Skip to main content
Clinical Trials/NCT06240819
NCT06240819RecruitingNot 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 enrollmentStarted: October 20, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
22
Locations
1
Primary Endpoint
Range of motion

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Outcomes Assessor)

Masking Description

the assessor who will take the readings is blind

Eligibility Criteria

Ages
20 Years to 30 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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

Arms & Interventions

Sleeper Stretch

Other

Sleeper stretch in a side lying position in 90o abduction, elbow at 90o flexion and then performing shoulder IR for three sets with three repetitions.

Intervention: Sleeper Stretch (Other)

Cross Body Stretch

Other

cross-body stretch will be done in sitting position. Three sets of the each stretch position would be held for 30 seconds with a 1 minute break between sets.

Intervention: Cross Body Stretch (Other)

Outcomes

Primary Outcomes

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

Shoulder Pain

Time Frame: pre and 6 weeks post interventional

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

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials