Developing New Clinical Management Strategies

Completed · Phase 4 · Has a placebo group

Conditions studied: Major Depressive Disorder

In brief

The goal of this study is to develop new methods of administering antidepressant medications that will result in improved drug/placebo separation in randomized controlled trials (RCTs) for Major Depressive Disorder (MDD) and enhanced medication response in open clinical treatment. The highly intensive, weekly visit schedule followed in most antidepressant RCTs radically differs from how antidepressant medications are prescribed in standard clinical practice and is believed to be a major reason why the majority of studies submitted to the Food and Drug Administration (FDA) fail to show a significant difference between medication and placebo. Moreover, a "one size fits all" approach to psychopharmacologic management (i.e., weekly visits for all patients) does not take into account differences between patients that may predispose some individuals to respond positively to frequent follow-up visits, while others may respond negatively or not at all. Clinic visits comprise multiple components that may be therapeutic for depression, including activating patients' behavior, exposing them to medical procedures, permitting social interactions with research staff, and providing supportive meetings with clinicians. Two independent meta-analyses have associated more frequent study visits with increased antidepressant and placebo response as well as decreased separation between medication and placebo. Despite the high costs and potential disadvantages of weekly follow-up visits for patients receiving antidepressant medication, this clinical management strategy has not been studied prospectively to date. It is unknown whether weekly follow-up visits are needed to ensure treatment compliance and patient safety in clinical trials and to what degree contacts with clinicians influence medication and placebo response.

Key facts

Study ID: NCT02082392
Run by: New York State Psychiatric Institute
People needed: 3
Starts: 2012-09-01
Expected to finish: 2015-08-04
Last updated by the study team: 2020-03-03

Who can join

Age: 18 and older, up to 60. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

1. men and women aged 18-60 years
2. diagnosis with Diagnostic and Statistical Manual (DSM) IV Major Depressive Disorder (MDD)
3. 24-item Hamilton Rating Scale for Depression (HRSD) score greater than or equal to 18
4. capable of providing informed consent and complying with study procedures
5. using appropriate contraceptive method if woman of child-bearing age

You may not qualify if…

1. Current comorbid Axis I DSM IV disorder other than Nicotine Dependence, Adjustment Disorder, or Anxiety Disorder
2. diagnosis of substance abuse or dependence (excluding Nicotine Dependence) within the past 12 months
3. present or past history of psychosis, psychotic disorder, mania, or bipolar disorder
4. baseline HRSD score > 28 or HRSD suicide item > 2
5. history of allergic or adverse reaction to escitalopram, or non-response to adequate trial of escitalopram (at least 4 weeks at dose of 20mg) during the current episode
6. current treatment with psychotherapy, antidepressants, antipsychotics, or mood stabilizers
7. CGI-Severity score of 7 at baseline
8. acute, severe, or unstable medical illness

Where it is running

New York State Psychiatric Institute — New York, New York, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.