Acute Effects of Trampoline Exercises

April 25, 2022 updated by: Elif Dinler, Hasan Kalyoncu University

Investigation of the Acute Effects of Trampoline Exercises on Balance, Proprioception, Vertical Jump and Cognitive Functions

The aim of the study is to investigate the acute effects of trampoline exercises on balance, proprioception, vertical jump and cognitive functions. As a result of the study, it is thought that trampoline exercises will affect balance, proprioception, vertical jump, cognitive functions and myotonometric properties of the muscle more positively than walking.

Study Overview

Status

Not yet recruiting

Detailed Description

30 healthy, volunteer women who meet the inclusion criteria will be included in the study. Participants will be divided into two group randomly. The women in the study group will be evaluated before the first trampoline exercise sessions and the acute effect will be evaluated by re-evaluating at the end of the 45-minute (min) session. The control group women will be evaluated and after 45 minutes of walking, they will be evaluated again for the acute effect over the relevant parameters. The evaluations to be made to the participants are given below;

  • Demographic Information Form (Age, height (cm), weight (kg), occupation, education level, previous and present diseases, smoking, etc.)
  • Balance Evaluation - Y Balance Test
  • Ankle joint position sense - Electrogoniometer
  • Cognitive assessment - Stroop test
  • Vertical jump test - tape measure
  • Myotonometric properties of gastrocnemius, tibialis anterior and peroneal muscles- Myoton device

Study Type

Interventional

Enrollment (Anticipated)

30

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 Contact

Study Locations

      • Gaziantep, Turkey, 27100
        • Hasan Kalyoncu University
        • Contact:

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

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Females who agreed to participate in the study voluntarily,
  • Female individuals between the ages of 18-65 years old
  • Females who have mini mental test score more than 25

Exclusion Criteria:

  • Those with a Body Mass Index (BMI) greater than 30 kg/m²,
  • Pregnant women,
  • Those with following problems; neural findings, malignancy, inflammation, arthritis, metabolic bone disease, column vertebralis or lower extremity surgery, cardiovascular system diseases, severe osteoporosis, communication and hearing disorders, chronic diseases such as diabetes, hypertension,
  • Those who illiterate,
  • Individuals who do sports for more than 150 minutes a week,
  • Individuals with a professional sports background, Individuals who do sports for more than 150 minutes a week
  • Individuals with a professional sports background

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: Diagnostic
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Study group
Participants of study group will perform 45 minutes of trampoline exercises. Evaluations are going to be done immediately before and after trampoline session.
45 minutes of exercises that includes upper and lower extremity movements a trampoline with music
Experimental: Control group
Participants of control group will perform 45 minutes of walking. Evaluations are going to be done immediately before and after walking session.
45 minutes of moderate tempo walking

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in Y balance test score
Time Frame: Immediately after the intervention
Balance score is going to be assess by Y balance test to determine change from baseline.
Immediately after the intervention
Change from baseline in ankle position sense degree
Time Frame: Immediately after the intervention
Ankle position sense degree is going to be assess by electroconiometer to determine change from baseline.
Immediately after the intervention
Change from baseline in vertical jump distance
Time Frame: Immediately after the intervention
Vertical jump distance (centimeter) is going to be assess by vertical jump test by a tape measure.
Immediately after the intervention
Change from baseline in myotonometric characteristics
Time Frame: Immediately after the intervention
Myotonometric characteristic is going to be assess by MyotonPRO device.
Immediately after the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in cognitive status
Time Frame: Immediately after the intervention
Cognitive status is going to be assess by Stroop Test. Correct and false answers will be record. More correct answer shows higher cognitive status.
Immediately after the intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 (Anticipated)

April 18, 2022

Primary Completion (Anticipated)

July 30, 2022

Study Completion (Anticipated)

October 30, 2022

Study Registration Dates

First Submitted

April 19, 2022

First Submitted That Met QC Criteria

April 25, 2022

First Posted (Actual)

April 26, 2022

Study Record Updates

Last Update Posted (Actual)

April 26, 2022

Last Update Submitted That Met QC Criteria

April 25, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 2022/033

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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