- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06949371
Investigation of the Effects of Chronotype Differences on Balance and Muscle Strength in Young Adults (Chronotype)
May 26, 2025 updated by: merve yilmaz menek, Istanbul Medipol University Hospital
The aim of this study is to investigate the effects of chronotype differences on balance and muscle strength in young adults.
Chronotypes of all participants will be determined using the Morningness-Eveningness Questionnaire.
All assessment measurements determined for young adult individuals will be performed first at 09:00 in the morning and then again at 19:00 in the evening.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
The aim of this study is to investigate the effects of chronotype differences on balance and muscle strength in young adults.
Inclusion criteria are being between 45-65 years old, not having any neurological or orthopedic disorders, not having a vestibular disease that causes balance problems.
Exclusion criteria are trauma history, anatomical deformities and skeletal system fractures, having a previous injury, and the presence of pain that will prevent participation in the tests.
Chronotypes of all participants will be determined using the Morningness-Eveningness Questionnaire.
All assessment measurements determined for young adult individuals will be performed first at 09:00 in the morning and then again at 19:00 in the evening.
Muscle strength and balance assessments made in the morning and evening will be compared.
Chronotypes of the participants will be evaluated with the Morningness-Eveningness Questionnaire, their balance will be evaluated with the One-Legged Standing Test, lower extremity muscle strength with a myometer, and their functionality will be evaluated with the Timed Stand-Up-Sit Test and the 30-Second Sit-Up Test.
Study Type
Interventional
Enrollment (Estimated)
40
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 Locations
-
-
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Istanbul, Turkey
- İstanbul Medipol University
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- being between 45-65,
- not having any neurological or orthopedic disorder,
- not having a vestibular disease that causes balance problems.
Exclusion Criteria:
- trauma history,
- anatomical deformities and skeletal system fractures,
- having a previous injury and the presence of pain that would prevent participation in the tests.
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Morning chronotype group
All assessment measurements determined for individuals with morning chronotype will be performed first at 09:00 in the morning and then again at 19:00 in the evening.
|
All assessment measurements determined for individuals with morning chronotype will be performed first at 09:00 in the morning and then again at 19:00 in the evening.
Muscle strength balance assessments performed in the morning and evening will be compared.
|
|
Experimental: Evening chronotype group
All assessment measurements determined for individuals with evening chronotype will be performed first at 09:00 in the morning and then again at 19:00 in the evening.
|
All assessment measurements determined for individuals with evening chronotype will be performed first at 09:00 in the morning and then again at 19:00 in the evening.
Muscle strength balance assessments performed in the morning and evening will be compared.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Morningness-Eveningness Questionnaire
Time Frame: 20 minutes
|
A questionnaire form that determines morningness and eveningness types will be used to subjectively evaluate circadian rhythm.
defi - nitely morning type (70-86), moderately morning type (59-69), neither type (42-58), moderately evening type (31-41), and defi nitely evening type (16-30).
|
20 minutes
|
|
Single-leg standing test
Time Frame: 20 minutes
|
This test measures a person's standing ability and balance.
|
20 minutes
|
|
Muscle strength test
Time Frame: 20 minutes
|
Myometry will be used to objectively measure the strength of the quadriceps and hamstring muscles.
Myometry is an evaluation method that objectively evaluates muscle strength and provides more sensitive results than manual muscle testing.
|
20 minutes
|
|
Timed up and go testTest:
Time Frame: 20 minutes
|
A simple screening test that provides a sensitive and specific measure of fall risk and balance in older adults.
|
20 minutes
|
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30 Second Sit-to-Stand Test
Time Frame: 20 minutes
|
A test that evaluates the participant's sit-to-stand activity, lower extremity muscle strength and balance status.
|
20 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: MERVE YILMAZ MENEK, Assoc. Prof., Medipol University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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 (Actual)
April 22, 2025
Primary Completion (Estimated)
June 10, 2025
Study Completion (Estimated)
July 10, 2025
Study Registration Dates
First Submitted
April 22, 2025
First Submitted That Met QC Criteria
April 22, 2025
First Posted (Actual)
April 29, 2025
Study Record Updates
Last Update Posted (Actual)
May 30, 2025
Last Update Submitted That Met QC Criteria
May 26, 2025
Last Verified
May 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- E-10840098-772.02-7691
- Istanbul Medipol University (Other Identifier: Istanbul Medipol University Ethics Committee Decision No: 855/2021)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
We can share IPD when it isi necessary.
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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