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Overhead Throwing AthletesNCT05707026

Cross Fiber Fascial Manipulation and Stretching Techniques in Overhead Throwing Athletes

A study testing cross fiber fascial manipulation and stretching techniques(sleeper stretch and cross body adduction stretch) in people with Overhead Throwing Athletes and Tennis Players, Bowlers, Volleyball Players, run by Riphah International University at 1 site in Pakistan.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 40 years
What is being tested?
cross fiber fascial manipulation and stretching techniques(sleeper stretch and cross body adduction stretch)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 sitePakistan
Study dates
1 Feb 2022to 1 Feb 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • 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

Who cannot join

  • Any deformity
  • Any radiculopathy
  • Shoulder traumatic injuries( dislocation, subluxation, fracture)
  • Systemic illness
  • Subacromial impingement signs

Trial locations and contacts

1 site in 1 country.

Aqsa Nawaz, MS contact

03083907800

aqsanawaz809@gmail.com

Pakistan1 site, 1 recruiting
  • Pakistan Sports Board

    Lahore, Punjab Province, 5433

    Aqsa Nawaz, MS SPORTS PT, 03083907800, aqsanawaz809@gmail.com

    Recruiting

Other trials in Pakistan

About this study

Official title: Comparative Effects of Cross Fiber Fascial Manipulation and Stretching Techniques on Glenohumeral Internal Rotation Deficit in Overhead Throwing Athletes

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

Read the 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.

Being tested
cross fiber fascial manipulation, stretching techniques(sleeper stretch and cross body adduction stretch)

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • cross fiber fascial manipulationOther

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

  • stretching techniques(sleeper stretch and cross body adduction stretch)Other

    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.

Study groups in NCT05707026
Study groupRoleWhat they receive
cross fiber fascial manipulationExperimentalThe 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
Receives: Other: cross fiber fascial manipulation
stretching techniquesExperimentalGroup 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
Receives: Other: stretching techniques(sleeper stretch and cross body adduction stretch)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Goniometer

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

    Measured: 2 weeks

  2. numeric pain rating scale

    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

    Measured: 2 weeks

  3. ROWE score composite

    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

    Measured: 2 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted31 Jan 2023
  2. Study start1 Feb 2022
  3. Primary completion1 Feb 2023 (estimated)
  4. Study completion1 Feb 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05707026
Sponsor's protocol ID
REC/RCR&AHS/22/0408
Status last verified
Jan 2023
First submitted
22 Jan 2023
Last updated
31 Jan 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing cross fiber fascial manipulation and stretching techniques(sleeper stretch and cross body adduction stretch) in people with Overhead Throwing Athletes and Tennis Players, Bowlers, Volleyball Players, run by Riphah International University at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 31 Jan 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Aqsa Nawaz, MS (03083907800, aqsanawaz809@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Goniometer (time frame: 2 weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Jan 2023.

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