Placebo pills (pills with no active ingredients) have been shown in research studies to somehow produce self-healing processes. The purpose of this study is to determine whether people will be willing to enter an open-label non-deceptive placebo treatment for Major Depressive Disorder (MDD) and whether open-label placebo can be effective for treating MDD in the context of a supportive physician-patient relationship.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
20
Participants take open-label placebo pills - two twice daily for four weeks.
Massachusetts General Hospital
Boston, Massachusetts, United States
Feasibility
The primary outcome measure is feasibility, which was operationalized as the number of in-person screens for this study.
Time frame: One year
Pre-Post Efficacy
The magnitude of the pre-post effect across 4 weeks of treatment, as measured by the Hamilton Rating Scale for Depression-17 (HAMD-17). The HAMD-17 measures depression severity, and has a minimum value of 0 and a maximum value of 52 units on a scale, where higher scores indicate more severe depression.
Time frame: Screen and 4 weeks (immediate treatment); Baseline and 4 weeks (waitlist treatment)
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