PERsonalized Mood Augmentation Trial for Depressed Mood (PERMA)

University of California San Diego

Status: Completed

Conditions: Depression

Treatments: Behavioral: Personalized Behavioral Intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT05662254

PERMA

Details and patient eligibility

About

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

Full description

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.

Enrollment: 40 patients

Sex: All

Ages: 15+ years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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40 participants in 1 patient group

Personalized Behavioral Intervention

Experimental group

Description:

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

Treatment:

Behavioral: Personalized Behavioral Intervention