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Art Therapy to Address Hospital Clinician Burnout

Art Therapy to Address Hospital Clinician Burnout and Psychosocial Distress: a Randomised Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05728086
Acronym
CHArt
Enrollment
131
Registered
2023-02-14
Start date
2023-03-06
Completion date
2024-03-05
Last updated
2024-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Burnout, Depression, Stress

Keywords

Art therapy, psychosocial distress, hospital clinicians, burnout

Brief summary

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

Detailed description

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).

Interventions

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.

Sponsors

Queen Mary University of London
CollaboratorOTHER
Barts & The London NHS Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Intervention model description

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

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Change in burnout element 'Emotional Exhaustion' assessed using the Emotional Exhaustion scale of The Maslach Burnout Inventory - Human Services Survey (MBI-HSS)Baseline [T1], post 6-week intervention / post 6-week wait [T2], 12 week post intervention follow up [T3]The MBI-HSS assesses three elements of burnout syndrome: emotional exhaustion, depersonalization, and lack of personal accomplishment. Each element is measured by a separate scale. The Emotional Exhaustion (EE) scale assesses feelings of being emotionally over-extended and exhausted at work. It includes 9 items which are scored on a 7-item Likert scale from 0 = never to 6 = every day. The scale has a score range of 0-54 with higher scores corresponding to greater experiences of burnout.

Secondary

MeasureTime frameDescription
Change in burnout element 'personal accomplishment' assessed using the Personal Accomplishment scale of The Maslach Burnout Inventory - Human Services Survey (MBI-HSS)Baseline [T1], post 6-week intervention / post 6-week wait [T2], 12 week post intervention follow up [T3]Personal Accomplishment (PA) scale assesses feelings of competence and achievement in work with people. It includes 8 items which are scored on a 7-item Likert scale from 0 = never to 6 = every day. The scale has a score range of 0-48 with lower scores corresponding to greater experiences of burnout.
Change in anxiety assessed using the Generalised Anxiety Disorder Questionnaire (GAD 7)Baseline [T1], post 6-week intervention / post 6-week wait [T2], 12 week post intervention follow up [T3]The GAD 7 assesses anxiety. It includes 7 items which are scored on a 4-item Likert scale from 0 = not at all to 3 = nearly every day. The scale has a score range of 0-21 with higher scores corresponding to greater levels of anxiety.
Change in burnout element 'depersonalisation' assessed using the Depersonalisation scale of The Maslach Burnout Inventory - Human Services Survey (MBI-HSS)Baseline [T1], post 6-week intervention / post 6-week wait [T2], 12 week post intervention follow up [T3]Depersonalisation scale of the MBI - HSS The 5-item Depersonalization (DP) scale assesses an emotionally distant / indifferent response toward patients. It includes 6 items which are scored on a 7-item Likert scale from 0 = never to 6 = every day. The scale has a score range of 0-30 with higher scores corresponding to greater experiences of burnout.
Change in perceived stress assessed using the Perceived Stress Scale (PSS-10)Baseline [T1], post 6-week intervention / post 6-week wait [T2], 12 week post intervention follow up [T3]The PSS10 assesses perceived stress. It includes 10 items which are scored on a 5-item Likert scale from 0 = never to 4 = very often. The scale has a score range of 0-40 with higher scores corresponding to greater levels of perceived stress.
CHArt Feedback Questionnairepost 6-week intervention [T2]This is a participant experience feedback questionnaire. It includes 8 items on themes of perceived helpfulness, perceived behavioural change and attribution of change, barriers and enablers to attendance. Questions include multiple choice and follow - up free text elements. For example Question 6: Were there any barriers / challenges to attending? Yes, definitely; Yes, some; Not really; Not at all If so, what were they and how did you address them? If not, what made attendance possible for you?
Change in depression assessed using the Personal Health Questionnaire Depression Scale (PHQ 8)Baseline [T1], post 6-week intervention / post 6-week wait [T2], 12 week post intervention follow up [T3]The PHQ 8 assesses severity of depression. It includes 8 items which are scored on a 4-item Likert scale from 0 = not at all to 3 = nearly every day. The scale has a score range of 0-24 with higher scores corresponding to greater severity of depression.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026