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临床试验/NCT05579717
NCT05579717已完成不适用

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

McMaster University2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2022年3月1日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
2
主要终点
PTSD symptomatology

研究概览

简要总结

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.).

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

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

排除标准

  • 未提供

结局指标

主要结局

PTSD symptomatology

时间窗: 20 weeks

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

次要结局

  • Mental health symptomatology(20 weeks)
  • Depression, anxiety, and stress symptomatology(20 weeks)
  • Substance involvement(20 weeks)
  • Health complaints(20 weeks)
  • Sleep quality(20 weeks)
  • Body awareness(20 weeks)
  • Moral injury(20 weeks)
  • Dissociation(20 weeks)
  • Emotion regulation(20 weeks)
  • Exposure to childhood trauma(Completed once at baseline)
  • Alcohol use disorder symptomatology(20 weeks)
  • Cannabis use disorder symptomatology(20 weeks)
  • Substance use disorder symptomatology(20 weeks)
  • Resilience(20 weeks)
  • Self-compassion(20 weeks)
  • Health and disability(20 weeks)
  • Disability(20 weeks)
  • Work functioning and productivity(20 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Margaret McKinnon

Professor

McMaster University

研究点 (2)

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