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Effects of Specific inferior capsular stretching and Mobilization with movement in Adhesive capsulitis

Effects of Specific Inferior Capsular stretching and Mobilization with movement in Adhesive Capsulitis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200921048785N1
Enrollment
32
Registered
2020-10-25
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-11-09

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

Conditions

Adhesive Capsulitis of Shoulder. Adhesive capsulitis of shoulder/Frozen shoulder/Periarthritis of shoulder

Interventions

Intervention 1: Intervention group: Group A receiving Mobilization with movement. Intervention 2: Intervention group: Group B receiving Specific inferior capsular stretching.

Sponsors

Riphah International University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: Both male and female patients will be included Patients with frozen shoulder aged 40-60 years will be recruited Shoulder pain at night that often disturb sleep Difficulty in reaching behind the back Reduced arm swing with walking Stiff and painful shoulder more than 1 month Minimum 50% of restriction in abduction & external rotation of shoulder joint

Exclusion criteria

Exclusion criteria: Recent trauma in and around shoulder joint History of shoulder subluxation, dislocation, or ligamentous injury Intrinsic glenohumeral pathology as GH arthritis Previous surgeries Subjects with diabetes Surgical release of capsule Subjects on steroids or NSAIDs

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Baseline, Before 1st treatment session and after 12th treatment session of total 6 weeks treatment plan (pre/post). Method of measurement: Numeric Pain Rating Scale.;Range of motion. Timepoint: Baseline, Before 1st treatment session and after 12th treatment session of total 6 weeks treatment plan (pre/post). Method of measurement: Goniometer.

Secondary

MeasureTime frame
Pain & Function. Timepoint: Baseline, Before 1st treatment session and after 12th treatment session of total 6 weeks of treatment plan (pre/post). Method of measurement: Shoulder Pain and Disability Index (SPADI).

Countries

Pakistan

Contacts

Public ContactDr. Rabiya Noor

Riphah International University

rabiya.noor@riphah.edu.pk+92 42 35126110

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026