Cross Fiber Fascial Manipulation and Stretching Techniques in Overhead Throwing Athletes

Sponsor
Riphah International University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05707026
Collaborator
(none)
40
1
2
12
3.3

Study Details

Study Description

Brief Summary

Athletic training and sports participation is to enhance athletic performance. Performance is however multifactorial i.e., depending upon several parameters including warm-up practice, training regimes and other interventions. Stretching techniques that focus on increasing posterior shoulder soft tissue flexibility are commonly incorporated into prevention and treatment programs for the overhead athletes. GIRD is usually managed by stretching and soft tissue release of posterior shoulder capsule. Fascial manipulation is a manual therapy technique used in the management of musculoskeletal disorders. This study aims to evaluate the comparative effects of cross fiber fascial manipulation with stretching techniques in overhead throwing athletes

Condition or Disease Intervention/Treatment Phase
  • Other: cross fiber fascial manipulation
  • Other: stretching techniques(sleeper stretch and cross body adduction stretch)
N/A

Detailed Description

This was a randomized clinical trial that was conducted at Pakistan sports board and Coaching center, Lahore. Non probability convenient sampling technique was used to collect the data as per inclusion criteria. 40 Participants of this study were randomly allocated into 2 Groups. 20 participants in each group. The group A received three sessions of fascial manipulation for two weeks. Group B received three sessions of sleeper stretch in a side lying position in 90o abduction, elbow at 90o flexion and then performed shoulder IR and cross-body adduction stretch in sitting position. Three sets of the each stretch positions were held for 30 seconds with a 1 minute break between sets. A universal goniometer was used to measure internal rotation, external rotation, horizontal abduction, ROWE score to assess function, pain, stability and motion, Numeric pain rating scale (NPRS) was used to assess pain. The data was analyzed via SPSS version 22.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Comparative Effects of Cross Fiber Fascial Manipulation and Stretching Techniques on Glenohumeral Internal Rotation Deficit in Overhead Throwing Athletes
Actual Study Start Date :
Feb 1, 2022
Anticipated Primary Completion Date :
Feb 1, 2023
Anticipated Study Completion Date :
Feb 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: cross fiber fascial manipulation

The group A received three sessions of fascial manipulation in two weeks. FM applied to densified Centre of Coordination (CC) points located on the myofascial sequences for 5 to 8 minutes at each CC point

Other: cross fiber fascial manipulation
The group A received three sessions of fascial manipulation in two weeks. FM applied for 5 to 8 minutes at each point.

Experimental: stretching techniques

Group B received three sessions of sleeper and cross body adduction stretches. Group B received three sessions of sleeper stretch in a side lying position in 90o abduction, elbow at 90o flexion and then performing shoulder IR and cross-body adduction stretch was done in sitting position. Three sets of the each stretch position were held for 30 seconds with a 1 minute break between sets

Other: stretching techniques(sleeper stretch and cross body adduction stretch)
Group B received three sessions of sleeper and cross body adduction stretches. Group B received three sessions of sleeper stretch in a side lying position in 90o abduction, elbow at 90o flexion and then performing shoulder IR and cross-body adduction stretch was done in sitting position. Three sets of the each stretch position were held for 30 seconds with a 1 minute break between sets.

Outcome Measures

Primary Outcome Measures

  1. Goniometer [2 weeks]

    A universal goniometer was used to assess internal rotation, external rotation and horizontal adduction

  2. numeric pain rating scale [2 weeks]

    NPRS for pain assessment in overhead athletes reporting pain with GIRD, it is a subjective measure in which individual rate their pain on an 11-point numerical scale. The scale is composed of 0 (no pain at all) to 10( worst pain

  3. ROWE score composite [2 weeks]

    ROWE score for shoulder functional assessment(50), stability(30), pain(10) and motion(10). Total score is 100 thus 90-100=excellent ,70-89=good , 40-69=fair , less than 40 points=poor

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Active male and female athletes were included.

  • Age group was (18-40) .

  • Overhead throwing athletes(tennis, volleyball, bowlers) were included in this study)

  • Screening tests were taken to identify subjects with GIRD. GIRD was defined as more than 20o decrease in IR at 90o abduction in the dominant side compared to non-dominant side .

  • Subjects who rated shoulder pain 5 or more in NPRS/symptomatic with GIRD were recruited

Exclusion Criteria :
  • Any deformity

  • Any radiculopathy

  • Shoulder traumatic injuries( dislocation, subluxation, fracture)

  • Systemic illness

  • Subacromial impingement signs

Contacts and Locations

Locations

Site City State Country Postal Code
1 Pakistan Sports Board Lahore Punjab Pakistan 5433

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: aqsa nawaz, MS SPORTS pt, Riphah International University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT05707026
Other Study ID Numbers:
  • REC/RCR&AHS/22/0408
First Posted:
Jan 31, 2023
Last Update Posted:
Jan 31, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jan 31, 2023