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Evaluating The Impact of A Mental Health App on Depression and Resilience Among Medical Students

NCT07397299 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 220

Last updated 2026-02-13

No results posted yet for this study

Summary

This randomized controlled trial aims to determine whether access to a mental health app improves resilience and reduces depressive symptoms among medical students over a three-month period.

Compared to the control group, researchers hypothesized that medical students in the intervention group are expected to show:

* Significant reductions in depressive symptoms and greater improvements in resilience after three months of usage.
* Significant reduction in thoughts of self-harm and anxiety, and improvement in self-esteem after three months of usage.

Researchers will compare two groups to evaluate the app's impact on wellbeing:

* Intervention group: Receives immediate full access to the mental health app.
* Control group: Receives basic, without full access to the mental health app.

Participants will explore and experience the various features offered in the mental health app over a three-month period.

Conditions

  • Depression - Major Depressive Disorder
  • Resilience

Interventions

BEHAVIORAL

Full digital mental health intervention

Name of the mental health app - Intellect: Create A Better You

BEHAVIORAL

Basic digital mental health intervention

Name of mental health app - Intellect: Create a Better You

Sponsors & Collaborators

  • National University of Malaysia

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
30 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-02-11
Primary Completion
2026-06-30
Completion
2026-06-30

Countries

  • Malaysia

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07397299 on ClinicalTrials.gov