Cross Body vs Sleeper Stretch on Pain, Range of Motion and Functional Performance in Cricket Bowlers.

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Description

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

Study Overview

Start Date
October 20, 2023
Completion Date
February 20, 2024
Enrollment
22
Date Posted
February 5, 2024
Accepts Healthy Volunteers?
Yes
Gender
All

Locations

Full Address
Pakistan sports board
Lahore, Punjab 53700, Pakistan

Eligibility

Minimum Age (years)
20
Maximum Age (years)
30
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

Study Contact Info

Study Contact Name
Sana Batool, MS DPT
Study Contact Email
Study Contact Phone

Contact Listings Owner Form

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Other Details

FDA Regulated Drug?
No
FDA Regulated Device?
No
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.
NCTid (if applicable)
NCT06240819