Motivational Interviewing to Reduce Substance Use Among Depression Patients
1 other identifier
interventional
307
1 country
1
Brief Summary
The study aims to evaluate the effectiveness of an intervention to reduce alcohol and drug use and depression symptoms, improve functional status and promote appropriate health services utilization, in a sample of 300 adults seeking treatment for depression who also report hazardous drinking or drug use with depression.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable depression
Started Oct 2010
Longer than P75 for not_applicable depression
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2014
CompletedFirst Submitted
Initial submission to the registry
April 7, 2015
CompletedFirst Posted
Study publicly available on registry
April 20, 2015
CompletedJune 10, 2015
June 1, 2015
3.8 years
April 7, 2015
June 8, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Hazardous drinking in the prior 30 days (Self-reported number of days of hazardous drinking)
Self-reported number of days of hazardous drinking (3+ drinks per day for women / 4+ drinks per day for men) in the prior 30 days.
6 months
Drug use in the prior 30 days (Self-reported number of days of drug use)
Self-reported number of days of drug use (illegal drug use or misuse of prescription drugs) in the 30 prior days.
6 months
Hazardous drinking in the prior 30 days (Self-reported number of days of hazardous drinking)
Self-reported number of days of hazardous drinking (3+ drinks per day for women / 4+ drinks per day for men) in the prior 30 days. We examine the change between use at 6 months and use at 12 months to measure long term intervention impact.
12 months
Drug use in the prior 30 days (Self-reported number of days of drug use)
Self-reported number of days of drug use (illegal drug use or misuse of prescription drugs) in the 30 prior days. We examine the change in use between 6 months and 12 months to measure long term intervention impact.
12 months
Secondary Outcomes (2)
Depression symptoms (Patient health questionnaire (PHQ-9) score)
12 months
Adequate mental health treatment (Number of participants receiving 12 weeks' continuous treatment at the Kaiser Permanente Outpatient Psychiatry Department)
3 months
Study Arms (2)
Motivational Interviewing
EXPERIMENTALThe motivational interviewing (MI) intervention consisted of one 45-minute in-person MI session followed by two 15-minute telephone "booster" sessions
Control
ACTIVE COMPARATORParticipants received a brochure on alcohol and drug use risks.
Interventions
* One in-person motivational interviewing session intervention that lasts for 45-minutes * Additional two 15-minute telephone "booster" sessions post in-person 45 minute sessions
Eligibility Criteria
You may qualify if:
- Hazardous drinking (i.e., ≥ 3 drinks in a day for women and ≥ 4 drinks in a day for men)
- Drug use (including any illicit drug use and non-prescribed use of prescription drugs in the prior 30 days)
- Moderate or greater symptoms of depression based on a score of ≥ 5 on the Patient Health Questionnaire (PHQ-9)
You may not qualify if:
- Current mania or psychosis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Kaiser Permanente Medical Center Southern Alameda County
Union City, California, 94545, United States
Related Publications (245)
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PMID: 18373724BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Derek D Satre, PhD
University of California, San Francisco
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 7, 2015
First Posted
April 20, 2015
Study Start
October 1, 2010
Primary Completion
August 1, 2014
Study Completion
August 1, 2014
Last Updated
June 10, 2015
Record last verified: 2015-06