Effects of a Group Intervention to prevent Post-traumatic stress disorder linked to childbirth: a comparative study between two groups of high-risk pregnant wome

Not Applicable

• Conditions: Depression postpartum; Pregnancy High-Risk; F03.950.750.500

• Registration Number: RBR-4yjvpxg
• Lead Sponsor: Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-05-23
• Last Update Posted: 29 May 2023
• Study Completion: 2025-12-19

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

The pregnant women must be 18 years of age or older; being in the third trimester of pregnancy (between 28 and 32 weeks of gestation); no history of previous (self-reported) mental disorders, except for common mental disorders and current ones (score on the Self Report Questionnaire less than 7), score on the Health Questionnaire of the Patient-9 less than 10 and General Anxiety Disorder Questionnaire-7 score less than 10; not being in psychological and psychiatric treatment at the time of data collection; and agree to voluntary participation in the study, signing the Free and Informed Consent Form

Exclusion Criteria

Women who drop out of the study at any stage of data collection before the conclusion of the same; do not attend the sessions for the application of the assessment instruments or the meetings of the intervention group, regardless of the reason; and are not found after the pregnancy is resolved by the telephone and/or e-mail provided by them for the evaluation of outcomes

Study & Design

• Study Type: Intervention
• Study Design: Not specified