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N/A N=168 Randomized Double-blind Health Services Research

Motivational Interviews for Depression in Primary Care

Major Depression

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

OutcomeResultp-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.
View full record on ClinicalTrials.gov →

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.

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