This study evaluates the effects of a digital detox program on screen time, sleep quality, and healthy lifestyle behaviors among adolescents aged 10-19 years. Excessive use of smartphones and digital devices is associated with poor sleep quality, reduced well-being, and impaired daily functioning.
Participants will be randomly assigned to either a digital detox intervention group or a control group. The intervention consists of ten weekly 60-minute sessions designed to reduce screen time, increase awareness of digital media use, and improve sleep hygiene. The control group will not receive any intervention.
Data will be collected at baseline and approximately 10 weeks after the intervention using standardized questionnaires and screen time measures. The study aims to evaluate whether a structured digital detox program improves behavioral and sleep-related outcomes in adolescents.
Who can participate
Age range
10 Years – 19 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria Aged 10-19 years Smartphone user At least 3 hours of daily screen time Willing to participate in the digital detox program Written informed consent and parental consent obtained No diagnosed chronic medical condition or sleep disorder Exclusion Criteria Outside the age range (10-19 years) Does not use a smartphone Daily screen time less than 3 hours Diagnosed chronic medical illness (e.g., diabetes, asthma, epilepsy) Diagnosed sleep disorder Current psychiatric treatment or medication use Previous participation in a similar digital detox or sleep intervention Unable to attend intervention sessions regularly Refusal to complete study assessments
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Changes in Multi-Screen Addiction Levels
Timeframe: Baseline and approximately 10 weeks post-intervention