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

Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo0 个研究点开始时间: 2022年5月23日最近更新: 2023年5月29日

适应症

试验速览

暂无简介。

•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

•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

发起方

Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo