Clinical Trials Directory

Trials / Completed

CompletedNCT01178008

Pilot Study on the Use of Acupuncture for Postpartum Depression

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
The University of Hong Kong · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The proposed study is a randomized controlled trial to examine the efficacy and safety of active acupuncture versus placebo acupuncture for the treatment of postpartum depression. The investigators hypothesis is that active acupuncture would be superior to placebo acupuncture in the short-term treatment of postpartum depression.

Detailed description

This study will be a randomized, controlled, subject- and assessor-blind trial in patients with postpartum depression. Eligible subjects will be randomly assigned to active acupuncture or placebo acupuncture. The subjects will receive acupuncture treatment twice per week for 4 consecutive weeks. The acupuncturist of this trial will not participate in data collection and data entry. The trial assessor will be blind to the subjects' treatment allocation.

Conditions

Interventions

TypeNameDescription
PROCEDUREActive acupunctureActive acupuncture regimen consists of electroacupuncture stimulation on cranial and body acupoints which are empirical for treating depression in term of traditional Chinese medicine theory. It is done by a registered Chinese medicine practitioner with at least 3 years experience of providing acupuncture treatment. An electric-stimulator is connected to these needles to give an electric-stimulation in a continuous wave The needles will be left for 30 min and then removed. Acupuncture treatment will consist of two sessions per week for 4 consecutive weeks.
PROCEDUREPlacebo acupunctureStreitberger's non-invasive acupuncture needles will be applied to serve as placebo control at the same acupoints and the same stimulation modality, except that the needles only affixed on the skin with adhesive tapes instead of insertion. Since all the points used are beyond patients' vision as they lay on bed, they could not visualize the acupuncture procedure. The acupuncturist, setting, treatment frequency, and duration of the treatment course are the same as the active acupuncture group.

Timeline

Start date
2010-05-01
Primary completion
2011-12-01
Completion
2012-06-01
First posted
2010-08-09
Last updated
2013-01-16

Locations

3 sites across 1 country: Hong Kong

Source: ClinicalTrials.gov record NCT01178008. Inclusion in this directory is not an endorsement.