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临床试验/NCT04350333
NCT04350333Unknown不适用

Efficacy of Digital Cognitive Behavioral Therapy for Insomnia (CBT-I) Intervention During Pregnancy in Prevention of Post-partum Depression: a Randomized Clinical Trial

University of Rome G. Marconi0 个研究点目标入组 114 人开始时间: 2021年5月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
114
主要终点
Anxiety

研究概览

简要总结

This randomized controlled trial aims to evaluate the efficacy of Cognitive Behavioral Therapy for Insomnia in pregnant women. Particularly, this study aim to explore the effect of this intervention in ameliorating insomnia symptoms and in preventing post-partum depression disorder. The experimental intervention is a digital CBT-I and the control intervention group is an assertive communication training. Both interventions include a screening phase and will be delivered in a digital way and will be composed of 5 sessions. Furthermore, both interventions protocol include a baseline, half time and follow up assessments.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
19 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Healthy pregnancy
  • Women that not consume nicotine or alcool
  • BMI < 30
  • Women who complains of insomnia or bad sleep quality

排除标准

  • Complicated pregnancy
  • Women who consume nicotine or alcool

结局指标

主要结局

Anxiety

时间窗: Follow up: 6 months post partum

Anxiety symptomatology (State-trait anxiety inventory - STAI-Y). Higher scores mean a worse outcome.

Depression

时间窗: Follow up: 6 months post partum

Depression symptomatology (Edinburgh Postnatal Depression Scale - EPDS). Scoring: \< 8: depression not likely; 9-11: depression possible; 12-13:Fairly high possibility of depression; \> 14 probable depression

次要结局

  • Sleep pattern (sleep onset latency; total sleep time; wake after sleep onset; sleep efficiency)(Post intervention: after 5 weeks from the start of intervention)
  • insomnia symptoms(Post intervention: after 5 weeks from the start of intervention)
  • Emotion regulation(Post intervention: after 5 weeks from the start of intervention)

研究者

发起方
University of Rome G. Marconi
申办方类型
Other
责任方
Principal Investigator
主要研究者

Valeria Bacaro

Principal Investigator

University of Rome G. Marconi

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