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Cancelled by the investigator The Effect of Local Psychotherapy in Reducing Counselors’ Compassion Fatigue

The Effect of Local Psychotherapy in Reducing Counselors’ Compassion Fatigue

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122874
Enrollment
Unknown
Registered
2026-04-20
Start date
2026-04-27
Completion date
Unknown
Last updated
2026-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

compassion fatigue

Interventions

Experimental group::Received standardized air transfer technology intervention, implemented by trained researchers according to a unified operating procedure. The intervention period is 4 weeks, once
Control group::received routine psychological support meditation intervention, including breathing awareness, body scanning, mindfulness meditation, and returning to the present moment. The interventi

Sponsors

The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 18-60 years old; 2. Engaged in psychological counseling work for at least 1 year (including personal practicing psychological counselors, school, institution or hospital psychological counselors, intern psychological counselors, etc.); 3. Self reporting a certain degree of empathy fatigue, emotional exhaustion, or a need to prevent empathy fatigue; 4. Good Chinese comprehension ability, able to complete assessments and interventions; 5. Voluntarily participate in the research and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Currently undergoing other psychological treatments or psychiatric interventions (such as antidepressants, anti anxiety drugs, etc.); 2. Diagnosed with severe emotional disorders or mental illnesses (as assessed or self-reported by researchers); 3. Recently experienced major emergencies (such as bereavement, divorce, severe trauma) that may affect the experimental results; 4. Unable to guarantee timely participation in each intervention (4 weeks) or assessment (T0, T1, T2); 5. Participants include students of the researcher, supervisors, and other related parties who may affect the fairness of the research (to avoid ethical conflicts).

Design outcomes

Primary

MeasureTime frame
Compassion fatigue;

Secondary

MeasureTime frame
Burnout;counseling self-estimate;

Countries

China

Contacts

Public ContactGAO YU

The First Affiliated Hospital of Guangzhou University of Chinese Medicine

gaoyu89757@gmail.com+86 188 2271 4402

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026