Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06407817

Comparative Effects Of Spencer and Reverse Distraction Technique In Patients With Adhesive Capsulitis

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Riphah International University · Academic / Other
Sex
All
Age
40 Years – 60 Years
Healthy volunteers
Not accepted

Summary

To compare the effects of spencer and reverse distraction technique in patients with adhesive capsulitis

Detailed description

Adhesive capsulitis, also known as frozen shoulder, is an inflammatory condition characterized by shoulder stiffness, pain, and significant loss of passive range of motion. Adhesive capsulitis has a prevalence of approximately 2% to 5% in the general population, with a mean onset of age of 55. A randomized clinical trial will be conducted at Ibne Sina Hospital, Multan . Non probability convenience sampling technique will be applied on 50 patients who will be allocated through computerized randomization into group A \& group B to collect data. Group A will be given spencer technique and group B will be given reverse distraction technique along with baselines. The study will be completed within the time duration of ten months. Primary Outcome measures of the research will be pain, range of motion, function, muscle strength, disability and quality of life will be measured pre and post intervention. The whole treatment protocols will be given for four weeks. Data will be analyzed using SPSS software version 25. After assessing normality of data by Shapiro-wilk test, it will be decided either parametric or non-parametric test will be used within a group or between two groups.

Conditions

Interventions

TypeNameDescription
PROCEDURESpencer techniqueNo of repetitions; 3 sets for 10 repetitions with 1 minute rest between sets No Of Sessions Per Week: 3 Per Weeks for 6 weeks (40 Min per Session)
PROCEDUREreverse distraction techniqueNo of repetitions; 10 ( Shoulder Abduction)10 ( Shoulder Flexion) 10 (Shoulder External Rotation) No Of Sessions Per Week: 3 Per Weeks for 6 weeks (40 Min Per Session)

Timeline

Start date
2024-02-01
Primary completion
2025-01-01
Completion
2025-01-01
First posted
2024-05-09
Last updated
2024-12-27

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT06407817. Inclusion in this directory is not an endorsement.