmail.com
- Phone: 03314662231
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Adhesive Capsulitis