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NCT Number: NCT07718035

Evaluating the Effectiveness of the Moving to Emptiness Technique in Reducing Counsellors' Compassion Fatigue

The goal of this clinical trial is to learn if Moving to Emptiness Technique (MET) works to treat counselors' compassion fatigue (CF). It will also learn about the effectiveness of MET on counselors' professional quality of life and counselling self-estimate. The main questions it aims to answer are:

• Does MET reduce counselors' compassion fatigue? Researchers will compare MET intervention to a waitlist control group to see if MET works to treat counselor burnout.

Participants will:

* Receive MET intervention for 4 sessions, once a week, 50 minutes per session. * Fill the questionnaires tests at three timepoints: before the intervention, immediately after the intervention phase and 4 weeks after the intervention.

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Key information

About this study

Compassion fatigue (CF) is a type of caregiver burnout which is developed by those persons who interact with traumatized individuals. Psychological counsellors are at high risk of CF. Interventions for counsellors' CF from former research included mindfulness-based interventions, and group psychotherapy. Moving to emptiness technique (MET) is a native Chinese psychotherapy, targeting to eliminate negative physical and emotional symptoms. MET is effective for many mental illness and physical symptoms, including depression, agoraphobia, insomnia, back pain caused by ankylosing spondylitis. However, the effectiveness of MET in alleviating counsellors' CF has not been empirically studied. Thus, this study aims to explore the effectiveness and feasibility of the MET intervention on CF among psychological counsellors, and to explore the effectiveness of MET on additional outcomes including professional quality of life and counselling self-estimate.

Participants will be recruited using convenience sampling through online channels relevant to psychological counsellors, including social media, professional forums and WeChat groups. Participants will also be recruited through peer networks whereby researchers' colleagues will be invited to share the study information within their professional circles. Recruitment will be initiated by distributing an online study invitation containing a brief overview of the research and a link to the participant information sheet through Wenjuan Xing. Individuals who express interest will be directed to the main researcher from whom they will receive detailed study information, complete the initial eligibility screening, and provide informed consent electronically. Eligible participants will then be scheduled for an online interview to confirm inclusion and exclusion criteria. All recruitment, screening, and enrolment procedures will be conducted remotely to accommodate participants' availability and ensure accessibility for practitioners across locations.

This study is a four-week two-armed trial. One group will receive the MET therapy (intervention group) and the other group (waitlist control group) will have their usual care while being on a waitlist and will participate in MET therapy after the trial is over. After registration, participants need to fill out a personal information questionnaire and a pre-test questionnaire first. Then, they will be randomly assigned to the intervention group or control group. After 4 weeks, participants will need to take another post-test, and after another 4 week, they will fill out the tracking questionnaire. This study will take 2 months, with 4 weeks' intervention stage and 4 weeks' tracking effectiveness stage. Participants in the intervention group are required to participate in a 4-week online intervention using MET (once a week and 50 minutes for each session) and fill out personal information questionnaires and test questionnaires. The MET sessions will be conducted by trained MET professional counsellors. Participants in the waitlist control group also need to fill out personal information questionnaires and test questionnaires but will proceed with your usual care. After the trial is over, they will have an opportunity to receive the same 4-week online MET as the experimental group.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults (aged 18-60)
  • Counsellors who have worked in the counselling profession for at least one year
  • Counsellors who self-report experiencing CF symptoms
  • Able to commit to attend the 4 weekly online sessions of 50 minutes' duration
  • Counsellors based in China

Exclusion criteria

  • Counsellors have received psychological therapy for their CF within the last 6 months
  • Counsellors who intend to participate in other psychological therapy for their CF besides MET during the study duration
  • Counsellors who self-report experiencing a traumatic event within past one year
  • Counsellors who self-report severe mental illness within past one year

Treatment and study plan

Moving to Emptiness Technique (MET)

Behavioral

The intervention is Moving to Emptiness Technique (MET), a native Chinese psychotherapy that integrates traditional Chinese cultural beliefs which focusses on the importance of the inner (psychological) world while including somatic (bodily) relaxation and the operational process of cognitive behavioural therapy. The delivery of MET intervention would be once a week, 50 minutes per session, across 4-weeks, to ensure the participants have enough rest between each session.

Primary outcomes

  1. Compassion Fatigue

    Time frame: Baseline, Week 4, Week 8

    Chinese validated Compassion Fatigue Questionnaire (Source: Wang Junting, 2024)

Secondary outcomes

  1. Professional Quality of Life scale

    Time frame: Baseline, Week 4, Week 8

    Chinese validated Professional Quality of Life scale (Source: Zheng et al., 2013)

  2. Counselling Self-Estimate

    Time frame: Baseline, Week 4, Week 8

    Counselling Self-Estimate Inventory (Source: Yuen et al., 2004)

Study contacts

Contact information is provided by the study sponsor or research team.

Wen Ting Tong, PhD

CONTACT

[email protected]

60166803231

Yu Gao, M.Ed.

CONTACT

[email protected]

+601163686780

Sponsors and collaborators

Lead sponsor

University of Malaya

Other

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jul 21, 2026
Registry last updated
Jul 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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