NCT07379541

Brief Summary

As the primary users of smartphones, emerging adults represent a key population for such research. Using a randomised controlled trial, the investigators compared mindfulness-of-death meditation with traditional mindfulness meditation to evaluate the unique effects of the former on problematic smartphone use. The investigators also examined potential psychological pathways-namely increases in self-esteem and meaning in life, and reductions in perceived stress-through which the intervention may exert its benefits.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
259

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Feb 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 23, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 25, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 25, 2025

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

January 23, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

January 30, 2026

Completed
Last Updated

February 23, 2026

Status Verified

January 1, 2026

Enrollment Period

2 months

First QC Date

January 23, 2026

Last Update Submit

February 20, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Smartphone Addiction Scale

    Participants' problematic smartphone use was assessed using the 33-item Smartphone Addiction Scale (SAS) \[Kwon et al., 2013\]. Although the original scale employed a 6-point response format, the present study utilized a 5-point Likert scale ranging from 1 (almost never) to 5 (almost always; α = .88). The scale comprises six dimensions: daily disturbance, positive anticipation, withdrawal symptoms, online intimacy, excessive use, and tolerance. Higher total scores indicate greater severity of problematic smartphone use.

    Baseline, post-intervention (Day 16), and one-month follow-up

Secondary Outcomes (6)

  • Perceived Stress Scale-10

    Baseline, post-intervention (Day 16), and one-month follow-up

  • Philadelphia Mindfulness Scale

    Baseline, post-intervention (Day 16), and one-month follow-up

  • Self-Control Scale for College Students

    Baseline, post-intervention (Day 16), and one-month follow-up

  • Boredom Proneness Scale-Short Form

    Baseline, post-intervention (Day 16), and one-month follow-up

  • Three-Dimensional Meaning in Life Scale

    Baseline, post-intervention (Day 16), and one-month follow-up

  • +1 more secondary outcomes

Study Arms (3)

Mindfulness-Meditation Intervention Group

EXPERIMENTAL

A 16-day mindfulness-based curriculum was implemented as the intervention, with participants completing one 20-min session daily via the online platform.

Behavioral: Mindful Breathing Practice (MBP) - 16-Day Online Meditation Course

Mindfulness-of-Death Group

EXPERIMENTAL

A 16-day mindfulness-of-death curriculum was implemented as the intervention, with participants completing one 20 min online session daily.

Behavioral: Mindfulness of Death (MoD) - 16-Day Online Meditation Course

Wait-list Control Group

NO INTERVENTION

Wait-list Control Group

Interventions

The Mindful Breathing Practice (MBP) intervention is a 16-day online meditation program designed to cultivate present-moment awareness by intentionally anchoring attention on the natural rhythm of breathing. The course consists of 16 daily sessions (approximately 15 minutes each), including brief instructional guidance and guided mindful breathing exercises. Participants are guided to observe the bodily sensations of inhalation and exhalation (e.g., the airflow at the nostrils or the rise and fall of the abdomen) and, when attention wanders, to gently bring it back to the breath with a non-judgmental and accepting attitude. The intervention adopts a non-religious approach, involves no spiritual or religious content, and is suitable for the general population.

Mindfulness-Meditation Intervention Group

The Mindfulness of Death (MoD) intervention is a 16-day online meditation program designed to cultivate awareness of death. The course consists of 16 daily sessions (approximately 20 minutes each), including brief psychoeducational content and guided meditation practice. The initial sessions focus on breathing-based mindfulness to establish attentional stability, followed by mindfulness of death practices that emphasize the inevitability and uncertainty of death while encouraging attention to life and the present moment. The intervention adopts a non-religious approach and does not require participants to hold any religious or spiritual beliefs.

Mindfulness-of-Death Group

Eligibility Criteria

Age18 Years - 29 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • reported no current or past psychiatric diagnosis,
  • exhibited problematic smartphone use,
  • and had a mean daily screen-on time exceeding four hours.

You may not qualify if:

  • aged \<18 or ≥30 years;
  • any current or past psychiatric diagnosis;
  • self-reported absence of problematic smartphone use;
  • mean daily smartphone use ≤4 hours;
  • currently enrolled in any meditation-based intervention;
  • use of psychoactive medication or concurrent psychological treatment;
  • participation in another psychological intervention trial.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Beijing Normal University

Beijing, China

Location

MeSH Terms

Conditions

Internet Addiction Disorder

Condition Hierarchy (Ancestors)

Technology AddictionBehavior, AddictiveCompulsive BehaviorImpulsive BehaviorBehavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Co-Investigator

Study Record Dates

First Submitted

January 23, 2026

First Posted

January 30, 2026

Study Start

February 23, 2025

Primary Completion

April 25, 2025

Study Completion

April 25, 2025

Last Updated

February 23, 2026

Record last verified: 2026-01

Locations