PERsonalized Mood Augmentation Trial for Depressed Mood

University of California, San Diego40 enrolled

Overview

The goal of this open-label single-arm study is to test personalized behavioral intervention for depressed mood.

The goal of this open-label single-arm study is to test personalized behavioral intervention for depressed mood. After an initial period (2-4 weeks) of mood and lifestyle monitoring using smartphone and smartwatch data, participants will be assigned to an evidenced-based behavioral plan that target their lifestyle for 6 weeks. The trial will evaluate changes in depressed mood, associated health behaviors and cognition.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Depression

Interventions

Personalized Behavioral InterventionBEHAVIORAL

Behavioral lifestyle intervention assigned according to each participant's mood and lifestyle data patterns.

Eligibility

Sex: ALLMin age: 15 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Mild to moderate depression per PHQ9 symptom ratings Exclusion Criteria: * active substance abuse/dependence * psychotic disorders * bipolar disorder * eating disorder * displaying acutely suicidal behaviors

Locations (1)

UC San Diego Health Psychiatry

San Diego, California, United States

Outcomes

Primary Outcomes

PHQ9

Depression Symptoms on the Patient Health Questionnaire 9-item (PHQ9) scale, min 0 max 27 with lower scores representing better outcome

Time frame: 12 weeks

Data from ClinicalTrials.gov

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