An Interactive Mobile Health (mHealth) App as Intervention for High Anxiety and Depression in College Students

NCT07017569 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 125

Last updated 2025-06-12

No results posted yet for this study

Summary

The goal of this clinical trial is to learn if a mobile health app called mHELP can help college students manage anxiety, stress, and depression.

The main questions it aims to answer are:

* Does using the mHELP app reduce anxiety, stress, and depression symptoms both over time and in real-time?
* Does the app help students engage with mental health services and self-management tools?

Researchers will compare students who use the full version of the mHELP app to those who use a control version with limited features.

Participants will:

* Use an Apple Watch and iPhone app for 10 weeks
* Receive reminders to complete weekly mental health questionnaires
* Tap a button to report high-stress moments or respond to automatic alerts from the app
* Intervention group will use app features like breathing exercises, journaling, and educational videos
* Intervention group will receive 2 free telehealth counseling sessions

Conditions

  • Anxiety
  • Depression - Major Depressive Disorder
  • Stress

Interventions

BEHAVIORAL

Mobile health application

This group will receive the mHELP mobile and watch application with full functionality which provides weekly self-assessment and self-reported events PLUS self-management functionality. The self- management functionality includes additional on-demand features (see the attached list of features). These include * a breath functionality that provides a times breathing exercise similar to the one provided by the Apple iWatch; users can see changes in their heart rate during the breathing exercise and will see a summary of heart rate changes * a calendar features that allows students to upload their class schedule and see different activities such as self-assessments * a journaling feature that allows participants to write a journal * a task list to take note of major tasks and add them to calendar * a set of relaxation media including videos and audios that participants can use on demand

Sponsors & Collaborators

Principal Investigators

  • Farzan Sasangohar, Ph.D. Industrial Engineering · Texas A&M University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-20
Primary Completion
2021-12-15
Completion
2021-12-15

Countries

  • United States

Study Locations

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Entities

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 NCT07017569 on ClinicalTrials.gov