NCT05637190

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

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2022

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

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

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

November 24, 2022

Completed
11 days until next milestone

First Posted

Study publicly available on registry

December 5, 2022

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2023

Completed
Last Updated

February 8, 2023

Status Verified

February 1, 2023

Enrollment Period

2 years

First QC Date

November 24, 2022

Last Update Submit

February 7, 2023

Conditions

Keywords

Expressive Arts TherapyTeachersRandomized controlled trial

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

EXPERIMENTAL

The 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.

Other: Expressive Arts Therapy group intervention

Waitlist control group

NO INTERVENTION

The 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.

Expressive Arts Therapy group

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

RECRUITING

MeSH Terms

Conditions

Burnout, Psychological

Condition Hierarchy (Ancestors)

Stress, PsychologicalBehavioral SymptomsBehavior

Study Officials

  • Fiona YY Ho, Ph.D

    Chinese University of Hong Kong

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Yeuk Yu Yip

CONTACT

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

Locations