A Pilot RCT on the Effect of ExAT on Teacher Burnout and Stress
The Effect of Expressive Art Therapy on Teacher Burnout and Stress: A Pilot Randomized Controlled Trial
1 other identifier
interventional
90
1 country
1
Brief Summary
The objective of this pilot randomized controlled trial is to evaluate the effects of Expressive Art Therapy on reducing burnout and stress symptoms among Hong Kong's primary and secondary school teachers. The proposed study is a pilot randomized controlled trial. Prior to all study procedures, 90 participants (i.e., primary and secondary school teachers) will be recruited to complete an online informed consent with telephone support. Eligible participants will be randomly assigned to either the Expressive Arts Therapy group (ExAT group) or the waitlist control group (WL group) in a ratio of 1:1. The ExAT group will receive the Expressive Arts intervention via face-to-face workshops for 2 consecutive weeks (2 hours per session). There are a total of 3 batches (around 15 participants per batch) for the intervention. Participants in this group will be in touch with their inner selves and inner resources via body movement, writing and music. There will be visual art creation as a conclusion for integrating the body and mind. The art products would be placed in their workplace for stress regulation. The WL control group will not receive any intervention during the study, but they will receive self-help art therapy materials after the whole study procedure. The outcome measures include burnout, stress, depressive, and anxiety symptoms, as well as insomnia symptoms, physical activity, health-related quality of life, and the intervention acceptability at baseline, immediate post-treatment, and 4-week follow-up assessments by completing the same questionnaire set.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2022
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 10, 2022
CompletedFirst Submitted
Initial submission to the registry
November 24, 2022
CompletedFirst Posted
Study publicly available on registry
December 5, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2023
CompletedFebruary 8, 2023
February 1, 2023
2 years
November 24, 2022
February 7, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Changes in Shirom-Melamed Burnout Measure (SMBM)
A 14-item questionnaire with 7-point scale will be used for physical fatigue, emotion exhaustion, and cognitive weariness. The score ranges from 1(never or almost never) to 7 (always or almost always). Item 1-5: physical fatigue; item 6-8: emotional exhaustion; and item 9-14: cognitive wariness
baseline (week 0), immediate post intervention (week 3) and 4-week post intervention follow up
Change in Perceived Stress Scale (PSS)
A 10-item questionnaire measuring the perceived degree of stress across situations over the past month. Items include how unpredictable, uncontrollable, and overloaded do the respondents perceive. the score ranges from 0 (never) to 4 (very often)
baseline (week 0), immediate post intervention (week 3) and 4-week post intervention follow up
Secondary Outcomes (7)
Change in The Patient Health Questionnaire (PHQ-9)
baseline (week 0), immediate post intervention (week 3) and 4-week post intervention follow up
Change in The Generalized Anxiety disorder 7-item Scale (GAD-7)
baseline (week 0), immediate post intervention (week 3) and 4-week post intervention follow up
Change in Insomnia Severity Index (ISI)
baseline (week 0), immediate post intervention (week 3) and 4-week post intervention follow up
Change in Multidimensional Fatigue Inventory (MFI-20)
baseline (week 0), immediate post intervention (week 3) and 4-week post intervention follow up
Change in Short Form (Six-Dimension) Health Survey - The Chinese (Hong Kong) Version (SF-6D)
baseline (week 0), immediate post intervention (week 3) and 4-week post intervention follow up
- +2 more secondary outcomes
Study Arms (2)
Expressive Arts Therapy group
EXPERIMENTALThe Expressive Arts Therapy group will receive the Expressive Arts intervention via face-to-face workshops for 2 consecutive weeks (2 hours per session). there are a total of 3 batches (around 15 participants per batch) for the intervention.
Waitlist control group
NO INTERVENTIONThe Waitlist control group will not receive any intervention during the study, but they will receive self-help art therapy materials after the whole study procedure.
Interventions
Art is helpful to reduce negative emotions and boost self-worth during the creative process. During the Expressive Arts Therapy workshops, participants experience different art forms, including visual art, body movement, writing, music, and guided imagery to identify the inner self and get in touch with the self to release suppressed emotions and stress.
Eligibility Criteria
You may qualify if:
- Hong Kong residents aged \>/=18
- Able to read Chinese (verbal expression in Chinese or English)
- With qualified teaching cert. (degree holder)
- Willing to provide informed consent and comply with the trial protocol
- Teacher work in primary or secondary school in Hong Kong
You may not qualify if:
- Current involvement in psychological treatment program for stress and / or burnout reduction
- A change in psychotropic drugs or over-the-counter medications that target mood within 2 weeks before the baseline assessment
- A Patient Health Questionnair-9 (PHQ-9) item 9 score \> 2 indicating a serious level of suicidal risk
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Chinese University of Hong Kong
Hong Kong, HKSAR, Hong Kong
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Fiona YY Ho, Ph.D
Chinese University of Hong Kong
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
November 24, 2022
First Posted
December 5, 2022
Study Start
January 10, 2022
Primary Completion
December 31, 2023
Study Completion
December 31, 2023
Last Updated
February 8, 2023
Record last verified: 2023-02
Data Sharing
- IPD Sharing
- Will not share