跳至主要内容
临床试验/NCT06937606
NCT06937606Enrolling By Invitation不适用

A Randomized, Controlled Trial to Increase Self-compassion and Decrease Caregiving Fatigue in Group Leaders of a Support Group for Women After Cancer (GLOW) - an Adaption of the Mindful Self-Compassion Program for Healthcare Communities

Wuerzburg University Hospital1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2024年7月31日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
64
试验地点
1
主要终点
self-compassion as assessed by Self-compassion scale in german version (SCS-D)

研究概览

简要总结

This exploratory study aims to evaluate the effect of a self-compassion training developed for health professionals on leaders of self-help groups.

Hypothesis/primary goal: An online group intervention adapted from the "Self-compassion for health-care communities program" validated for health professionals leads to an increase in self-compassion among leaders of cancer self-help groups. Secondary goals: level of self-compassion at the end of the course as a mediator for therapeutic variables after 6 weeks, decrease in caregiver fatigue, secondary traumatic stress/burnout risk, personal distress and sick leave, decrease in fears of self-compassion/compassion for others; increase in mindfulness, self-efficacy, compassion for others and resilience; direct costs; safety;

Intervention:

Online group intervention: led by a certified mindfulness teacher for Mindful Self-Compassion and additional qualification in Self-Compassion in Healthcare Communities (duration: 6 weekly appointments of 90 min each); control intervention: waiting group

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
None

入排标准

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

入选标准

  • •Group leaders of a self-help group for cancer patients
  • •written informed consent

排除标准

  • •Medical or mental condition that, in the opinion of the investigator, does not allow the participant to take part in the study or to provide a legally valid signature of the informed consent (e.g. insufficiently controlled pre-existing mental illness or post-traumatic stress disorder)
  • •Lack of willingness to store and share personal health data as part of the protocol
  • •Participation in another mindfulness study
  • •Lack of knowledge of German

研究组 & 干预措施

Self-compassion training

Experimental

Online group intervention: led by a certified mindfulness teacher for mindful self-compassion and additional qualification in self-compassion in healthcare communities (duration: 6 weekly appointments of 90 min each);

干预措施: Self-compassion training (Behavioral)

waiting list control

No Intervention

waiting list control

结局指标

主要结局

self-compassion as assessed by Self-compassion scale in german version (SCS-D)

时间窗: 6 weeks after baseline

Determining self-compassion after the intervention by means of a confirmatory test for group differences in the primary endpoint according to the ITT principle using a linear regression model; instrument: SCS-D

次要结局

  • secondary traumatic stress/burnout risk as assesd by ProQoL(12 weeks after baseline)
  • Decrease in compassion fatigue as assessed by ProQoL(12 weeks after baseline)
  • personal distress (PSS-10)(12 weeks after baseline)
  • increase in resilience (BRS)(12 weeks after baseline)
  • Number of participants with treatment-related adverse events as assessed by CTCAE v4.0(12 weeks after baseline)
  • decrease in fears of self-compassion (FCS)(12 weeks after baseline)
  • compassion for others (COS-7)(12 weeks after baseline)
  • increase in mindfulness (FFMQ)(12 weeks after baseline)
  • increase in self-efficacy (SWE)(12 weeks after baseline)

研究者

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

Dr. Claudia Loeffler

PD Dr. med., Senior physician

Wuerzburg University Hospital

研究点 (1)

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