Investigation of the Acute Effects of Percussive Massage Treatment and Stretching Exercise on Balance and Performance

Sponsor
Istanbul Medipol University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT05192070
Collaborator
(none)
48
1
3
1.2
40.6

Study Details

Study Description

Brief Summary

In this study, it was aimed to investigate the acute effects of Percussion Massage Therapy and stretching exercises on balance, horizontal jumping and performance in healthy individuals. It was planned to include 45 individuals in the study. Participants will be randomly divided into 3 groups. Horizontal jumping distance, T-Drill test and balance assessment will be done for all participants. After the evaluation, percussion massage therapy will be given to the 1st group, dynamic stretching exercises to the 2nd group, and static stretching exercises to the 3rd group. All measurements will be repeated after the intervention.

Condition or Disease Intervention/Treatment Phase
  • Other: Percussive Massage Group
  • Other: Dynamic stretching group
  • Other: Static stretching group
N/A

Detailed Description

48 healthy individuals meeting the inclusion criteria of Istanbul Medipol University will be included in the study. Individuals who are at a level to perform performance tests, who have not undergone orthopedic surgery in any of their regions, who do not have problems in running and during sudden turns, and who do not have a professional sports background will be included in the study. Individuals with a history of trauma, anatomical deformities and skeletal system fractures, diagnosed orthopedic or rheumatological diseases, being included in the physiotherapy program in the last 6 months, and those with pain in any region will be excluded from the study. Before the study, demographic information, horizontal jump test, T-Test and Fizyosoft balance system will be evaluated with both feet and one foot with eyes open and closed. After the evaluation, percussion massage therapy will be given to the 1st group, dynamic stretching exercises to the 2nd group, and static stretching exercises to the 3rd group. All measurements will be repeated after the intervention.

Study Design

Study Type:
Interventional
Actual Enrollment :
48 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Masking Description:
Participants will not know which groups they belongs to
Primary Purpose:
Treatment
Official Title:
Investigation of the Acute Effects of Percussive Massage Treatment and Stretching Exercise on Balance and Performance
Actual Study Start Date :
Jan 25, 2022
Actual Primary Completion Date :
Feb 20, 2022
Actual Study Completion Date :
Mar 2, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Percussive Massage Group

Quadriceps, hamstring and gastrocnemius muscles of the participants will done massage for 3 minutes with a hypervolt massage device.

Other: Percussive Massage Group
Quadriceps, hamstring and gastrocnemius muscles of the participants will done massage for 3 minutes with a hypervolt massage device.

Experimental: Dynamic stretching group

Dynamic stretching will be performed for the quadriceps, hamstring and gastrocnemius muscles of the participants with 10 repetitions.

Other: Dynamic stretching group
Dynamic stretching will be performed for the quadriceps, hamstring and gastrocnemius muscles of the participants with 10 repetitions.

Experimental: Static stretching group

Static stretching will be performed for the quadriceps, hamstring and gastrocnemius muscles of the participants with 10 repetitions.

Other: Static stretching group
Static stretching will be performed for the quadriceps, hamstring and gastrocnemius muscles of the participants with 10 repetitions.

Outcome Measures

Primary Outcome Measures

  1. Horizontal jumping test [2 minutes]

    The starting line is drawn on a flat surface. A tape measure is placed on the floor from the starting line forward and the athletes are asked to take a position with the tips of both toes pointing towards the back of the previously determined line. The distance jumped is measured in cm after the athletes are asked to have their knees bent while their arms are parallel to the floor and knees, and to jump forward as much as possible by swinging their arms and legs quickly.

  2. T drills test [3 minutes]

    It consists of a 9.14 meter forward sprint, 4.57 meter side step to the left, 9.14 meter slide step to the right, 4.57 meter side step to the left, and 9.14 meter backward steps. From the starting point, before starting the run, the individuals are told to take a forward bending motion for at least 3 seconds. The results of the measurement are recorded in seconds. The best score in three attempts will be recorded.

  3. BecureBalance measurement [10 minutes]

    Fizyosoft Becure Balance System balance evaluation protocol will be evaluated as 30 seconds of two-foot balance with eyes open and closed, and 30 seconds of balance with one foot with eyes open and closed.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 25 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Capable of performing performance tests

  • Those who have not undergone orthopedic surgery in any region

  • Having no problems during running and sudden turns

  • Individuals who do not have a professional sports background

Exclusion Criteria:
  • Trauma history

  • Anatomical deformities and skeletal system fractures

  • Diagnosed orthopedic or rheumatological diseases

  • Being included in a physiotherapy program in the last 6 months

  • Individuals with pain in any part of the study

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istanbul Medipol University Istanbul Turkey 34820

Sponsors and Collaborators

  • Istanbul Medipol University Hospital

Investigators

  • Principal Investigator: Burak Menek, Medipol University

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
burak menek, Principal Investigator, Istanbul Medipol University Hospital
ClinicalTrials.gov Identifier:
NCT05192070
Other Study ID Numbers:
  • bmenek.
First Posted:
Jan 14, 2022
Last Update Posted:
Mar 3, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by burak menek, Principal Investigator, Istanbul Medipol University Hospital

Study Results

No Results Posted as of Mar 3, 2022