- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06998602
- Original Trial
Student Paramedics' Experiences of Compassion Fatigue: a Phenomenological Mixed-methods Study
This study explored how student paramedics experience compassion fatigue - a type of emotional and physical exhaustion that can occur when regularly caring for others in distress. The researchers wanted to understand how student paramedics feel about compassion fatigue, how it affects their work, and what kind of support might help them cope.
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).
Study Overview
Status
Detailed Description
This was a non-interventional, observational, mixed-methods study that used a phenomenological approach to explore student paramedics' experiences and perceptions of compassion fatigue (CF). The study aimed to identify how CF manifests during training, how it affects clinical practice, and which forms of support students believe would be helpful in preventing or managing CF.
Participants were recruited from the BSc (Hons) Paramedic Practice programme at UK University, using purposive, non-probability sampling. Data collection involved two components:
- Semi-structured interviews conducted online via Microsoft Teams to explore participants' lived experiences.
- 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.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Middlesbrough, United Kingdom
- Teesside University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Participants will be eligible if they are a current Student Paramedic, studying at target University and have attended clinical placement.
Exclusion Criteria:
- There is no exclusion criteria other than mental capacity.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Themes related to student paramedics' experiences of compassion fatigue
Time Frame: Interviews were completed at a single time point, depending on when the voluntary participant joined the study (between the 19th November 2024 and 13th December 2024).
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Key qualitative themes derived from semi-structured interviews with student paramedics, using Braun and Clarke's six-step thematic analysis framework.
Themes will reflect participants' lived experiences, perceptions, and coping mechanisms related to compassion fatigue.
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Interviews were completed at a single time point, depending on when the voluntary participant joined the study (between the 19th November 2024 and 13th December 2024).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Compassion Satisfaction score (ProQOL)
Time Frame: The questionnaire was completed at a single time point, depending on when the voluntary participant joined the study, post-interview (between the 19th November 2024 and 13th December 2024).
|
Self-reported scores on the Compassion Satisfaction subscale of the Professional Quality of Life Scale (ProQOL), version 5, and questions are scored on a scale of 1 to 5, and raw scores range between 10 to 50. Higher scores indicate greater compassion satisfaction, representing a more favourable outcome. ProQOL questionnaire, was scored according to the official ProQOL scoring guidelines. The ProQOL is a validated measure with acceptable internal consistency across its subscales, commonly used to assess compassion fatigue and related constructs in healthcare professionals. Descriptive statistics (mean and standard deviation) were calculated. If appropriate, to explore potential sex differences, statistical comparisons were conducted using both Frequentist and Bayesian approaches, with analyses performed in JASP software. |
The questionnaire was completed at a single time point, depending on when the voluntary participant joined the study, post-interview (between the 19th November 2024 and 13th December 2024).
|
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Burnout score (ProQOL)
Time Frame: The questionnaire was completed at a single time point, depending on when the voluntary participant joined the study, post-interview (between the 19th November 2024 and 13th December 2024).
|
Self-reported scores on the Burnout subscale of the Professional Quality of Life Scale (ProQOL), Version 5 , and questions are scored on a scale of 1 to 5, and raw scores range between 10 to 50. Higher scores indicate higher levels of burnout, representing a less favourable outcome. ProQOL questionnaire, was scored according to the official ProQOL scoring guidelines. The ProQOL is a validated measure with acceptable internal consistency across its subscales, commonly used to assess compassion fatigue and related constructs in healthcare professionals. Descriptive statistics (mean and standard deviation) were calculated. If appropriate, to explore potential sex differences, statistical comparisons were conducted using both Frequentist and Bayesian approaches, with analyses performed in JASP software. |
The questionnaire was completed at a single time point, depending on when the voluntary participant joined the study, post-interview (between the 19th November 2024 and 13th December 2024).
|
|
Secondary Traumatic Stress score (ProQOL)
Time Frame: The questionnaire was completed at a single time point, depending on when the voluntary participant joined the study, post-interview (between the 19th November 2024 and 13th December 2024).
|
Self-reported scores on the Secondary Traumatic Stress subscale of the Professional Quality of Life Scale (ProQOL), Version 5, and questions are scored on a scale of 1 to 5, and raw scores range between 10 to 50. Higher scores indicate greater levels of secondary traumatic stress, representing a less favourable outcome. ProQOL questionnaire, scored according to the official ProQOL scoring guidelines. The ProQOL is a validated measure with acceptable internal consistency across its subscales, commonly used to assess compassion fatigue and related constructs in healthcare professionals. Descriptive statistics (mean and standard deviation) were calculated. If appropriate, to explore potential sex differences, statistical comparisons were conducted using both Frequentist and Bayesian approaches, with analyses performed in JASP software. |
The questionnaire was completed at a single time point, depending on when the voluntary participant joined the study, post-interview (between the 19th November 2024 and 13th December 2024).
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 24118
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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