Depression during pregnancy Pregnancy and Childbirth Mental disorders and diseases of the nervous system complicating pregnancy, childbirth and the puerperium
Conditions
Interventions
Group 1 (Intervention arm plus usual care):
Involvement in the study will last 33 weeks. Patients will be invited to attend up to 12 once weekly one-to-one CBT sessions, 60 minutes per sessions. Thes
Sponsors
University of Bristol (UK)
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Pregnant women in North Bristol 2. Aged 16 or over 3. Between 8 and 18 weeks pregnant 4. Screen positive on the three question depression screen 5. Meet criteria for International Classification of Diseases, version 10 (ICD-10) depression (assessed using the Clinical Interview Schedule - Revised [CIS-R] version)
Exclusion criteria
Exclusion criteria: 1. Currently receiving CBT or another individual psychological therapy 2. Known to have a psychotic illness 3. Receiving care from secondary mental health services 4. Do not have sufficient English to complete questionnaires, as translation might affect the validity of the scales, and they would not be able to benefit from a talking therapy without an interpreter 5. Taking part in any other intervention trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| CIS-R diagnosis, conducted at baseline, 1st follow-up (15 weeks post-randomisation), and 2nd follow-up (33 weeks post-randomisation). | — |
Secondary
| Measure | Time frame |
|---|---|
| Other symptom measures (e.g. EPDS, PHQ-9, SF-12, EQ-5D), conducted at baseline, 1st follow-up (15 weeks post-randomisation), and 2nd follow-up (33 weeks post-randomisation). | — |
Countries
United Kingdom
Outcome results
None listed