Art Therapy to Address Hospital Clinician Burnout

NCT ID: NCT05728086

Last Updated: 2024-03-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

131 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-03-06

Study Completion Date

2024-03-05

Brief Summary

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A structured group art therapy intervention, comprising six 60 - 90-minute weekly workshops.

Detailed Description

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The CHArt group art therapy intervention builds on a 6-week art therapy group intervention piloted with Barts Health oncology and palliative care doctors (Tjasink, M. 2019). It incorporates elements of workshops delivered for staff support by Barts art therapists during the Covid-19 pandemic (Tjasink, M., Stevens, P. 2022).

The intervention is broadly informed by affective neuroscience and evolutionary psychology theories with an emphasis on compassion-focused and resource-oriented therapeutic practice. Whilst the intervention draws on diverse influences, it aligns with the principles of Compassion Focussed Therapy (CFT), an integrative, bio-physiological psychological model underpinned by evolutionary theory.

Intervention elements include psycho-education, individual art making, collaborative group art making, art making in pairs, exploring a range of art materials and techniques (including clay, paint, natural objects and non-traditional mark - making materials), art-based grounding exercises and reflective discussion.

The intervention manual was developed by the study's Chief Investigator with input from a group of three art therapy experts (Health and Care Professions Council (HCPC) accredited art therapists working in National Health Service (NHS) medical contexts with experience of delivering art therapy - based staff support) and three experts by experience (Health Care professionals with experience of participating in art therapy - based staff support groups at work). Adherence to the intervention will be monitored through two adherence tools (therapist self reported and independent observer).

Conditions

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Burnout Anxiety Stress Depression

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Waitlist randomized controlled trial (RCT) design comprising an intervention group and a waitlist-control group
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Group art therapy

Participants randomised to the intervention group receive the group art therapy intervention shortly after baseline assessment. Adherence to the intervention will be checked via an adherence questionnaire completed by therapist delivering the intervention after each session. In addition, 20% of sessions will be observed by an independent researcher for adherence checking.

Group Type EXPERIMENTAL

Group art therapy

Intervention Type OTHER

The intervention is a manualised programme of group art therapy based on a bio-psychosocial therapeutic model. The programme is made up of six 60 - 90-minute art therapy group sessions facilitated by an experienced HCPC (Health and Care Professions Council) registered Art Therapists trained in the intervention.

waitlist control group

Participants randomised to the waitlist control group will complete outcomes measures at baseline and at the end of a 6 week waiting period. They will then begin the intervention (1-2 weeks after the intervention group has finished).

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Group art therapy

The intervention is a manualised programme of group art therapy based on a bio-psychosocial therapeutic model. The programme is made up of six 60 - 90-minute art therapy group sessions facilitated by an experienced HCPC (Health and Care Professions Council) registered Art Therapists trained in the intervention.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* • Healthcare professional employed in a patient facing clinical role by Barts Health NHS Trust or Barts Bank partners

* 18 years or older
* Willing and able to provide informed consent
* Able to attend the group intervention sessions
* Moderate to severe risk scored on any of the three MBI - HSS subscales or on the PSS 10:
* emotional exhaustion score of ≥17, or
* depersonalization score of ≥7, or
* personal accomplishment score of ≤ 38 or
* perceived stress (≥ 14)

Exclusion Criteria

* • Unwilling or unable to give consent

* Diagnosed with or treated for a serious depressive condition, a personality disorder or psychosis in the past 12 months. (Self-reporting through screening.)
* Attempted suicide or made plans to commit suicide in the past 12 months. (Self-reporting through screening.)
* Individual does not provide direct patient care for Barts Health NHS Trust
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Queen Mary University of London

OTHER

Sponsor Role collaborator

Barts & The London NHS Trust

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Stefan Priebe

Role: STUDY_CHAIR

Queen Mary University of London

Locations

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Barts Health NHS Trust

London, , United Kingdom

Site Status

Countries

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United Kingdom

References

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Tjasink, M., G. Soosaipillai (2019) Art therapy to reduce burnout in oncology and palliative care doctors: a pilot study.

Reference Type BACKGROUND

Tjasink, M, Stevens, P. (2022). The innovative use of art psychotherapy with NHS clinicians in Jury, H. and Coles, A., 'Art Psychotherapy and Innovation: New Territories, Techniques and Technologies'. Jessica Kingsley, London: 83 - 103.

Reference Type BACKGROUND

Maslach, C. et al. (2018). Maslach burnout inventory: manual. [Menlo Park, Calif.], Mind Garden.

Reference Type BACKGROUND

Tjasink M, Carr CE, Bassett P, Soosaipillai G, Ougrin D, Priebe S. Art therapy to reduce burnout and mental distress in healthcare professionals in acute hospitals: a randomised controlled trial. BMJ Public Health. 2025 Aug 3;3(2):e002251. doi: 10.1136/bmjph-2024-002251. eCollection 2025.

Reference Type DERIVED
PMID: 40761359 (View on PubMed)

Provided Documents

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Document Type: Informed Consent Form

View Document

Other Identifiers

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316097

Identifier Type: -

Identifier Source: org_study_id

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