LACHETONPHONE : Impact of a Dedicated Consultation Using a Structured Interview Guide on Screen Time Among Adolescents Aged 12 to 17 in Primary Care

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age12-17
SponsorUniversity Hospital, Strasbourg, France

About this trial

Adolescents spend a large amount of time on screens, especially smartphones. Excessive screen use has been linked to health problems such as poor sleep, reduced physical activity, academic difficulties, and mental health issues. Primary care professionals often lack practical tools to help young people address this problem.

This study aims to evaluate whether a dedicated medical consultation (DC), using a structured interview guide and a screening questionnaire (e-KID), can help adolescents aged 12 to 17 reduce and improve their screen use. When excessive screen exposure is identified, adolescents are offered a personalized consultation with a healthcare professional. Together, they discuss screen habits, health impacts, and set achievable goals to change usage patterns.

The investigator hypothesizes that adolescents who receive this dedicated consultation by healthcare providers trained with a specific grid will better reduce their smartphone screen time and adopt healthier screen use habits compared to those receiving usual care.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adolescent aged 12 to 17 years at the time of enrolment (participants aged 17 must not have turned 18 on the day of inclusion).

Adolescent owning a smartphone, with usage >14 hours/week and a score >10/21 on the early overexposure screening questionnaire (e-KID).

Adolescent and parent(s) or legal guardian(s) able to understand the objectives of the research.

Adolescent whose parent(s) or legal guardian(s) have signed an electronic informed consent (e-Consent) prior to any study-related procedures.

Disqualifiers

Adolescent with severe psychiatric disorders (DSM-V diagnosis and/or treatment with amphetamines, neuroleptics, or psychotropic drugs).

Adolescent currently excluded from participation due to a previous or ongoing study.

Adolescent under legal guardianship or conservatorship (tutelle or curatelle).

Adolescent female who is pregnant or breastfeeding (self-reported).

Trial design

Design model

Parallel

Treatments tested in this trial

  • Structured Interview Guide

    Behavioral

    a dedicated consultation with a structured interview guide

  • Standard practice about screen use prevention for adolescents

    Behavioral

    Standard practice

Treatment groups

400 Participants
are divided into 2 treatment groups
Group A: Control: Standard PracticeOther 1 intervention
Group B: Experimental: Structured Interview GuideExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in time spent on the smartphone, measured in hours and minutes (recorded via screenshots), between the baseline visit and one month later, over a period of 7 consecutive days and outside school holidays, in both groups.

Change in time spent on smartphone use, measured in hours and minutes, assessed via participant screenshots of screen-time statistics. Smartphone use will be recorded over 7 consecutive consecutive days at each time point (baseline and 1 month), excluding school holidays, in both intervention and control groups.

Time frame
At Baseline and 1-month follow-up (7 consecutive days of measurement at each time point, excluding school holidays)

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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