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Sleeper's and Adduction Stretch to Increase Shoulder ROM

NCT05540301 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2022-09-14

No results posted yet for this study

Summary

The study aimed to compare the efficacy of modified sleeper stretch and modified cross-body adduction stretch in improving shoulder internal rotation range of motion and upper limb function. Thirty male lawn tennis players aged between 20 to 35, with more than 150 glenohumeral internal rotation deficiency (GIRD) on the dominant shoulder (compared to the nondominant side) participate in the study and divided into two groups (A and B). Group A received a modified sleeper stretch and group B received a modified cross-body adduction stretch for four weeks, five times per week. The outcome measures were the internal rotation range of motion measured by a universal goniometer and upper limb functions measured by the Disability of the Arm, Shoulder, and Hand (DASH) scale.

Conditions

  • Stiffness of Shoulder, Not Elsewhere Classified

Interventions

OTHER

Modified sleeper stretching

Modified sleeper stretching was performed on shoulder joint to increase internal rotation range of motion.

OTHER

Modified cross-body adduction stretch

Modified cross-body adduction stretching was performed on shoulder joint to increase internal rotation range of motion.

Sponsors & Collaborators

  • King Saud University

    lead OTHER

Principal Investigators

  • Masood Khan, M.P.Th · King Saud University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
35 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-03-08
Primary Completion
2017-01-23
Completion
2017-04-06

Countries

  • Saudi Arabia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05540301 on ClinicalTrials.gov