- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica 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.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
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.
Tipo di studio
Iscrizione (Stimato)
Fase
- Non applicabile
Contatti e Sedi
Contatto studio
- Nome: Yu Gao, M.Ed.
- Numero di telefono: +601163686780
- Email: gaoyu89757@gmail.com
Backup dei contatti dello studio
- Nome: Wen Ting Tong, PhD
- Numero di telefono: 60166803231
- Email: tongwenting@um.edu.my
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
Accetta volontari sani
Descrizione
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
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Separare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: MET intervention
Participants in the intervention group will receive MET intervention during the trial.
|
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.
|
|
Nessun intervento: Waitlist control group
Participants assigned to the waitlist control group receive no study intervention during the trial period.
After completion of the final follow-up assessment, they will be offered the Moving to Emptiness Technique (MET).
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Compassion Fatigue
Lasso di tempo: Baseline, Week 4, Week 8
|
Chinese validated Compassion Fatigue Questionnaire (Source: Wang Junting, 2024)
|
Baseline, Week 4, Week 8
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Professional Quality of Life scale
Lasso di tempo: Baseline, Week 4, Week 8
|
Chinese validated Professional Quality of Life scale (Source: Zheng et al., 2013)
|
Baseline, Week 4, Week 8
|
|
Counselling Self-Estimate
Lasso di tempo: Baseline, Week 4, Week 8
|
Counselling Self-Estimate Inventory (Source: Yuen et al., 2004)
|
Baseline, Week 4, Week 8
|
Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Yew Kong Lee, PhD, Faculty of Medicine, Faculty of Medicine
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Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- UM.TNC(P&I)/UMREC/3/6535
Piano per i dati dei singoli partecipanti (IPD)
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Descrizione del piano IPD
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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