- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06396936
The Effect of Calisthenic Exercises
December 2, 2024 updated by: KTO Karatay University
Investigation of the Effects of Physical Activity on Smartphone Addiction, Pain and Sleep Quality in Young Adults
This study will investigate the effects of physical activity in young adults.
With the increase in physical activity, the change in smartphone addiction, pain and sleep quality parameters will be evaluated.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study aims to increase physical activity with a calisthenic exercise program.
An answer will be sought to the question of whether increased physical activity causes changes in phone addiction, pain and sleep quality parameters.
Study Type
Interventional
Enrollment (Actual)
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
-
-
-
Konya, Turkey
- KTO Karatay 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
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Volunteering to participate in the study.
- Being between the ages of 15-35.
Exclusion Criteria:
- Individuals with an orthopedic and/or neurological disease that will affect their sleep health and/or pain level,
- Individuals with physical disabilities,
- Individuals who have undergone any surgical procedure in the last 6 months.
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control Group
No intervention
|
|
|
Experimental: Study Group
Calisthenic exercise program
|
Calisthenic exercises to be applied in our study; These are exercises that are performed by creating resistance only with your body weight, without the need for any equipment or gym.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sleep Quality
Time Frame: The evaluation will be applied at the beginning of the treatment program.
|
Pittsburgh Sleep Quality Index will used to evaluate overall sleep quality in young adults.
|
The evaluation will be applied at the beginning of the treatment program.
|
|
Smartphone addiction
Time Frame: The evaluation will be applied at the beginning of the treatment program.
|
The short version of the smartphone addiction scale (SAS-SV) will used to evaluate smartphone addiction.
|
The evaluation will be applied at the beginning of the treatment program.
|
|
Physical Activity
Time Frame: The evaluation will be applied at the beginning of the treatment program.
|
The International Physical Activity Survey will used to evaluate physical activity.
|
The evaluation will be applied at the beginning of the treatment program.
|
|
Levels of Quality of life
Time Frame: The evaluation will be applied at the beginning of the treatment program.
|
Short Form Health Survey (SF-36) will used to evaluate health status.
|
The evaluation will be applied at the beginning of the treatment program.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain intensity (neck pain and head pain)
Time Frame: The evaluation will be applied at the beginning of the treatment program
|
The Visual Analogue Scale (VAS) will used to measure pain intensity.
|
The evaluation will be applied at the beginning of the treatment program
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Osman Karaca, PhD, KTO Karatay University
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)
May 7, 2024
Primary Completion (Actual)
May 10, 2024
Study Completion (Actual)
July 12, 2024
Study Registration Dates
First Submitted
April 30, 2024
First Submitted That Met QC Criteria
April 30, 2024
First Posted (Actual)
May 2, 2024
Study Record Updates
Last Update Posted (Estimated)
December 4, 2024
Last Update Submitted That Met QC Criteria
December 2, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KTOKARACA002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Individual participant data is not sharing other researchers.
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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