- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06403384
Vibration Therapy in Wheelchair Basketball Players
May 3, 2024 updated by: MERT UYSAL, Karabuk University
Effects of Vibration Therapy on Muscle Soreness and Athletic Performance in Wheelchair Basketball Players
No study was found that investigated the effect of vibration therapy (VT) on recovery from exercise in WCB players.
Therefore, the aim of the study was to investigate the effects of wearable local vibration device on muscle soreness and athletic performance during recovery from exercise in the elbow area in WCB players.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Vibration therapy (VT) has been widely used to increase performance and rehabilitate injuries in athletes.
Delayed onset muscle soreness (DOMS), caused by excessive overload after training and competitions, leads to loss of performance.
The aim of this study was to investigate the effects of wearable local VT on muscle soreness and athletic performance in wheelchair basketball (WCB) players.
Study Type
Interventional
Enrollment (Actual)
13
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
-
-
-
Karabük, Turkey
- Karabuk U
-
-
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
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Being a wheelchair basketball players
Exclusion Criteria:
- Having had an upper extremity operation within the last 6 months
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: Non-Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
no intervention was applied for the control group
|
|
|
Experimental: Vibration
Vibration was applied for the vibration group
|
Local vibration was applied
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle Soreness
Time Frame: pre-exercise (baseline), and 30 minutes and 24 hours post-exercise
|
Muscle soreness was evaluated for both arms of the athletes with the "Numeric Pain Scale".
This scale is horizontally scored between 0-10 (0 = no pain, 10 = unbearable pain).
|
pre-exercise (baseline), and 30 minutes and 24 hours post-exercise
|
|
Shooting percentage
Time Frame: pre-exercise (baseline), and 30 minutes and 24 hours post-exercise
|
The participants were asked to shoot 10 free throws in total from the free throw line with the wheelchair after a warmup.
The percentage of successful throws was accepted as the shooting percentage value of the athletes (number of successful throws x 100 / total number of throws).
|
pre-exercise (baseline), and 30 minutes and 24 hours post-exercise
|
|
20-meter sprint test
Time Frame: pre-exercise (baseline), and 30 minutes and 24 hours post-exercise
|
For the test, a 20-meter track was created on the basketball court floor, and 2 meters were added to the distance and marked so that the athletes would not slow down on the last meters.
The time to complete the 20-meter track with the ready and start command of the participants was recorded with a stopwatch.
|
pre-exercise (baseline), and 30 minutes and 24 hours post-exercise
|
|
Joint position sense
Time Frame: pre-exercise (baseline), and 30 minutes and 24 hours post-exercise
|
Joint position sense was evaluated with the passive to active joint repositioning method using a digital inclinometer device.
The participants sat with the elbow extended and eyes closed on their wheelchairs.
The target angles were selected 30°, 60° and 90° of the elbow joint.
|
pre-exercise (baseline), and 30 minutes and 24 hours post-exercise
|
|
Range of motion
Time Frame: pre-exercise (baseline), and 30 minutes and 24 hours post-exercise
|
Both elbow joint extension/flexion angles were measured with a universal goniometer (baseline) with the arm in anatomical position on the wheelchair.
|
pre-exercise (baseline), and 30 minutes and 24 hours post-exercise
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Mert Uysal, Karabuk 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)
August 1, 2021
Primary Completion (Actual)
April 1, 2022
Study Completion (Actual)
August 1, 2022
Study Registration Dates
First Submitted
April 30, 2024
First Submitted That Met QC Criteria
May 3, 2024
First Posted (Actual)
May 7, 2024
Study Record Updates
Last Update Posted (Actual)
May 7, 2024
Last Update Submitted That Met QC Criteria
May 3, 2024
Last Verified
May 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- KBU-FTR-MU-01
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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