Digital Addiction Among University Students

NCT ID: NCT06584253

Last Updated: 2024-09-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

32 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-05-21

Study Completion Date

2024-09-12

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim of this study is to contribute to our understanding of digital media addiction by investigating the prevalence of digital addiction among university students and examining the relationship between variables such as body awareness, physical activity levels, hand grip strength, upper extremity function and pain-dash, quality of life, depression, stress, anxiety, sleep quality, and cognitive levels and digital addiction.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

After recording the demographic information of all individuals participating in the study, screen addiction, BMI, body awareness, physical activity levels, handgrip strength, upper extremity pain and function and pain-dash, quality of life, depression, stress, anxiety, sleep quality, cognitive levels will be evaluated. Individuals will be asked to fill out self-report questionnaires.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Internet Addiction University Student

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Musculoskeletal System Health Questionnaire Scale

It is a 14-item scale that evaluates pain intensity, physical function, sleep, fatigue, emotional state, physical activity level, impact on work and social life, independence, self-management ability and general impact.

Intervention Type OTHER

International Physical Activity Questionnaire (short form)

International Physical Activity Questionnaire (short form) -

The IPAQ assesses a range of physical activities, including leisure-time physical activities, indoor and outdoor activities, work-related physical activities, and transportation-related physical activities.

Intervention Type OTHER

Pittsburgh Sleep Quality Index

It is a questionnaire that evaluates sleep quality with questions asked under 7 main headings: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disorders, use of sleep aids and daytime functions.

Intervention Type OTHER

Cognitive Failures Questionnaire

The questionnaire aims to measure daily cognitive errors. It assesses simple errors made over the last 6 weeks, as well as perception (e.g., are there times when you can't see something you need at the supermarket even though it's there?), memory (e.g., have you ever forgotten people's names?) and motor functioning (e.g., have you ever bumped into anyone?).

Intervention Type OTHER

Jamar hand dynamometer

Jamar hand dynamometer - students will perform grip strength assessments with their dominant hand while seated. As recommended by the American Association of Hand Therapists protocol, students will sit in a comfortable chair with their shoulders neutrally rotated and adducted, elbow flexed to 90°, and wrist and forearm in neutral positions.

Intervention Type OTHER

Depression Anxiety Stress Scale - 21 Short Form

DASÖ-21 consists of 3 subcategories (depression, anxiety and stress). Each category consists of 7 separate questions and a total of 21 questions.

Intervention Type OTHER

Body Awareness Questionnaire

The questionnaire aims to determine the level of body composition sensitivity.

Intervention Type OTHER

SF-12

This questionnaire consists of two general components related to physical and mental function, consisting of 12 questions and 8 scales measuring physical function (2 questions), bodily pain (1 question), role limitations due to physical problems (2 questions), general health (1 question) vitality (40).

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* University students aged 18 and over
* Those who have been using smartphones for more than a year

Exclusion Criteria

* People under the age of 18,
* Those diagnosed by a doctor with any musculoskeletal, rheumatic, neurological, cardiovascular system diseases or diagnosed with a mental disorder, sleep disorder such as narcolepsy or addiction to alcohol, substances, etc.
* Those with any history of injury or surgery in the upper extremity
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Inonu University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

BÜŞRA CANDİRİ

PhD, physiotherapist, Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

dilan demirtas karaoba, asst. prof

Role: STUDY_DIRECTOR

Inonu University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Dilan Demirtas Karaoba

Iğdır, Iğdır, Turkey (Türkiye)

Site Status RECRUITING

Dilan

Iğdır, Iğdır, Turkey (Türkiye)

Site Status NOT_YET_RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

dilan demirtas karaoba, asst. prof

Role: CONTACT

0541127796

dilan demirtas karaoba, asst. prof

Role: CONTACT

05541127796

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

dilan demirtas karaoba, asst. prof

Role: primary

Büşra Candiri, asst. prof

Role: backup

burcu talu, prof

Role: backup

dilan demirtas karaoba

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2024/5922

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Effect of Smartphone Usage
NCT06941454 NOT_YET_RECRUITING