NCT06403384

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
13

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Aug 2021

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2021

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2022

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2022

Completed
1.7 years until next milestone

First Submitted

Initial submission to the registry

April 30, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

May 7, 2024

Completed
Last Updated

May 7, 2024

Status Verified

May 1, 2024

Enrollment Period

8 months

First QC Date

April 30, 2024

Last Update Submit

May 3, 2024

Conditions

Keywords

AthleteDisabled personsExercisePainProprioceptionUpper extremity

Outcome Measures

Primary Outcomes (5)

  • 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

  • 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

  • 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

  • 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

  • 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

Study Arms (2)

Control

NO INTERVENTION

no intervention was applied for the control group

Vibration

EXPERIMENTAL

Vibration was applied for the vibration group

Device: Vibration

Interventions

VibrationDEVICE

Local vibration was applied

Vibration

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Being a wheelchair basketball players

You may not qualify if:

  • Having had an upper extremity operation within the last 6 months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Karabuk U

Karabük, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Motor ActivityPain

Condition Hierarchy (Ancestors)

BehaviorNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Mert Uysal

    Karabuk University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

April 30, 2024

First Posted

May 7, 2024

Study Start

August 1, 2021

Primary Completion

April 1, 2022

Study Completion

August 1, 2022

Last Updated

May 7, 2024

Record last verified: 2024-05

Data Sharing

IPD Sharing
Will not share

Locations