Student Paramedics' Experiences of Compassion Fatigue: a Phenomenological Mixed-methods Study
NCT ID: NCT06998602
Last Updated: 2025-06-04
Study Results
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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COMPLETED
7 participants
OBSERVATIONAL
2024-11-19
2025-02-17
Brief Summary
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To do this, a group of student paramedics were interviewed about their personal experiences and also asked to complete a short questionnaire called the Professional Quality of Life Scale (ProQOL). This questionnaire measured their levels of compassion satisfaction (positive feelings from helping others), burnout (emotional exhaustion), and secondary traumatic stress (stress from exposure to others' trauma).
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Detailed Description
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Participants were recruited from the BSc (Hons) Paramedic Practice programme at UK University, using purposive, non-probability sampling. Data collection involved two components:
1. Semi-structured interviews conducted online via Microsoft Teams to explore participants' lived experiences.
2. Completion of the Professional Quality of Life (ProQOL) questionnaire, which measured Compassion Satisfaction, Burnout, and Secondary Traumatic Stress.
Interview transcripts were analysed thematically using Braun and Clarke's six-step framework. The ProQOL data were analysed using descriptive statistics and inferential comparisons using both Frequentist and Bayesian analysis, using JASP software. The target sample size was between 3-10. Seven participants completed the study.
Eligible participants were contacted via email by the designated gatekeeper, the course leader. The email outlined that, as student paramedics who had attended clinical placement as part of their course, they were eligible to take part in the study. The email invited them to read the participant information sheet and contact the primary researcher with any questions. Those interested in participating were asked to get in touch to organise receipt of the informed consent form.
Following initial contact, the primary researcher corresponded with interested participants via email to arrange a suitable date and time for the interview. Depending on participant preference, interviews were conducted either on campus or via Microsoft Teams.
Conditions
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Study Design
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OTHER
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
18 Years
65 Years
ALL
Yes
Sponsors
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Teesside University
OTHER
Responsible Party
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Jonathan Robinson, Ph.D
Senior Lecturer in Research Methods
Locations
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Teesside University
Middlesbrough, , United Kingdom
Countries
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Other Identifiers
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24118
Identifier Type: -
Identifier Source: org_study_id
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