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临床试验/NCT03402074
NCT03402074已完成不适用

Group Hypnosis for Stress Reduction - a Feasibility Study

Charite University, Berlin, Germany1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2017年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
15
试验地点
1
主要终点
Cohens Perceived Stress Scale 10 Items

研究概览

简要总结

This prospective feasibility study aims to test a 5 week group hypnosis training as intervention to reduce perceived psychological stress in healthy subjects.

详细描述

In a pre- post comparison the feasibility of a standardized weekly 90 minutes group hypnosis training including CDs/MP3 recordings as homework to reduce perceived psychological stress in healthy subjects is investigated. Outcomes are measured quantitatively and qualitatively.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy or health-stable participants between 18 and 70 years with subjective increased intensity of stress in the last four weeks on the visual analogue scale rated between 40 -100 mm (VAS 0 - 100 mm)
  • Ability to consent and sign declaration of informed consent

排除标准

  • Current or planned participation in a stress management program within the next 17 weeks
  • Current use of psychotherapeutic treatment
  • presence of moderate or severe acute or chronic disease
  • presence of an acute or chronic mental disorder
  • Participation in a study within the last 2 months prior to enrollment
  • Lack of understanding of the German language

研究组 & 干预措施

Group Hypnosis

Experimental

5 sessions of group hypnosis, each 90 minutes; plus CDs/MP3 recordings to train at home

干预措施: Group hypnosis (Behavioral)

结局指标

主要结局

Cohens Perceived Stress Scale 10 Items

时间窗: 5 weeks

Likert-Skala

时间窗: 5 weeks

about stressreduction

ADS-K (Depression)

时间窗: 5 weeks

SF 36 Quality of Life

时间窗: 5 weeks

Perceived Stress on Visual Analogue Scale

时间窗: 5 weeks

VAS 0-100 mm

General Self Efficacy Scale (Schwarzer)

时间窗: 5 weeks

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Benno Brinkhaus

Prof. Dr. med.

Charite University, Berlin, Germany

研究点 (1)

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