- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06079489
The Effect of Telerehabilitation-Based Structured Exercise Program in Video Game-Addicted Adults
October 6, 2023 updated by: Hikmet Ucgun, Biruni University
The increasing use of computers and mobile devices due to advancing technology has brought with it some negative consequences such as video game addiction.
Research has shown that playing video games for too long can lead to a number of acute and chronic serious musculoskeletal problems that can negatively affect health.
The aim of the present study is to investigate the effect of telerehabilitation-based structured exercise program in video game-addicted adults and compare these effects with the effect of brochure-based exercise.
Postural assessments, pain assessments, fine motor skill assessments, grip strength measurements, and reaction time assessments were performed.
All assessments were repeated before and after the 8-week program for both groups.
Participants in the EG were given a telerehabilitation-based structured exercise program for an average of 40 minutes three days a week for 8 weeks.
Participants in the CG were given brochure-based exercises three days a week for 8 weeks.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
44
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
-
-
-
Istanbul, Turkey, 34060
- Biruni 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
No
Description
Inclusion Criteria:
- Being between 18-40 years old
- Having a score of ≥30 on the Game Addiction Inventory for Adults (GAIA)
- Volunteering to participate in the study
- Having high-speed internet, a camera, and a microphone
Exclusion Criteria:
- Having a neurological/orthopedic condition that would prevent exercise
- Having a cognitive impairment
- Having a vision or hearing loss
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Control Group
Participants were advised to repeat the brochure-based exercises 3 days a week for 8 weeks.
Correct sitting and standing positions and ergonomic materials were also explained in detail.
Participants' adherence to the exercise program was tracked by an exercise diary.
|
Simple posture exercises
|
|
Experimental: Experimental Group
Progressive physical fitness and posture exercises were given via telerehabilitation 3 days a week for 8 weeks.
Specific exercises for upper extremities, lower extremities, neck, trunk and lower back were selected and progressed by changing the frequency, duration and variety within the program.
All exercises were performed under the supervision of a physiotherapist during video conference calls lasting an average of 40 minutes.
Correct sitting and standing positions and ergonomic materials were also explained in detail.
Participants' adherence to the exercise program was tracked by an exercise diary.
|
Progressive physical fitness and posture exercises
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Assessment
Time Frame: 1-2 minutes
|
The pain was assessed with the 10-cm VAS.
The participants used the VAS to make an assessment of their own pain, with 0 representing no pain, and 10 cm representing severe pain.
|
1-2 minutes
|
|
Fine Motor Skill Assessment
Time Frame: 4-5 minutes
|
The fine motor skill was assessed with the 9-Hole Peg Test.
It is a simple, fast test that requires minimal space and equipment and evaluates fine upper motor function.
In this test, the patient is asked to insert the pegs into the holes in the desired order and collect them back.
The duration of the test is measured by a specialist via a stopwatch.
|
4-5 minutes
|
|
Posture Assessment
Time Frame: 5-10 minutes
|
Posture was assessed with the PostureZone Posture Application.
The PostureZone mobile application, which can be downloaded free of charge on both Android and iOS via smartphone, will be used to evaluate the static postures of the participants.
It is an application developed for clinicians that assess static posture.
The participant is photographed with minimal clothing on, certain pivot points are marked, and the deviations of these points relative to the vertical-horizontal planes are determined.
|
5-10 minutes
|
|
Hand Reaction Assessment
Time Frame: 10-15 minutes
|
Hand Reaction was assessed with the Nelson Hand Reaction Test.
The participant sits on a chair with his forearm and hand in a comfortable position on the table.
The tester holds the end of the ruler.
The participant is asked to catch the ruler.
Twenty rials are performed.
The lowest 5 and highest 5 attempts are discarded and the average of the remaining 10 attempts is recorded as the result.
|
10-15 minutes
|
|
Handgrip Strength Assessment
Time Frame: 4-5 minutes
|
Jamar Hydraulic Hand Dynanometer was used to assess handgrip strength.
Each trial was repeated three times and the average was recorded in kilograms
|
4-5 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
February 1, 2023
Primary Completion (Actual)
October 1, 2023
Study Completion (Actual)
October 1, 2023
Study Registration Dates
First Submitted
October 6, 2023
First Submitted That Met QC Criteria
October 6, 2023
First Posted (Actual)
October 12, 2023
Study Record Updates
Last Update Posted (Actual)
October 12, 2023
Last Update Submitted That Met QC Criteria
October 6, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- buhucgun03
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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