- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05438745
The Effects of Dog Therapy on Ambulance Staff Burnout Scores. (Pawamedics)
Problem During the COVID 19 pandemic, NHS staff have become increasingly burned out. Mental health is the leading cause of staff sickness and absence in the NHS. Ambulance trusts have the highest rates of sickness across all NHS professions. Reduced staffing levels directly impacts service delivery. Staff struggling with poor mental health are more likely to make errors, have reduced empathy, and patients have lower patient satisfaction.
The Solution? Dog therapy is used in hospital settings around the world for patient benefit and staff welfare.
Evidence suggests dog therapy improves mood and reduces anxiety. Yorkshire Ambulance Service (YAS) has a small, but established dog therapy scheme, organised by the health and wellbeing team.
This research aims to observe if dog therapy affects symptoms of burnout in YAS staff. We will use two sets of staff:
Patient facing staff Staff with remote patient contact
What will participants need to do?
Participants will be given a Copenhagen Burnout Inventory - a questionnaire focusing on three factors:
Personal burnout Work related burnout Client related burnout
Burnout will be measured in 4 categories; no/low, moderate, high and severe burnout.
The questionnaire will be completed at the beginning and end of 8 weeks of dog therapy.
- Some optional demographic questions
- Number of sessions attended
- Engagement with occupational health services
- Dog Ownership
We will calculate the difference in severity of burnout between baseline and after 8 weeks of dog therapy.
A PPI group has been consulted on methodology, wording of plain English summary and the dissemination plan.
This research will be distributed to all interested participants, published in an appropriate journal presented at conferences, and presented in the ICA dissemination event.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Richard Pilbery, MSc
- Phone Number: +4407592269779
- Email: r.pilbery@nhs.net
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Yorkshire Ambulance Service (YAS) Employee with patient contact. Patient contact includes face to face to face or remote patient contact. Taking part in YAS dog therapy scheme. Completed no more than 2 dog therapy sessions to date. -
Exclusion Criteria:
Staff with no patient contact as part of their role. Staff on bank contract
-
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Experimental Group
Ambulance Service Staff participating in pet therapy sessions.
|
Questionnaire
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mean difference in change of each section of Copenhagen Burnout Inventory (CBI) Score
Time Frame: 8 weeks.
|
CBI will be measured at week 0 and week 8.
The CBI is composed of 3 sections.
We will calculate a mean change in score for each of the 3 sections.
|
8 weeks.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mean difference ambulance turnaround times.
Time Frame: 8 weeks.
|
We will calculate a mean difference in ambulance turnaround times for those participating in dog therapy vs those not participating on dog therapy.
|
8 weeks.
|
|
Drop out rate.
Time Frame: 8 weeks.
|
We will report the proportion of participants that withdraw from the study.
|
8 weeks.
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Richard Pilbery, MSc, Yorkshire Ambulance Service NHS Trust
Study record dates
Study Major Dates
Study Start (ANTICIPATED)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- YASRD170
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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