Ireland
--:--IST
Enrolling by invitation Not applicable

Decrease Caregiving Fatigue in Group Leaders of a Support Group for Women After Cancer

NCT06937606 · tracked via the Priya Life Science Germany tracker
Phase
Not applicable
Started
2024-07-31
Last updated
2025-04-22

Condition(s) studied

Caregiver Burden

Investigational drug(s) / intervention(s)

Self-compassion training

Self-compassion training: 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);

Study summary

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

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Group leaders of a self-help group for cancer patients * written informed consent Exclusion Criteria: * 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

Primary outcome measure(s)

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

Trial sites (1)

FacilityCityRegionStatus
Comprehensive Cancer Center Würzburg Würzburg Bavaria

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06937606 on ClinicalTrials.gov ↗ ← All trials in Germany