N/A
N=168
Motivational Interviews for Depression in Primary Care
Major Depression
Bottom Line
View on ClinicalTrials.gov: NCT01114334 ↗Enrolled (actual)
168
Serious AEs
0.0%
Results posted
Apr 2017
Primary outcome: Primary: Depression Remission — 4; 15 participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Guideline-Based Medical Management (Behavioral); Motivational Interviewing for Depression (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Denver Health and Hospital Authority
- Primary completion
- Dec 2012
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Depression Remission |
4; 15 | — |
| SECONDARY Adherence to Treatment With Antidepressant Medication |
11; 15 | — |
| SECONDARY Patient Health Questionnaire-9 Instrument for Assessing Depressive Symptoms |
11.66; 9.16 | — |
Summary
The purpose of the study is to determine whether motivational interviewing with guideline-based medical management for depression will significantly improve time to depression recovery and increase the proportion of subjects in recovery compared to guideline-based medical management alone over 9 months.
Eligibility Criteria
Inclusion Criteria
- Women and men aged 18 or older presenting at one of the seven DHH study clinics with a new treatment episode for depression will be considered for the study.
- The PHQ-9 is used to define depression category with a sensitivity and specificity for MDD of at least 88%. Patients must have PHQ-9≥10 to ensure sufficient severity to warrant intervention.
- A new treatment episode is defined as no treatment with an antidepressant medication for emotional problems over the previous 90 days, nor evidence-based psychotherapy for depression.
- The subjects must have major depression as determined by diagnostic schedule.
Exclusion Criteria
- Receipt of an antidepressant medication in the previous 90 days other than a low-dose TCA for pain or Trazodone for sleep (e.g. amitriptyline ≤ 50 mg a day or Trazodone ≤ 100 mg at night).
- Current interpersonal or cognitive behavioral psychotherapy that focuses on depression.
- Female subjects who are either pregnant or nursing.
- Subjects with drug or alcohol dependency or abuse (except for nicotine or caffeine) within the preceding 6 months.
- High risk for suicide.
- Inability to communicate in English.
- No personal telephone or homeless.
- Lifetime bipolar disorder.
- Psychosis.
- Subjects with a lifetime history of autism, mental retardation, or pervasive developmental disorders.
- Subjects with uncorrected hypothyroidism or hyperthyroidism.
- Serious, unstable illnesses including hepatic, renal, gastroenterologic, respiratory, cardiovascular (including ischemic heart disease), endocrinologic, neurologic, immunologic, or hematologic disease.
Data sourced from ClinicalTrials.gov (NCT01114334). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.