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

Not Applicable
Recruiting
Conditions
Pain
Physical Functional Performance
Range of Motion
Interventions
Other: Sleeper Stretch
Other: Cross Body Stretch
Registration Number
NCT06240819
Lead Sponsor
Riphah International University
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.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
22
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.
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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
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Sleeper StretchSleeper StretchSleeper stretch in a side lying position in 90o abduction, elbow at 90o flexion and then performing shoulder IR for three sets with three repetitions.
Cross Body StretchCross Body Stretchcross-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.
Primary Outcome Measures
NameTimeMethod
Shoulder Painpre and 6 weeks post interventional

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

Range of motionpre and 6 weeks post interventional

A universal goniometer will be used to measure ROM

Functional Performancepre and 6 weeks post interventional

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

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Pakistan sports board

🇵🇰

Lahore, Punjab, Pakistan

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