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临床试验/NCT07204535
NCT07204535招募中不适用

Post-TRaUmatic STress Disorder Induced by Gynecological Brachytherapy

Centre Paul Strauss3 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年11月17日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
80
试验地点
3
主要终点
Post-Traumatic Stress Disorder evaluation

研究概览

简要总结

This is a multicenter, prospective study aimed at providing information on the psychological effects (including post-traumatic stress symptoms) of utero-vaginal brachytherapy in patients with cervical cancer using self-administered questionnaires. The study also aims to assess the persistence of these symptoms over time, up to 5 years after brachytherapy. The results could help identify patients at risk of post-traumatic stress in this context and develop appropriate psychological interventions to improve their psychological well-being during and after treatment.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Confirmed diagnosis of cervical cancer with an indication for High-dose rate (HDR) or pulse-dose rate (PDR) uterovaginal brachytherapy;
  • Squamous cell carcinoma or other histological types;
  • Ability to complete validated questionnaires in French;
  • Informed consent to participate in the study;
  • Patients over 18 years old

排除标准

  • Inability to understand or respond to questionnaires due to a cognitive disorder, intellectual disability, language barrier, or psychiatric disorder that impairs judgment;
  • Patient under juridic protection;
  • Pregnant or breastfeeding woman

结局指标

主要结局

Post-Traumatic Stress Disorder evaluation

时间窗: at 2 months

Evaluation with post-traumatic stress disorder Checklist version DSM-5 (PCL-5) - questionnaire with a Cut off score ≥ 32

次要结局

  • Anxiety and Depression(until 60 months)
  • Quality of Life (general module)(until 60 months)
  • Quality of Life (cervical cancer module)(until 60 months)
  • Sexual Health evaluation(until 60 months)

研究者

发起方
Centre Paul Strauss
申办方类型
Other
责任方
Sponsor

研究点 (3)

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