RecruitingACTRN12607000397415

Beating the Blues before Birth

Beating the Blues before Birth: Evaluating an Antenatal Depression Treatment Model as a Public Health Priority


Sponsor

Parent-Infant Research InstituteAustin Health

Enrollment

100 participants

Start Date

Jul 5, 2007

Study Type

Interventional

Conditions

Summary

Antenatal depression (AND) is at least as prevalent as postnatal depression and is an important risk factor for postnatal depression. Depression has major implications for women's well-being and for the health and well-being of their babies. Despite more than 1 in 10 women being affected by a clinical depression in pregnancy, treatment following identification is not part of routine antenatal care services. This study will test whether an 8 session cognitive behavioural group therapy program will reduce antenatal depression, anxiety and increase health service uptake compared to pregnant women not receiving the program. 100 women with a clinical diagnosis for depression will be randomised to either intervention or control group. Participants will be assessed by self-administered questionnaires pre and post treatment and at 3,6 and 12 month follow-up time points.


Eligibility

Sex: FemalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This study is testing whether a group therapy program using cognitive behavioural therapy (CBT) — a type of talk therapy that helps change unhelpful thought patterns — can help pregnant women who are experiencing depression. Depression in pregnancy (called antenatal depression) is just as common as depression after birth, and it can affect both the mother and the baby. The 8-session group program is being compared to usual care to see if it reduces depression and anxiety and helps women access health services. Participants will be followed up for 12 months after the program. You may be eligible if: - You are a woman aged 18 years or older - You are between 20 and 30 weeks pregnant - You have been diagnosed with minor or major depression (using standard DSM-IV diagnostic criteria) You may NOT be eligible if: - You are unable to understand written English - You have a major health problem affecting your ability to participate - You have a serious psychiatric condition such as psychotic depression that affects your ability to give informed consent - Your situation requires immediate crisis management - You are already participating in another psychological treatment program Talk to your doctor about whether this trial might be right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Intervention group is allocated to 8 sessions of a cognitive behavioural therapy group program and networked with health professionals. Each weekly session runs for an hour and a half and it is expect

Intervention group is allocated to 8 sessions of a cognitive behavioural therapy group program and networked with health professionals. Each weekly session runs for an hour and a half and it is expected that women attend every session. Women in this condition will be case-managed by a midwife/health professional and referred to other agencies/services as necessary, as normally happens where specialised programs are not available.


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ACTRN12607000397415


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