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Clinical Trials/ACTRN12615000250538
ACTRN12615000250538
Completed
未知

A pragmatic randomised controlled trial evaluating acupuncture as an antenatal intervention for the treatment of antenatal depression.

Western Sydney University - National Institute of Complementary Medicine0 sites57 target enrollmentMarch 19, 2015

Overview

Phase
未知
Intervention
Not specified
Conditions
Antenatal Depression
Sponsor
Western Sydney University - National Institute of Complementary Medicine
Enrollment
57
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Antenatal depression is common, with wide-ranging detrimental consequences. Despite this, symptomologies are frequently inadequately managed. Consequently, women seek out alternatives. Preliminary evidence suggests acupuncture may provide a safe and potentially effective adjunct treatment. This study further examined this possibility. In this RCT, fifty-seven women meeting Edinburgh Postnatal Depression Scale (EPDS) scores greater than or equal to 13 were randomised to either individually tailored, depression specific acupuncture, progressive muscle relaxation (PMR) comparator, or treatment as usual. Women were also interviewed regarding their experiences of receiving acupuncture. Focus groups were in addition conducted with midwives to ascertain their views of the study. Findings demonstrated significantly reduced end of the intervention EPDS, stress component of the Depression, Stress and Anxiety scale, and Kessler 6 scores in the acupuncture group, when compared to the PMR and treatment as usual control groups. Mean cortisol: DHEA ratios were in addition significantly increased in the acupuncture group when compared to treatment as usual. Interviews confirmed acupuncture recipients perceived benefits. Midwives also reported receiving positive feedback from participants regarding benefits, as well as observing the improved disposition of recipients. Findings suggest acupuncture reduced or buffered stress, increased coping, and improved psychological well-being.

Registry
who.int
Start Date
March 19, 2015
End Date
April 3, 2017
Last Updated
6 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Western Sydney University - National Institute of Complementary Medicine

Eligibility Criteria

Inclusion Criteria

  • Pregnant women will be eligible if they are: 18 years of age or older, at 24 weeks of gestation, currently experiencing a mood disorder and have a Edinburgh Postnatal Depression Scale (EPDS) scores of greater than or equal to 13\.

Exclusion Criteria

  • Women experiencing: a major depressive episode more than 2 years duration; psychotic or manic features rendering them incapable of consent; post\-traumatic stress disorder and phobia to needles; a current psychiatric assessment of suicidal risk; a condition necessitating bed rest; bleeding disorders and or other major obstetric risks will be excluded; as will those receiving acupuncture or PMR outside of the study.

Outcomes

Primary Outcomes

Not specified

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