MedPath

Treatment Choices for Improving Adherence and Outcome

Not Applicable
Completed
Conditions
Major Depression
Registration Number
NCT00194948
Lead Sponsor
Weill Medical College of Cornell University
Brief Summary

This study will determine the effectiveness of offering primary care patients their preferred treatment versus one that is less desirable in improving treatment adherence and outcome.

Detailed Description

This study investigates whether offering primary care patients treatment that is congruent with their preferred first choice improves adherence and outcomes, in comparison to offering treatment that is not congruent with their preferred first choice. All subjects are offered a treatment with demonstrated efficacy, namely either the antidepressant medication escitalopram or Interpersonal Psychotherapy for 5 months. We hypothesize that patients who receive congruent treatment will be more likely to initiate treatment, adhere to treatment, and achieve depression remission.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • age 21-99
  • English-speaking
  • DSM-IV criteria for major depression
Exclusion Criteria
  • unable to give informed consent
  • MMSE<24
  • DSM-IV diagnosis of bipolar disorder, psychotic disorder, current alcohol or substance abuse
  • active suicide ideation
  • aphasia
  • acute or severe medical illness
  • currently receiving either antidepressant medication or psychotherapy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
treatment initiation
treatment adherence
Secondary Outcome Measures
NameTimeMethod
depressive symptomatology

Trial Locations

Locations (2)

Weill Medical College of Cornell University

🇺🇸

White Plains, New York, United States

Cornell Internal Medicine Associates

🇺🇸

New York, New York, United States

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