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Acupuncture for Antenatal Depression.

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000250538
Acronym
AcuAnteDep
Enrollment
57
Registered
2015-03-19
Start date
2015-03-05
Completion date
2016-09-30
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Depression in pregnancy is common and also associated with detrimental consequences to both mother and child. Current treatments are limited in that they are not universally effective and also many pregnant women are reluctant to take anti-depressant medications during pregnancy, due to fear of negative foetal effects. Acupuncture may offer a safe alternative as preliminary evidence is suggestive that it is effective in reducing depressive symptoms both during pregnancy and also into the postnatal period. In order to strengthen this evidence base further research is required. How acupuncture may achieve this effect is also unknown and in order to investigate this further, this study aims to assess whether acupuncture positively influences a hormone that is involved in stress buffering, mood stabilisation and maternal / infant bonding.

Interventions

A one hour depression specific individually tailored acupuncture protocol, will be performed every week for eight weeks, from gestation week 24 through to 31 inclusive, by the chief investigator, on randomised consenting depressed pregnant women.

Sponsors

Western Sydney University - National Institute of Complementary Medicine
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Investigator)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

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.

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 2, 2026