- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06304402
Comparing Shoulder Stretching and Percussive Massage on Shoulder Rotation and Attack Speed in Female Volleyball Players
July 12, 2024 updated by: Gonca Şahiner Pıçak, Dokuz Eylul University
Comparison of the Effects of Shoulder Stretching Exercise and Percussive Massage Treatment on Shoulder Rotation Movements and Attack Speed in Female Volleyball Players
This study aims to investigate the acute effects of PNF modified sleeper stretches and percussive massage treatment on shoulder rotation movements and attack speed in female volleyball players and compare these applications.
Study Overview
Status
Completed
Conditions
Detailed Description
56 female volleyball players will randomized into 2 groups of 28 people each.
In the evaluations conducted on the participants, rotational normal joint movements of the athletes will be measured using a digital inclinometer.
The spike velocities of the athletes will be determined using a sports radar (Sports Radar 3300, Sports Electronics Inc, Washington, D.C. USA.).
Participants will be randomly divided into two different groups consisting of 28 individuals each.
The Proprioceptive Neuromuscular Facilitation Stretching Group (PNFG) participants will undergo one session of PNF posterior shoulder stretching exercise in the modified sleeper position.
The Percussive Massage Treatment Group (PMTG) participants will receive a 5-minute massage on the posterior deltoid area.
Evaluations will be repeated three times before the applications, immediately after, and 30 minutes post-application and the effects of different applications will be compared through analysis.
Study Type
Interventional
Enrollment (Actual)
56
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Balçova
-
İzmir, Balçova, Turkey, 35340
- Dokuz Eylul University, School of Physical Therapy and Rehabilitation
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being a volleyball player
- Age between 14 and 40 years
Exclusion Criteria:
- Presence of shoulder pain
- History of fracture and surgery in the shoulder girdle
- Presence of systemic musculoskeletal disease
- Presence of glenohumeral instability (Positive apprehension, relocation, or subluxation test)
- Pain in the cervical region with upper extremity movements
- Experiencing shoulder problems requiring medical treatment within the last year
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Proprioceptive Neuromuscular Facilitation Stretching
Proprioceptive Neuromuscular Facilitation Stretching Group participants will undergo one session of PNF posterior shoulder stretching exercise in the modified sleeper position.
|
Among the PNF stretching techniques, the muscle-relaxation technique will be applied.
The athlete will be positioned in a side-lying posture on the treatment table with the dominant shoulder in the modified sleeper position, ensuring stabilization of the scapula on the table.
The other arm will be positioned in extension along the body with the palm facing upwards.
The participant will be instructed to actively bring the arm of the lower limb to the physiological barrier of internal rotation.
At this point, they will be asked to perform maximum isometric contraction in external rotation for 7 seconds.
After the isometric contraction, the muscle will be relaxed, and active-assisted stretching will be applied in internal rotation for 15 seconds.
A 5-second rest will be provided between repetitions, and the exercise will consist of 5 repetitions.
|
|
Experimental: The Percussive Massage Treatment
The Percussive Massage Treatment Group participants will receive a 5-minute massage on the posterior deltoid area.
|
In the group where regional vibration is applied, the Hypervolt™ vibrating massage device (HYPERICE Inc, US) will be used.
This device is a vibration device with five different speed settings, vibrating at 3,200 percussions per minute (HYPERICE Inc. 'Hypervolt' device.
Retrieved from https://hyperice.com/hypervolt-bluetooth,
Accessed on: 08.12.2021).
The device offers five different head attachment options.
For this study, the ball attachment option will be selected as it is the least aggressive option, and the vibration from the device will be applied to the relevant muscle body (Kayoda, 2019).
For facilitatory effect, the application will be performed on the posterior deltoid for 5 minutes at a low frequency.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Shoulder internal rotation range of motion
Time Frame: baseline measurements, 5 minutes and 30 minutes
|
Change of shoulder internal rotation range of motion (with a digital inclinometer)
|
baseline measurements, 5 minutes and 30 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Attack Speed
Time Frame: baseline measurements, 5 minutes and 30 minutes
|
Change of attack speed of the volleyball players (with a radar gun)
|
baseline measurements, 5 minutes and 30 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Sevgi Sevi Yeşilyaprak, PhD, Dokuz Eylul University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 10, 2024
Primary Completion (Actual)
May 1, 2024
Study Completion (Actual)
July 12, 2024
Study Registration Dates
First Submitted
March 5, 2024
First Submitted That Met QC Criteria
March 5, 2024
First Posted (Actual)
March 12, 2024
Study Record Updates
Last Update Posted (Actual)
July 15, 2024
Last Update Submitted That Met QC Criteria
July 12, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 7978-GOA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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