Effectiveness of a digital mindfulness-based program on the mental health of college students: A randomized controlled trial in China

Last registered on September 28, 2026

Pre-Trial

Trial Information

General Information

Title
Effectiveness of a digital mindfulness-based program on the mental health of college students: A randomized controlled trial in China
RCT ID
AEARCTR-0019716
Initial registration date
September 24, 2026

Initial registration date is when the trial was registered.

It corresponds to when the registration was submitted to the Registry to be reviewed for publication.

First published
September 28, 2026, 9:45 AM EDT

First published corresponds to when the trial was first made public on the Registry after being reviewed.

Locations

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Primary Investigator

Affiliation
Stanford

Other Primary Investigator(s)

PI Affiliation
Stanford University
PI Affiliation
Stanford University
PI Affiliation
Stanford University
PI Affiliation
Fudan University
PI Affiliation
Stanford University

Additional Trial Information

Status
In development
Start date
2026-09-27
End date
2030-12-31
Secondary IDs
ISRCTN34437131
Prior work
This trial does not extend or rely on any prior RCTs.
Abstract
Mindfulness-based programs (MBPs), rooted in contemplative practices, have emerged as promising interventions for promoting psychological well-being and positive functioning. Increasingly, MBPs are being delivered via digital platforms (i.e., mobile apps) to expand reach (Mrazek et al., 2019). However, no large-scale study has evaluated the effectiveness of a digitally delivered, weekly module-based MBP with pre-recorded guided mindfulness practices for university students in China, a population with a high prevalence of mental health challenges. Building off an evaluation study of an in-person MBP implemented in fall 2025, this study aims to evaluate the impact of a digital MBP specifically tailored for university students. We will investigate the effects on the primary outcomes of anxiety symptoms, depression symptoms, and perceived stress, alongside potential mediators (state mindfulness, emotion regulation skills, self-compassion, gratitude), and secondary well-being indicators (including sleep quality and perceived online social support). The study design will be a two-arm randomized controlled trial (RCT) with undergraduate students enrolled at three universities in China.
External Link(s)

Registration Citation

Citation
Abbey, Cody et al. 2026. "Effectiveness of a digital mindfulness-based program on the mental health of college students: A randomized controlled trial in China." AEA RCT Registry. September 28. https://doi.org/10.1257/rct.19716-1.0
Experimental Details

Interventions

Intervention(s)
Students in the treatment group will receive free access to a sub-application, which they can access directly through the popular social media platform WeChat without needing to separately download. The sub-application will contain brief audio recordings of mindfulness-related content aligned with the eight-week MBP curriculum (the Mindfulness4College Program, implemented in fall of 2025), guided meditation practices, and worksheets to facilitate their completion of brief exercises related to the material. Students will learn core mindful awareness practices such as sitting meditation, body scans, and mindful movement. For the duration of the eight weeks, will be asked to conduct at least 15-20 minutes of mindfulness practice, six days per week.
Intervention Start Date
2026-10-05
Intervention End Date
2026-12-07

Primary Outcomes

Primary Outcomes (end points)

Anxiety symptoms measured using the GAD-7 (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up, weekly during intervention)

Depression symptoms measured using the PHQ-9 (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up, biweekly during intervention)

Perceived stress measured using the Perceived Stress Scale (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up, biweekly during intervention)
Primary Outcomes (explanation)

Secondary Outcomes

Secondary Outcomes (end points)
Emotion regulation measured using the Emotion Regulation Questionnaire (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up, biweekly during intervention)

Trait mindfulness measured using the Five Facet Mindfulness Questionnaire–Short Form (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

Loneliness measured using the UCLA Loneliness Scale (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

Sleep quality measured using the Pittsburgh Sleep Quality Index (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up) and a two-item version of the Pittsburgh Sleep Quality Index (biweekly during intervention)

Flourishing measured using the Flourishing Scale (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

Life satisfaction measured using the Satisfaction with Life Scale (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

Academic performance measured using previous-semester GPA and/or Gaokao score (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

Lifestyle behaviors measured using self-report items assessing the amount and frequency of behaviors, such as screen use and exercise (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

Face-saving attitudes measured using the Face Saving Scale (CPAI-2) (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

Somatic symptoms measured using the Somatic Symptom Scale (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

Acceptability measured using self-report items assessing perceived benefits and adverse effects, as well as qualitative follow-up interviews (post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

Self-compassion measured using the Self-Compassion Scale–Short Form (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, biweekly during intervention)

Experiential avoidance measured using the Brief Experiential Avoidance Questionnaire (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

Gratitude measured using the Gratitude Questionnaire (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up, biweekly during intervention)

Stress mindset measured using the Stress Mindset Scale (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

Online social support measured using the Online Social Support Scale (OSSS) (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

Smartphone addiction measured using the Smartphone Addiction Scale (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

Mental health literacy measured using the MHLq-SVa (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up)

State mindfulness measured using the Multidimensional State Mindfulness Questionnaire (pre-intervention, post-intervention, 3-month follow-up, 6-month follow-up, post-graduation follow-up, biweekly during intervention)









during the intervention
2. Trait mindfulness measured using Five Facet Mindfulness Questionnaire - Short Form at preintervention,
post-intervention, 3-month follow-up, 6-month follow-up, post-graduation followup
3. Loneliness measured using UCLA Loneliness Scale at pre-intervention, post-intervention, 3-
month follow-up, 6-month follow-up, post-graduation follow-up
4. Sleep quality measured using Pittsburgh Sleep Quality Index at pre-intervention, postintervention,
3-month follow-up, 6-month follow-up, post-graduation follow-up, biweekly during
the intervention (two-item version)
5. Flourishing measured using Flourishing Scale at pre-intervention, post-intervention, 3-month
follow-up, 6-month follow-up, post-graduation follow-up
6. Life satisifaction measured using Satisfaction with Life Scale at pre-intervention, postintervention,
3-month follow-up, 6-month follow-up, post-graduation follow-up
Secondary Outcomes (explanation)

Experimental Design

Experimental Design
The experimental design will be a randomized study with undergraduate students recruited
from three universities in China. Using the RCT method of impact evaluation, we will be able to
ensure that the intervention and control groups have similar characteristics at baseline, which is
vital for drawing a causal connection between the intervention and any changes in student. By assuring the similarity of characteristics (such as sex, baseline mental health, etc.) between the treatment and control groups at baseline, we can confidently attribute any
significant differences in outcomes between the control and intervention group to the program. All study participants will receive adequate financial compensation for participating in the study.
Experimental Design Details
Not available
Randomization Method
Randomization will be done using a digital random number generator on a computer
Randomization Unit
Individual
Was the treatment clustered?
No

Experiment Characteristics

Sample size: planned number of clusters
N/A
Sample size: planned number of observations
250
Sample size (or number of clusters) by treatment arms
125 control group, 125 mindfulness group
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
0.4 SD
IRB

Institutional Review Boards (IRBs)

IRB Name
Stanford University Institutional Review Board
IRB Approval Date
2026-09-15
IRB Approval Number
88169
Analysis Plan

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