- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05345535
Acute Effects of Trampoline Exercises
Investigation of the Acute Effects of Trampoline Exercises on Balance, Proprioception, Vertical Jump and Cognitive Functions
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Elif Dinler, Master degree
- Phone Number: +905314920222
- Email: elif.dokunlu@hku.edu.tr
Study Locations
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-
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Gaziantep, Turkey, 27100
- Hasan Kalyoncu University
-
Contact:
- Elif Dinler, Master degree
- Phone Number: +905314920222
- Email: elif.dokunlu@hku.edu.tr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2022/033
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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