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Acupuncture as a Supplemental Treatment for Bipolar Depression

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00071669
First Posted: October 30, 2003
Last Update Posted: April 15, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
National Institute of Mental Health (NIMH)
Information provided by:
University of Texas Southwestern Medical Center
  Purpose
The purpose of this study is to evaluate the effectiveness of acupuncture in the treatment of Bipolar Depression.

Condition Intervention Phase
Bipolar Disorder Procedure: Acupuncture Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single
Primary Purpose: Treatment
Official Title: Adjunctive Acupuncture as a Treatment for Bipolar Depression

Resource links provided by NLM:


Further study details as provided by University of Texas Southwestern Medical Center:

Estimated Enrollment: 30
Study Start Date: November 2001
Detailed Description:
Patients receive 8 weeks (12 sessions) of acupuncture treatment plus stable medication. Patients are randomly assigned to receive either acupuncture designed to relieve symptoms of depression or acupuncture designed to relieve some other legitimate physical condition. A comparison group of patients who take medication but do not receive acupuncture is assessed to evaluate the effectiveness of medication alone. Patients participate in clinical assessment each week, which includes visiting with a psychiatrist and completing symptom rating scales.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Meet DSM-IV criteria for bipolar I disorder or bipolar II disorder
  • Demonstrate symptoms of depression as determined by a minimum score of 25 on the Inventory for Depressive Symptoms-Clinician Rated Scale
  • Have taken stable psychoactive medications for at least 30 days prior to study entry
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00071669


Locations
United States, Texas
Bipolar Disorder Clinic and Research Program
Dallas, Texas, United States, 75390
Sponsors and Collaborators
University of Texas Southwestern Medical Center
National Institute of Mental Health (NIMH)
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
ClinicalTrials.gov Identifier: NCT00071669     History of Changes
Other Study ID Numbers: R03MH061589 ( U.S. NIH Grant/Contract )
DSIR AT-SO
First Submitted: October 29, 2003
First Posted: October 30, 2003
Last Update Posted: April 15, 2013
Last Verified: November 2005

Keywords provided by University of Texas Southwestern Medical Center:
Mood Disorder
Acupuncture

Additional relevant MeSH terms:
Depression
Bipolar Disorder
Behavioral Symptoms
Bipolar and Related Disorders
Mental Disorders