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Clinical Trials/NCT01634022
NCT01634022
Completed
Not Applicable

Effectiveness of Acupuncture on Treating Major Depressive Disorder

Massachusetts General Hospital1 site in 1 country64 target enrollmentMay 2005
ConditionsDepression

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Depression
Sponsor
Massachusetts General Hospital
Enrollment
64
Locations
1
Primary Endpoint
Change in scores on the Hamilton Depression Rating Scale, 17 items (HAM-D-17)
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

Acupuncture is a popular complementary/alternative therapy that has been in use for thousands of years for the treatment of various medical and psychiatric conditions, including Major Depressive Disorder (MDD). In this study, the investigators applied the investigators acupuncture-treatment-for-depression protocol, based on Traditional Chinese Medicine (TCM) principles for treating MDD, to depressed patients not taking any antidepressant medications (a protocol that the investigators previously piloted as a medication augmentation therapy for partial responders with MDD).

The investigators specifically investigated the efficacy, safety, and tolerability of this TCM-based protocol for such patients, as well as potential differences in outcomes between weekly vs. twice-weekly treatment. The investigators hypothesized that acupuncture monotherapy would be associated with a response rate of at least 50%, which the investigators defined as a decrease in depressive symptoms from the beginning to the end of the study of 50% or more, and that the response would be greater among patients who received acupuncture 2 times per week (vs. 1 time per week). The investigators also hypothesized that acupuncture would be associated with minimal side effects.

Registry
clinicaltrials.gov
Start Date
May 2005
End Date
November 2011
Last Updated
13 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Albert Yeung

Director of Primary Care Research, Depression Clinical and Research Program

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Has current or past DSM-IV MDD diagnosis based on SCID; AND current 17-Hamilton Rating Scale for Depression (BRSD) score of 14 or above
  • Age between 18-65
  • No treatment with antidepressant(s) in the past 3 months
  • If patient has received psychotherapy, no initiation or termination of therapy in the past 3 months.

Exclusion Criteria

  • Patients with primary diagnosis other than Major Depressive Disorder, or any history of psychosis or mania.
  • Conditions that could make it difficult to conclusively determine that depressive symptoms were the result of MDD and not some other condition, including substance abuse or dependence within the last 6 months, medical conditions that could produce depression, including epilepsy, history of an abnormal EEG, severe head trauma, or stroke.
  • Serious uncontrolled medical conditions \[e.g. poorly controlled diabetes, severe congestive heart failure\], or other medical conditions that have not been stable for at least 3 months.
  • Electroconvulsive therapy (ECT) during the last year.
  • Current active suicidal or self-injurious potential necessitating immediate treatment.
  • Currently receiving concomitant Acupuncture Treatment, or any Acupuncture treatment in the past three months.

Outcomes

Primary Outcomes

Change in scores on the Hamilton Depression Rating Scale, 17 items (HAM-D-17)

Time Frame: Baseline and all acupuncture sessions (weekly) for 8 weeks

The HAM-D-17 is a clinician-rated assessment (structured interview) of patients' depressive symptoms. Questions focus on depressive symptoms during the past 7 days, and higher cumulative scores (possible responses to each item range from 0-4 or 0-2) indicate more severe depression.

Secondary Outcomes

  • Response to treatment, defined as a 50% or greater improvement in HAM-D-17 score compared to baseline(Baseline and all acupuncture sessions (weekly) for 8 weeks)

Study Sites (1)

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