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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05345535
Other study ID # 2022/033
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 18, 2022
Est. completion date October 30, 2022

Study information

Verified date April 2022
Source Hasan Kalyoncu University
Contact Elif Dinler, Master degree
Phone +905314920222
Email elif.dokunlu@hku.edu.tr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date October 30, 2022
Est. primary completion date July 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 65 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Trampoline exercise
45 minutes of exercises that includes upper and lower extremity movements a trampoline with music
Walking
45 minutes of moderate tempo walking

Locations

Country Name City State
Turkey Hasan Kalyoncu University Gaziantep

Sponsors (1)

Lead Sponsor Collaborator
Hasan Kalyoncu University

Country where clinical trial is conducted

Turkey, 

Outcome

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