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Examining the Effectiveness of EAL

Examining the Effectiveness of Equine Assisted Learning for Trauma-exposed Public Safety Personnel

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05579717
Acronym
EAL
Enrollment
40
Registered
2022-10-14
Start date
2022-03-01
Completion date
2025-08-31
Last updated
2025-12-09

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

Conditions

Trauma

Keywords

EAL, PTSD, posttraumatic stress disorder, public safety personnel, first responder, Equine Assisted Learning, horse therapy, trauma

Brief summary

This quasi-experiment will evaluate the effectiveness of Equine Assisted Learning for reducing symptoms associated with trauma exposure among public safety personnel (e.g., fire fighters, police, paramedics, etc.).

Detailed description

The purpose of the proposed project is to investigate the effectiveness of Equine Assisted Learning (EAL) for reducing symptoms associated with trauma exposure among public safety personnel. EAL is an intervention in which mental health clinicians and equine specialists work together with clients to address a learning goal via unmounted interaction with a horse. Recent literature indicates that EAL shows promise in addressing a range of mental health diagnoses among a variety of populations, including military and Royal Canadian Mounted Police veterans with PTSD. The EAL intervention will be delivered at Cartier Farms in Spruce Home, Saskatchewan. Research components of this study will be conducted virtually via Zoom. The investigators will employ a quasi-experimental design with pre-post and follow-up testing. Participants will be assigned one of two groups based on the time that they complete their initial baseline interview: (1) the intervention group will receive the EAL intervention for 8 weeks, while (2) the waitlist control condition will not receive this treatment for the same amount of time. Data on trauma exposure symptom severity will be collected from all participants prior to the start of the the study (baseline), again 8 weeks later (post), and then a final time 3 months later (follow-up). The two conditions will then be compared to determine whether there are differences in trauma exposure symptom severity between groups. To obtain a sufficient sample size while also running appropriately sized interventions of 6-10 participants per session, the researchers will conduct 4-6 rounds of group assignment. All individuals in the waitlist control condition will be offered EAL following their completion of the study.

Interventions

BEHAVIORALEquine Assisted Learning

EAL is an intervention in which mental health clinicians and equine specialists work together with clients to address a learning goal via unmounted interaction with a horse. It is 16 sessions in length, at a rate of two sessions per week.

Sponsors

University of Saskatchewan
CollaboratorOTHER
University of Regina
CollaboratorOTHER
McMaster University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants will be assigned to an intervention group or a waitlist control group based on the time they complete their initial baseline interview. Individuals in the waitlist control group will be offered the opportunity to participate in EAL once they have completed the study.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. English-speaking adults; 2. Currently or previously employed as public safety personnel (e.g., police officer, fire fighter, paramedic, healthcare worker, emergency dispatcher, correctional officer); 3. Reside in Saskatchewan; 4. Meet diagnostic criteria for having experienced a Criterion A traumatic event; 5. Able to provide written informed consent; 6. Have access to a smart phone, tablet, or computer with a working microphone and camera; and 7. Have access to consistent and reliable internet. Exclusion: 1. Meet/met current/past diagnostic criteria for several psychiatric, neurodevelopmental, and neurological conditions; 2. History of severe head trauma with loss of consciousness or history of traumatic brain injury; 3. Have previously completed at least half of the EAL curriculum at Cartier Farms.

Design outcomes

Primary

MeasureTime frameDescription
PTSD symptomatology20 weeksChanges in performance on the Clinician Administered PTSD Scale (structured interview) at pre, post, and follow-up.

Secondary

MeasureTime frameDescription
Emotion regulation20 weeksChanges in performance on the Difficulties in Emotion Regulation Scale, at pre, post, and follow-up. Scores can range between 36 and 180 with higher scores denoting poorer emotion regulation.
Health and disability20 weeksChanges in performance on World Health Organization's Disability Assessment Schedule 12 at pre, post, and follow-up. Scores can range between 0 and 100 with higher scores denoting greater disability.
Disability20 weeksChanges in performance on the Sheehan Disability Scale at pre, post, and follow-up. Scores can range between 0 and 44 with higher scores denoting greater disability.
Work functioning and productivity20 weeksChanges in performance on Lam's Employment and Productivity Scale at pre, post, and follow-up. Scores can range between 0 and 28 with higher scores denoting more severe work impairment.
Mental health symptomatology20 weeksChanges in performance on the Mini International Neuropsychiatric Interview (structured interview) at pre, post, and follow-up.
Depression, anxiety, and stress symptomatology20 weeksChanges in performance on the Depression Anxiety Stress Scale at pre, post, and follow-up. Scores can range between 0 and 42 with higher scores denoting higher depression, anxiety, and/or stress symptomatology.
Substance involvement20 weeksChanges in performance on the World Health Organization's Alcohol, Smoking, and Substance Involvement Test at pre, post, and follow-up. Each question on the ASSIST has a checklist set of responses to choose from to measure substances used in the past, and each response from questions 2 to 7 has a numerical score. Higher scores indicate more significant substance involvement.
Health complaints20 weeksChanges in performance on the Physical Symptoms Questionnaire at pre, post, and follow-up. Scores can range between 0 and 33 with higher scores denoting more health complaints.
Sleep quality20 weeksChanges in performance on the Pittsburgh Sleep Quality Index at pre, post, and follow-up. Scores can range between 0 and 21 with higher scores denoting poorer sleep quality.
Body awareness20 weeksChanges in performance on the Multidimensional Assessment of Interoceptive Awareness - Version 2 at pre, post, and follow-up. Scores can range between 0 and 185 with higher scores denoting greater body awareness.
Moral injury20 weeksChanges in performance on the Moral Injury Assessment - Public Safety Personnel at pre, post, and follow-up. Scores can range between 17 and 102 with higher scores denoting higher moral injury.
Dissociation20 weeksChanges in performance on the Multiscale Dissociation Index at pre, post, and follow-up. Scores can range between 0 and 120 with higher scores denoting higher dissociative symptomatology.
Exposure to childhood traumaCompleted once at baselineBaseline description of trauma experienced in childhood based on the Childhood Trauma Questionnaire, which is a 28-item checklist where more endorsed traumatic experiences indicates more exposure to childhood trauma.
Alcohol use disorder symptomatology20 weeksChanges in performance on the Alcohol Use Disorder Identification Test at pre, post, and follow-up. Scores can range between 0 and 40 with higher scores denoting higher AUD symptomatology.
Cannabis use disorder symptomatology20 weeksChanges in performance on the Cannabis Use Disorder Identification Test at pre, post, and follow-up. Scores can range between 0 and 32 with higher scores denoting higher CUD symptomatology.
Substance use disorder symptomatology20 weeksChanges in performance on the Drug Use Disorder Identification Test at pre, post, and follow-up. Scores can range between 0 and 44 with higher scores denoting higher SUD symptomatology.
Resilience20 weeksChanges in performance on the Brief Resilience Scale at pre, post, and follow-up. Scores can range between 6 and 30 with higher scores denoting higher resilience.
Self-compassion20 weeksChanges in performance on the Self Compassion Scale at pre, post, and follow-up. Scores can range between 26 and 130 with higher scores denoting higher self-compassion.

Other

MeasureTime frameDescription
Experience in EAL8 weeksParticipant experience in EAL as measured by a semi-structured, qualitative interview.
Heart rate variability20 weeksChanges in heart rate variability over time, as measured by a Garmin VivoActive 4 smartwatch.
Sleep quality20 weeksChanges in sleep quality over time, as measured by a Garmin VivoActive 4 smartwatch.

Countries

Canada

Outcome results

None listed

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