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Clinical Trials/NCT06240819
NCT06240819
Recruiting
Not Applicable

Comparison of Cross Body and Sleeper Stretch on Pain, Range of Motion and Functional Performance in Cricket Bowlers With Glenohumeral Internal Rotation Deficiency(GIRD).

Riphah International University1 site in 1 country22 target enrollmentOctober 20, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
Riphah International University
Enrollment
22
Locations
1
Primary Endpoint
Shoulder Pain
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The study is randomized and single-blinded. Ethical approval is taken from ethical committee of Riphah International University, Lahore. Participants who meet the inclusion criteria will be enrolled and allocated in group A & B through sealed envelope method by Non-probability Convenient random sampling technique. Subjects in Group A will receive sleeper stretch in a side lying position. Group B will receive cross-body stretch will be done in sitting position

Detailed Description

The objective of the study is to determine the comparison of sleeper stretch and cross body stretch on pain, range of motion and functional performance in cricket bowlers with GIRD. The study is randomized and single-blinded. Ethical approval is taken from ethical committee of Riphah International University, Lahore. Participants who meet the inclusion criteria will be enrolled and allocated in group A \& B through sealed envelope method by Non-probability Convenient random sampling technique. Subjects in Group A will receive sleeper stretch in a side lying position. Group B will receive cross-body stretch will be done in sitting position. A universal goniometer, Upper limb functional index (UEFI) scale and Numeric pain rating scale (NPRS) will be used at the baseline and after the completion of treatment at 6 weeks. The data will be analyzed by SPSS, version 25. Statistical significance is P=0.05.

Registry
clinicaltrials.gov
Start Date
October 20, 2023
End Date
February 20, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age 20 to 30years,
  • Both male and female,
  • \>10% IR deficit,
  • \>25% IR deficit related to contralateral limb,
  • Athletes one year of regular practice,
  • Lift off test for shoulder internal rotation positive.

Exclusion Criteria

  • Non players,
  • Any nerve lesions of upper limb,
  • Players with history of shoulder pain or fracture or dislocation in less than twelve months

Outcomes

Primary Outcomes

Shoulder Pain

Time Frame: pre and 6 weeks post interventional

Numeric pain rating scale (NPRS) will be used to assess pain.

Range of motion

Time Frame: pre and 6 weeks post interventional

A universal goniometer will be used to measure ROM

Functional Performance

Time Frame: pre and 6 weeks post interventional

upper extremity functional index (UEFI) scale to assess functional performance

Study Sites (1)

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