Text Messaging and Cognitive Behavioral Therapy for Depression

Not Applicable

Completed

• Conditions: Depression
• Interventions: Behavioral: Group CBT for Depression with MoodText; Behavioral: Group CBT for Depression

• Registration Number: NCT01083628
• Lead Sponsor: University of California, San Francisco

Brief Summary

This study aims to asses whether adding automated text messaging to group cognitive behavioral therapy for depression increases engagement which may lead to improved outcomes.

Detailed Description

Background: Cognitive Behavioral Therapy (CBT) for depression is efficacious, but effectiveness is limited when implemented in low-income settings due to engagement difficulties including nonadherence with skill-building homework and early discontinuation of treatment. Automated messaging can be used in clinical settings to increase dosage of depression treatment and encourage sustained engagement with psychotherapy.

Objectives: The aim of this study was to test whether a text messaging adjunct (mood monitoring text messages, treatment-related text messages, and a clinician dashboard to display patient data) increases engagement and improves clinical outcomes in a group CBT treatment for depression. Specifically, the investigators aim to assess whether the text messaging adjunct led to an increase in group therapy sessions attended, an increase in duration of therapy attended, and reductions in Patient Health Questionnaire-9 item (PHQ-9) symptoms compared with the control condition of standard group CBT in a sample of low-income Spanish speaking Latino patients.

Methods: Patients in an outpatient behavioral health clinic were assigned to standard group CBT for depression (control condition; n=40) or the same treatment with the addition of a text messaging adjunct (n=45). The adjunct consisted of a daily mood monitoring message, a daily message reiterating the theme of that week's content, and medication and appointment reminders. Mood data and qualitative responses were sent to a Web-based platform (HealthySMS) for review by the therapist and displayed in session as a tool for teaching CBT skills.

Study Timeline

• Study First Submitted: 2010-02-19
• Study First Submitted QC: 2010-03-08
• Study First Posted: 2010-03-10
• Study Start: 2014-01
• Primary Completion: 2016-09
• Study Completion: 2017-04
• Results First Submitted: 2018-12-21
• Status Verified: 2019-07
• Results First Submitted QC: 2019-07-02
• Last Update Submitted: 2019-07-02
• Results First Posted: 2019-08-12
• Last Update Posted: 2019-08-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 85

Inclusion Criteria

• Participation in CBT group at San Francisco General Hospital

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Exclusion Criteria

• Active suicidality
• Active and severe psychosis

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group CBT for Depression with MoodText'	Group CBT for Depression with MoodText	Group cognitive behavioral therapy utilizing the BRIGHT manual for depression along with automated text messaging for mood monitoring and reminder of session content
Group CBT for Depression	Group CBT for Depression	Standard group cognitive behavioral therapy utilizing the BRIGHT manual for depression

Primary Outcome Measures

Name	Time	Method
PHQ-9 Depression Symptoms	16 weeks	The PHQ-9 (Patient Health Questionnaire - 9) is commonly used to screen for depression and to monitor progression of depressive symptoms over time. The scores represent the following depression severity: 0-4: minimal depression, 5-9: mild depression, 10-14: moderate depression, 15-19: moderately severe, 20-27: severe. A score of 10 is often recommended as the cut-off score for diagnosing an episode of depression that may require treatment.

Secondary Outcome Measures

Name	Time	Method
Attendance	16 weeks	Number of sessions attended
Duration of Therapy Attended	16 weeks	Number of weeks until patients dropped out of therapy

Trial Locations

Locations (1)

San Francisco General Hospital; 🇺🇸 San Francisco, California, United States