Life sciences · Interventional Study
ClinicalTrials.gov · October 23, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Interventional Study.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT07892807). This is a study registration, not published results. Lead sponsor: Brown University. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 40 participants (ESTIMATED). Conditions: Depression and/or Anxiety Symptoms, Problematic Phone Use Behavior. Interventions: BEHAVIORAL: Mindwire. Primary outcome measures: Study Recruitment Feasibility as Measured by Participant Recruitment Rates , During recruitment period of study, up to 3 months; Study Retention Feasibility as Measured by Participant Retention Rates , Baseline, Post-intervention (day 18), and 2-month Follow-up; Intervention Engagement Feasibility as Measured by Participant Engagement with Intervention , During intervention period (18 days); Intervention Acceptability as Measured by Client Satisfaction Questionnaire (CSQ-8) , Post-intervention (day 18); Intervention Acceptability as Measured by Session Evaluation Form , Post-intervention (day 18). Brief summary: The goal of this clinical trial is to understand the feasibility and acceptability on a mindfulness-based intervention to address co-existing smartphone addiction and psychological distress among adolescents ages 13-19 self-reporting elevated levels of depression and/or anxiety symptoms and problematic digital phone use. The main questions it aims to answer are: (1) is Mindwire, a mindfulness-based intervention, feasible and acceptable in addressing co-existing smartphone addiction and psychological distress among adolescents; and (b) what are the mechanistic pathways, particularly the role of circadian rhythm, sleep quality, and emotion regulation, in phone use and psychological distress. Participants will be in this research study for 3 months. After screening and onboarding, they will be asked to: * participate in 18 days of the Mindwire program * answer a 45-60 minute online survey immediately before, immediately after, and approximately six weeks after the Mindwire program * participate in a 60-90 minute interview asking about their experience going through the program