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Study identifier: NCT05921201 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Preventing Depression of Chinese American Adolescents by RRE

Condition: Subclinical Depressive Symptoms  ·  Sponsor: Northeastern University

PhaseNA
Planned participants110
Who can joinAll sexes, 14 Years to 18 Years
Healthy volunteersYes

About this study

The goal of this clinical trial is to test if a culturally sensitive mobile health application (Relax, Reflect, Empower-RRE) is feasible and effective in promoting psychological wellbeing and reducing depressive symptoms among Chinese American adolescents (CAA). We will conduct a pilot study of a community sample of 110 CAAs, ages 14-18. We will use adaptive randomization to assign 55 participants to the RRE intervention for 5 days/week for 3 months and 55 to the control group who will receive a wellness check-in text message 5 days/week for 3 months. The main aims/research questions are, 1) To evaluate feasibility and acceptability of RRE. Assessments include both subjective (CAAs' perceptions of feasibility and acceptability of RRE through Mobile Application Rating Scale and open-ended questions) and objective (CAAs' frequency and duration of RRE access automatically recorded) measures. Our hypothesis is that participants in the RRE group will find RRE feasible and acceptable. 2) To investigate CAAs' changes in depressive symptoms, coping self-efficacy, and psychological wellbeing. We will compare if these changes differ in the RRE group and control group. Participants in both RRE and control groups will complete measures of outcomes (depression, coping self-efficacy, psychological wellbeing) and influencing factors (acculturative stress, experiences of discrimination, life events) at three time points: baseline, the end of the preventive intervention (the12th week), and on…

This description comes directly from the study's public registry record.

Talk to the study team

CHIEH LI, EdD  ·  6173734683  ·  c.li@northeastern.edu

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Locations (1)

Northeastern UniversityBoston, Massachusetts, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05921201