Comparison of Capsular Stretching and Passive Joint Mobilization in Idiopathic Adhesive Capsulitis

Sponsor
Riphah International University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05903768
Collaborator
(none)
38
1
2
7.6
5

Study Details

Study Description

Brief Summary

The aim of this research is to determine the effects of capsular stretching versus passive joint mobilization on Pain, range of motion and Quality of life in patients with Idiopathic Adhesive capsulitis.

Condition or Disease Intervention/Treatment Phase
  • Other: Mobilization
  • Other: Cyriax capsular stretching
N/A

Detailed Description

In reference study, patients with Adhesive capsulitis were given the option to examine the immediate effects of posterior capsule stretching and scapular mobilization. They came to the conclusion that extending the posterior capsule improved shoulder range of motion. Current study will assess all shoulder movements and also showing effect on Quality of life of patients with adhesive capsulitis.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
38 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Comparison of Capsular Stretching and Passive Joint Mobilization in Idiopathic Adhesive Capsulitis
Actual Study Start Date :
Nov 1, 2022
Anticipated Primary Completion Date :
Jun 15, 2023
Anticipated Study Completion Date :
Jun 20, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Cyriax capsular stretching

Patient will be subjected to Hot Pack prior to treatment. Detailed intervention will include Active range of motion exercises,Home plan exercises.Anterior, Posterior and inferior capsular stretching.

Other: Cyriax capsular stretching
Hot Pack for 5mins,Active range of motion exercises (10 reps x 3 sets),Home plan include: wand exercises, wall-walking exercises, pendulum exercises,towel stretch exercises, Cross Body Adduction (10reps x 2 sets, each)Cold pack for 5 mins. Anterior, Posterior and inferior capsular stretching would be performed. Each stretch should be held15-30 seconds and repeated 2 to 4 times.

Active Comparator: Mobilization

Patient will be subjected to Hot Pack prior to treatment. Detailed intervention will include Active range of motion exercises,Home plan exercises and Maitland's Mobilization:

Other: Mobilization
Hot Pack for 5mins,Active range of motion exercises (10 reps x 3 sets),Home plan include: wand exercises, wall-walking exercises, pendulum exercises,towel stretch exercises, Cross Body Adduction (10reps x 2 sets, each)Cold pack for 5 mins. Maitland's Mobilization: Inferior glide (10x3), posterior glide, (10 reps x 3 sets), anterior glide (10 reps x 3 sets)

Outcome Measures

Primary Outcome Measures

  1. Numeric Pain rating scale [4th week]

    The Numeric Pain rating scale is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain.

  2. Range of motion (shoulder flexion) [4th week]

    changes in shoulder flexion Range of motion from baseline to final session was measured

  3. Range of motion (shoulder extension) [4th week]

    changes in shoulder extension Range of motion from baseline to final session was measured

  4. Range of motion (shoulder abduction) [4th week]

    changes in shoulder abduction Range of motion from baseline to final session was measured

  5. Range of motion (shoulder external rotation) [4th week]

    changes in shoulder external rotation Range of motion from baseline to final session was measured

  6. Range of motion (internal rotation) [4th week]

    changes in shoulder internal rotation Range of motion from baseline to final session was measured

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Both genders

  • Age : 30-50 years

  • Pain and Restricted movements of shoulder.

  • Patient With Adhesive Capsulitis of Stage 2

Exclusion Criteria:
  • Patient with any Intrinsic Etiology such as Haemarthrosis, rheumatoid arthritis ,infection or gout

  • Patient with any severe trauma, Shoulder dislocation, subluxation or ligament injury of the shoulder

  • Fractures of the shoulder

  • Peripheral neurological involvement in the upper extremity.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Lady reading hospital Peshawar Khyber Pakhtunkhwa Pakistan 25000

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: Ramsha Tariq, MS-OMPT, Riphah International University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT05903768
Other Study ID Numbers:
  • Riphah IU Maria Safdar
First Posted:
Jun 15, 2023
Last Update Posted:
Jun 15, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Riphah International University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 15, 2023