Development and Evaluation of an e-Mental Health Program for Depressive Symptoms
A Digital Approach to Depression: Development and Evaluation of an Electronic Mental Health Program for Depressive Symptoms
1 other identifier
interventional
70
1 country
1
Brief Summary
This randomized controlled trial evaluates the effectiveness of an electronic mental health program (e-MHP) in reducing depressive symptoms among adults. The study also compares outcomes between clinical and nonclinical populations.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2023
Shorter than P25 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
May 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 31, 2024
CompletedFirst Submitted
Initial submission to the registry
August 17, 2025
CompletedFirst Posted
Study publicly available on registry
April 22, 2026
CompletedApril 22, 2026
April 1, 2026
9 months
August 17, 2025
April 18, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Depression Severity
Depression severity will be assessed using a standardized depression scale. Scores will be analyzed as continuous variables. Unit of Measure: Scale score (e.g., 0-27) Interpretation: \<5 = normal 5-9 = mild 10-14 = moderate 15-19 = moderately severe ≥20 = severe
From enrollment to the end of intervention at 12 weeks. Post-test is held at 12 weeks after the intervention.
Other Outcomes (3)
Change in Anhedonia
From enrollment to the end of intervention at 12 weeks. Post-test is held at 12 weeks after the intervention.
Change in Self-Esteem
From enrollment to the end of intervention at 12 weeks. Post-test is held at 12 weeks after the intervention.
Effectiveness analysis of a digital mental health program intervention on positive and negative suicide ideation.
From enrollment to the end of intervention at 12 weeks. Post-test is held at 12 weeks after the intervention.
Study Arms (2)
Digital mental health program group
EXPERIMENTALA 12-week digital mental health program with nine interactive online modules addressing depression literacy, cognitive reframing, emotional acceptance, behavioral activation, interpersonal skills, relaxation, healthy lifestyle, and positive psychology. Modules (\~30 min each) were self-paced, with interactive exercises to reinforce skill use.
control group
NO INTERVENTIONParticipants did not receive the digital mental health program and continued their usual daily routines without additional intervention.
Interventions
The digital mental health program comprises nine interactive online modules that target knowledge of depression, cognitive reframing, emotional acceptance, behavioral activation, interpersonal skills, relaxation, a healthy lifestyle, and positive psychology.
Eligibility Criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Chang Hsiu-Julead
- National Science and Technology Council, Taiwancollaborator
Study Sites (1)
National Yang Ming Chiao Tung University
Taipei, Taiwan, 155, Taiwan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
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
- SPONSOR INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
August 17, 2025
First Posted
April 22, 2026
Study Start
May 1, 2023
Primary Completion
January 31, 2024
Study Completion
January 31, 2024
Last Updated
April 22, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share
We do not plan to share IPD due to privacy concerns, legal restrictions, institutional policies, or no consent from participants. Our ethics approval or consent form does not allow sharing.