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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06403384
Other study ID # KBU-FTR-MU-01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 1, 2021
Est. completion date August 1, 2022

Study information

Verified date May 2024
Source Karabuk University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 13
Est. completion date August 1, 2022
Est. primary completion date April 1, 2022
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Being a wheelchair basketball players Exclusion Criteria: - Having had an upper extremity operation within the last 6 months

Study Design


Intervention

Device:
Vibration
Local vibration was applied

Locations

Country Name City State
Turkey Karabuk U Karabük

Sponsors (1)

Lead Sponsor Collaborator
Karabuk University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle Soreness 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
Primary Shooting percentage 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
Primary 20-meter sprint test 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
Primary Joint position sense 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
Primary Range of motion 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
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