Assessment and Characterization of Sleep Among Video Game Adult Players Without Video Game Use Disorder : a Feasability Study
Condition(s) studied
Investigational drug(s) / intervention(s)
Sleep Assessment Protocol: Participants will engage in a structured protocol to assess sleep patterns and potential disturbances related to video game usage. This protocol includes: * Completion of diaries: Participants will maintain a sleep diary, video game usage diary, and screen time diary for 14 days to record their activities and sleep quality. * Clinical assessments: At Visit 2, participants will complete questionnaires related to sleep quality and disturbances, administered by a sleep specialist neurologist. * Actigraphy monitoring: Participants will wear an actimeter during the 14-day recording period to objectively measure sleep activity. * Biological sampling: After the 14 days, participants will provide urinary samples for analysis of 6-sulfatoxymelatonin to evaluate melatonin levels.
Study summary
The primary objective of the SLEEPLAY study is to assess the feasibility of a research protocol investigating the impact of video games on sleep in adults. More specifically, this study aims to identify potential barriers, facilitators of participation, and participant adherence to various measurement tools (such as actigraphy and melatonin assays) to validate the protocol for a larger future study. Additionally, it seeks to optimize the recruitment of regular adult gamers and determine the conditions that will enable better collection of objective sleep data. The relevance of this feasibility study lies in its ability to test and refine the methodology, thereby facilitating future research while minimizing costs and implementation time.
Eligibility
Primary outcome measure(s)
- Recruitment Capacity — Month 20 of the study
Number of participants successfully included in the study per month within each group (Regular Gamers and Non-Gamers). - Attrition rate — Month 21 at the end of the study
Percentage of participants who drop out of the study. - Data Completeness — Month 21 at the end of the study
Mean number of days with valid data for: sleep diary, video game and screen-use diary, actigraphy (≥90% wear time), urinary samples for 6-sulfatoxymelatonin - Acceptability — Month 20 of the study
Proportion of subjects who accepted to participate in the study compared to the number of eligible patients contacted.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| CHU de Besançon | Besançon | France | Recruiting |
More Centre Hospitalier Universitaire de Besancon trials in France
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07411404 on ClinicalTrials.gov ↗ ← All trials in France