Mobile Self-Management Program for Stress Reduction in Young Adults
2 other identifiers
interventional
211
1 country
1
Brief Summary
The goal of this clinical trial is to learn if a mobile self-management program that combines Positive Psychology (PP) and Behavioral Activation (BA) helps reduce stress in young adults in South Korea. It will also examine how the program affects depression, anxiety, and resilience. The main questions it aims to answer are: Does the program lower stress levels in young adults with high stress? Does the program improve other aspects of mental health, such as depression, anxiety, and resilience? Researchers will compare the mobile program to a wait-list control group to see if the program works to improve stress management. Participants will: Be randomly assigned to either the program group or a wait-list control group Use the mobile program for 4 weeks with guided activities, followed by 4 weeks of self-directed use Complete surveys at the start, week 2, week 4, and week 8 about their stress, depression, anxiety, and resilience
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2023
Typical duration for not_applicable
1 active site
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
September 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 30, 2025
CompletedFirst Submitted
Initial submission to the registry
September 11, 2025
CompletedFirst Posted
Study publicly available on registry
September 16, 2025
CompletedResults Posted
Study results publicly available
January 8, 2026
CompletedJanuary 8, 2026
December 1, 2025
1.3 years
September 11, 2025
September 15, 2025
December 17, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Stress at Week 8
Stress was measured using the Korean version of the Perceived Stress Scale - 10 items (PSS-10). The total score ranges from 0 to 40, with higher scores indicating greater perceived stress. Although the scale does not provide a standardized cut-off, prior studies have used a score of 14 or higher to define moderate-to-high levels of stress, and this threshold was applied in the present study.
Week 8
Secondary Outcomes (15)
Stress at Baseline
Baseline
Stress at Week 2
Week 2
Stress at Week 4
Week 4
Depression (PHQ-9) at Baseline
Baseline
Depression (PHQ-9) at Week 2
Week 2
- +10 more secondary outcomes
Study Arms (2)
Intervention group
EXPERIMENTALParticipants receive a mobile self-management intervention that integrates Positive Psychology and Behavioral Activation. The program includes 4 weeks of guided sessions followed by 4 weeks of self-directed use.
Wait-list Control
NO INTERVENTIONParticipants do not receive the intervention during the first 8 weeks but are offered access to the program after the study period.
Interventions
The mobile self-management program consisted of a 4-week guided intervention phase followed by a 4-week self-directed period to encourage continued use. The guided phase was organized around weekly objectives: (1) experiencing positive affect, (2) identifying personal strengths, (3) applying strengths in daily life, and (4) planning a positive future. Program activities included emotional check-ins, gratitude journaling, mindfulness practice, positive behavioral tasks, and goal setting. During the self-directed phase (Weeks 5-8), participants selected from 10 recommended activities tailored to their strengths, promoting sustained engagement and self-management. The program integrated Positive Psychology and Behavioral Activation strategies to reduce stress, enhance resilience, and foster positive behavioral change.
Eligibility Criteria
You may qualify if:
- Age 19-34 years at the time of participation
- Proficiency in using digital devices
- Use of an Android-based smartphone or tablet
- Score of ≥14 on the Perceived Stress Scale-10 (PSS-10)
- Provision of informed consent for random assignment
You may not qualify if:
- Score \<14 on the Perceived Stress Scale-10 (PSS-10)
- Declines random assignment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
College of Nursing, The Catholic University of Korea
Seoul, Seoul, 06591, South Korea
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Limitations and Caveats
A key limitation of this study was participant attrition during the 8-week intervention period, as some participants did not complete all weekly or follow-up surveys. This loss to follow-up may have limited the ability to fully determine the intervention's effect over time and reduced the precision of longitudinal comparisons between groups.
Results Point of Contact
- Title
- Hyunjoo Na, Associate professor, PI
- Organization
- College of Nursing, The Catholic University of Korea
Publication Agreements
- PI is Sponsor Employee
- No
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate professor
Study Record Dates
First Submitted
September 11, 2025
First Posted
September 16, 2025
Study Start
September 1, 2023
Primary Completion
December 31, 2024
Study Completion
August 30, 2025
Last Updated
January 8, 2026
Results First Posted
January 8, 2026
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share
The study's informed consent form restricts use of data to this research only. Therefore, IPD will not be shared with other researchers.