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

Evaluating the effectiveness of a Brief Intervention for Post-traumatic stress disorder associated with childbirth/birth: a clinical, randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4yjvpxg
Enrollment
Unknown
Registered
2022-05-23
Start date
2022-07-04
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Depression postpartum

Interventions

The study will be conducted at the High-Risk Pregnancy Service of the Hospital das Clínicas, Faculty of Medicine of Ribeirão Preto, University of São Paulo, as this is a reference center in the city o
F04.754.715

Sponsors

Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo
Lead Sponsor
Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
To assess the presence/absence of post-traumatic stress disorder associated with childbirth, dentifying the prevalence among study participants—

Secondary

MeasureTime frame
Assess the presence/absence of depressive symptoms and postpartum/birth stress and their associations with birth situations;It is expected to identify the risk and protective factors associated with the onset of post-traumatic stress disorder associated with childbirth—

Countries

Brazil

Contacts

Public ContactMaira Borges

Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo

borges.mairam@gmail.com+ 55(16)996394131

Outcome results

None listed

Source: REBEC (via WHO ICTRP)