- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07541963
Investigation of the Effect of Screen Time Before Sleep on Posture Disorders and Dynamic Balance
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Postural disorders arise from the disruption of the natural alignment of the spine and are often associated with muscle imbalances, joint stress, and pain. Incorrect posture caused by prolonged technology use has been reported to increase the risk of musculoskeletal problems among young adults.
Dynamic balance is an important component of postural control and is influenced by the integration of sensory input and neuromuscular responses. Sleep disturbances and lifestyle habits, including excessive screen exposure before sleep, may affect this complex system.
Therefore, the aim of this study is to investigate the effect of screen time before sleep on posture disorders and dynamic balance in healthy young adults. Participants aged between 18 and 35 years will be evaluated for screen usage habits before sleep. Posture analysis and the Star Excursion Balance Test will be used to assess posture alignment and dynamic balance performance.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Esra Pehlivan
- Phone Number: 0 216 777 8 777
- Email: esra.pehlivan@sbu.edu.tr
Study Contact Backup
- Name: Rumeysa Yanak
- Phone Number: 02167779600
- Email: rumeysayanakk@gmail.com
Study Locations
-
-
Üsküdar
-
Istanbul, Üsküdar, Turkey (Türkiye), 34668
- Saglik Bilimleri Universitesi
-
Contact:
- Esra Pehlivan, Associate Professor
- Phone Number: 02164189616
- Email: fztesrakambur@yahoo.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Healthy adults
- Aged 18 to 35 years
- Willing to participate voluntarily in the study
Exclusion Criteria:
- History of orthopedic injury or surgery affecting balance
- Use of medications that may affect attention or balance
- Refusal to provide informed consent
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy young individuals with pre-sleep screen exposure
34 healthy volunteers between the ages of 18-35 were included in the study.
Participants are assessed for screen exposure before sleep, posture disorders, and dynamic balance.
|
Pre-sleep screen exposure is evaluated using smartphone-based self-reported queries on duration and usage characteristics
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Posture Analysis
Time Frame: Single assessment at baseline
|
Evaluation of body alignment including head position, shoulder alignment, spinal curvature, pelvic position, knee alignment, and foot posture from anterior, posterior, and lateral views.
|
Single assessment at baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Star Excursion Balance Test
Time Frame: Single assessment at baseline
|
Dynamic balance performance will be assessed by measuring the maximum reach distance in eight directions while maintaining single-leg stance.
|
Single assessment at baseline
|
|
Duration of pre-sleep screen exposure
Time Frame: Single assessment at baseline
|
The duration of screen exposure within 1 hour before bedtime will be assessed using self-report and recorded in minutes.
Higher values indicate longer screen exposure before sleep.
|
Single assessment at baseline
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
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
Other Study ID Numbers
- Sleep&ScreenTime1
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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