NCT05540301

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2016

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 8, 2016

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 23, 2017

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 6, 2017

Completed
5.4 years until next milestone

First Submitted

Initial submission to the registry

September 11, 2022

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 14, 2022

Completed
Last Updated

September 14, 2022

Status Verified

September 1, 2022

Enrollment Period

11 months

First QC Date

September 11, 2022

Last Update Submit

September 11, 2022

Conditions

Keywords

Sleeper StretchCross-Body StretchRange of MotionShoulderTennis Players

Outcome Measures

Primary Outcomes (2)

  • Internal rotation range of motion

    Internal rotation range of motion (ROM) was measured using the universal goniometer before and after the completion of the intervention. The greater the ROM, the better the prognosis.

    4 weeks.

  • Upper limb functions

    The Disability of the Arm, Shoulder, and Hand (DASH) scale was used to assess the upper limb functions. The DASH consists mainly of a 30-item disability/symptom scale, scored 0 (no disability) to 100. The higher the score, the worse the prognosis.

    4 weeks.

Study Arms (2)

Modified Sleeper Stretch Group

EXPERIMENTAL

Modified sleeper stretch was performed for four weeks.

Other: Modified sleeper stretching

Modified Cross-Body Adduction Stretch Group

ACTIVE COMPARATOR

Modified cross-body adduction stretch was performed for four weeks.

Other: Modified cross-body adduction stretch

Interventions

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

Modified Sleeper Stretch Group

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

Modified Cross-Body Adduction Stretch Group

Eligibility Criteria

Age20 Years - 35 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Lawn Tennis Players
  • Male
  • more than 15 degree glenohumeral internal rotation deficiency

You may not qualify if:

  • systemic or metabolic disorders
  • a positive test for labral lesions or rotator cuff tears
  • a history of recent fracture
  • a history of orthopaedic surgery in the upper limbs or cervical region

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

King Saud University

Riyadh, 11433, Saudi Arabia

Location

Study Officials

  • Masood Khan, M.P.Th

    King Saud University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Two-group two-factor research design was used.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 11, 2022

First Posted

September 14, 2022

Study Start

March 8, 2016

Primary Completion

January 23, 2017

Study Completion

April 6, 2017

Last Updated

September 14, 2022

Record last verified: 2022-09

Data Sharing

IPD Sharing
Will not share

Locations