- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07442955
Impact of Digital Muscle Strength on Activity in Tech-Addicted University Students
The Effect of Digital Muscle Strength Measurement on Physical Activity Levels in University Students With Technological Addiction
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
-
Samsun, Turkey (Türkiye)
- Ondokuz Mayıs University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Be between the ages of 18 and 30
- Be a university student
- Have no physical or systemic illnesses that would prevent you from working
Exclusion Criteria:
- Not being between the ages of 18 and 30
- Not being a university student
- Having a physical or systemic illness that prevents working
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Students with Digital Addiction
|
Evaluation of muscle strength, Young Internet Addiction Test-Short Form (YIAT-SF), International Physical Activity Questionnaire-Short Form (IPAQ-SF) and SF-12
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lafayette Muscle Strength Devices
Time Frame: 1 year
|
The Lafayette muscle strength measurement device is a digital dynamometer used to objectively and numerically assess maximum isometric muscle strength.
The device provides a more precise and repeatable measurement than manual muscle testing, providing a reliable method for assessing muscle strength.
It can be used with various attachments for different muscle groups and is frequently used in rehabilitation, performance analysis, and clinical research.
A high score indicates high muscle strength.
|
1 year
|
|
International Physical Activity Questionnaire - Short Form (IPAQ-SF)
Time Frame: 1 year
|
The IPAQ-SF is an internationally standardized self-report questionnaire developed to determine individuals' physical activity levels.
This seven-question short form assesses **walking, moderate-intensity, and vigorous-intensity physical activities**, as well as **sitting time**, over the past seven days.
Using participant-reported duration and frequency data, physical activity level is calculated in **MET-minutes/week**.
Its rapid administration and applicability to large populations make it a valid and reliable measurement tool for population-based research and clinical trials.
Participants can use physical activity levels of Low, Moderate, or High based on their MET score, depending on the day and time.
A higher MET value indicates a higher level of physical activity.
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of Life (SF-12)
Time Frame: 1 year
|
Quality of Life will assess with SF-12. The SF-12 is a short self-report questionnaire developed to assess individuals' general health status and quality of life. A shortened version of the SF-36, this scale consists of 12 questions and assesses physical and mental health components (Physical Component Summary (PCS) and Mental Component Summary (MCS). Due to its short administration time and practicality, it is frequently used in clinical research, community health studies, and rehabilitation. A high score indicates a high level of life quality. Scores range from 0 to 100. 0 points: Worst health status and 100 points: Best health status. Higher scores indicate better physical or mental health. Lower scores indicate worse health status. |
1 year
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023/437
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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