Assessment of Childbirth-Related Post-Traumatic Stress Disorder (SSPT-A)
Assessment of Childbirth-Related Post-Traumatic Stress Disorder: A Single-Center Prospective Study
研究概览
地位
详细说明
Secondary objectives
To identify risk factors associated with the development of PTSD, in order to determine which situations-particularly obstetric ones-could lead women to experience trauma, and understand the underlying psychological mechanisms.
Risk factors identified in the literature or deemed relevant by the study's clinicians and psychologists will be gathered from medical records.
- To assess healthcare utilization in the context of the onset of childbirth-related PTSD from the women's perspective, using a questionnaire consisting of a series of questions about the different healthcare professionals consulted during the month following childbirth.
Conduct of research About one month after giving birth, women who have provided their consent will receive an email containing a personal link to the eCRF page where they will find the French version of the "City Birth Trauma Scale" (CBTS) questionnaire, as well as the questionnaire designed to assess their use of healthcare services.
After completing the CBTS questionnaire, the participant can choose to check a box in the eCRF to indicate whether or not she wishes to be contacted by the research team in the event that her score suggests a diagnosis of PTSD.
If the participant has not completed the questionnaire within 10 days of receiving the link, a follow-up email will be sent to her. If, after receiving this follow-up email, the participant has not completed the questionnaire or contacted the research team, she will be considered lost to follow-up.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Edgar Yohny Montoya Ramirez, MD
- 电话号码:+33 3 89 64 64 64
- 邮箱:montoyaramireze@ghrmsa.fr
学习地点
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Mulhouse、法国、68100
- Groupe Hospitalier de la Région de Mulhouse et Sud Alsace
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion criteria:
- Women aged 18 or older
- Having given birth in the maternity ward at Emile Muller Hospital (Mulhouse, Haut-Rhin, France)
- Fluent in French
- Having provided written consent to participate in the study
- Being covered by a social security program
Exclusion Criteria:
- Women who gave birth anonymously
- Women who gave birth to a stillborn child or a fetus that died in utero
- Women under legal protection (guardianship, conservatorship, judicial protection).
学习计划
研究是如何设计的?
设计细节
- 主要用途:其他
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
其他:Women who have given birth within the past month
|
About one month after giving birth, patients who have given their consent will receive an email containing a personal link to the eCRF page with the French version of the City Birth Trauma Scale (CBTS) questionnaire, as well as a questionnaire to assess their use of healthcare services. After completing the CBTS questionnaire, the participant can choose to check a box in the eCRF to indicate whether or not she wishes to be contacted by the research team in the event that her score suggests a diagnosis of PTSD. |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
City Birth Trauma Scale
大体时间:About 1 month after childbirth
|
The diagnosis of PTSD based on responses to the questionnaire will be made in accordance with the questionnaire's scoring method, which assesses 8 criteria based on the DSM-5 (criteria labeled A through H).
|
About 1 month after childbirth
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Questionnaire on the assessment of healthcare utilization
大体时间:About 1 month after childbirth
|
A ten-item questionnaire to assess the use of healthcare services in the context of postpartum post-traumatic stress disorder from the women's perspective, enquiring about the healthcare professionals these women consulted during the month following childbirth.
|
About 1 month after childbirth
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- GHRMSA 1497
- ID-RCB 2026-A00733-48 (其他标识符:Agence nationale de sécurité du médicament et des produits de santé)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
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