ACTRN12617000354381
Completed
未知
An investigation examining the efficacy and safety of a multi-nutrient intervention on symptoms of antenatal depression and anxiety in pregnant women who are symptomatic: A double blind, randomized, controlled trial
Professor Julia Rucklidge0 sites88 target enrollmentMarch 8, 2017
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Depression
- Sponsor
- Professor Julia Rucklidge
- Enrollment
- 88
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) women aged 16 years and over; 2\) 12\-24 weeks gestation; 3\) low risk singleton pregnancy; 4\) free from psychiatric medication for four weeks; 5\) score of 13 or more on the Edinburgh Postnatal Depression Scale (EPDS); 6\) deemed reliable and compliant with the protocol.
- •Reference group inclusion criteria:
- •1\) pregnant women aged 16 years and over; 2\) low risk singleton pregnancy
Exclusion Criteria
- •1\) regular vomiting; 2\) high risk pregnancy; 3\) significant pregnancy complications; 4\) known foetal abnormalities; 5\) serious current or historical medical condition; 6\) known allergy to the ingredients of the intervention; 7\) known metabolic condition such as Wilson’s disease, hemochromatosis.; 8\) untreated or unstable thyroid disease; 9\) known neurological disorder; 10\) desire to continue taking prenatal supplements that either exceed the upper limit or are not required for medical purposes (decisions discussed and made on a case\-by\-case basis)
Outcomes
Primary Outcomes
Not specified
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