Investigation of Equine Assisted Therapy for Post-Traumatic Stress Disorder

Sponsor
Western University, Canada (Other)
Overall Status
Recruiting
CT.gov ID
NCT02816788
Collaborator
(none)
26
1
1
78.3
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Study Details

Study Description

Brief Summary

In partnership with SARI Therapeutic Riding (SARI TR) and other equine therapy locations, Brescia University College, at the University of Western Ontario, will study the use of Equine Assisted Therapy (EAT) for military veterans and "first reponders" (emergency services personell) diagnosed with Post-Traumatic Stress Disorder. Data will be collected through tests and questionnaires, and follow-up interviews with participants. It is expected that after a series of EAT sessions, the social, emotional and psychological well-being of participants will be improved and PTSD symptoms alleviated.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Equine Assisted Therapy (EAT)
N/A

Detailed Description

The objective of this study is to evaluate outcomes of participation in Equine Assisted Therapy for those with a history of PTSD.

This study protocol will be a within subjects design: Treatment group with pre- and post-intervention comparisons. Participants will be Military Veterans and "first responders" (emergency services personell) with prior diagnosis of PTSD; N=8 to 10.

Procedures for treatment group: The treatment group will engage in sets of EAT sessions to be run at SARI Therapeutic Riding (SARI TR) and other equine therapy locations. A typical EAT session will involve beginning the session by checking in as a group, engaging in one or two activities with the horses and then processing the activity as a group. Each session will also end with a check out. The activities with equines will range from observation/educational, grooming, reflective work involving creative expression with writing/art, or more active activities such as leading. Each session will have an overall topic which will provide the framework for the session. Interactions with equines will take place in the indoor arena (an enclosed space for riding/training horses), whilst other aspects of the sessions will take place in the main lounge. Sessions will be conducted by a Clinical Counsellor certified with their Provincial Counselling and Psychotherapy Association, assisted by other certified personnel, including those with horse handling experience. Each session will include up to eight to ten participants. There will be two persons with therapeutic expertise and one with horse/TR experience attending to participants at all times during interaction with equines. Sessions will usually last about two and a half hours, incorporating psychotherapy and interacting with equines, over a course of several sessions.

General procedure: Military Veterans and first responders with PTSD will be recruited from the local Occupational Stress Injury Social Support (OSISS) PTSD support group and similar organizations. This service "is a partnership program between the Department of National Defence and Veterans Affairs Canada" (OSISS website) created to provide peer support to Canadian Forces personnel, Veterans and their families. The OSISS provides peer support and aids in linking members to appropriate services, programmes and supports. Data will be collected through questionnaire-type tests and post-session interview of participants. A set of short tests, the Rosenberg Self-esteem Scale, the Positive and Negative Affect Scale (PNAS), and the PTSD Checklist for DSM-5 (PCL-5) will be administered. Participants will complete sets of tests at pre-session, post-session, and follow-up, and will be interviewed one week after the end of the study in order to obtain further data. Longer-term follow-up is also anticipated, with measures being repeated at further time points (e.g., one-, three-, and six-month follow-up) after completion of EAT sessions.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
26 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Single group, within subjects comparison. Pre- and post-intervention comparisons.Single group, within subjects comparison. Pre- and post-intervention comparisons.
Masking:
None (Open Label)
Masking Description:
No masking.
Primary Purpose:
Treatment
Official Title:
Investigation of Equine Assisted Therapy for Post-Traumatic Stress Disorder
Actual Study Start Date :
Jun 20, 2017
Anticipated Primary Completion Date :
Aug 30, 2023
Anticipated Study Completion Date :
Dec 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Equine Assisted Therapy (EAT)

Equine Assisted Therapy (EAT) treatment group

Behavioral: Equine Assisted Therapy (EAT)
Psychotherapy incorporating use of equines (Equine Assisted Therapy; EAT) to facilitate therapy to improve the social, emotional and psychological well-being of participants and alleviate PTSD symptoms.

Outcome Measures

Primary Outcome Measures

  1. Understanding of effects/effectiveness of EAT for PTSD. [6 months]

    PTSD Checklist for Diagnostic and Statistical Manual-5 (PCL-5)

Secondary Outcome Measures

  1. Understanding of effects/effectiveness of EAT for PTSD-related moods and emotions. [6 months]

    Positive and Negative Affect Scale (PNAS)

  2. Understanding of effects/effectiveness of EAT for PTSD-related self esteem issues. [6 months]

    Rosenberg Self Esteem Scale

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Diagnosis of Post-Traumatic Stress Disorder (PTSD)

  • with veteran or "first responder" status

  • Both of these ascertained by self-report, confirmed by membership in Occupational Stress Injury Social Support (OSISS) group or similar organization

Exclusion Criteria:
  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 Western University London Ontario Canada N6A 3K7

Sponsors and Collaborators

  • Western University, Canada

Investigators

  • Principal Investigator: Anne MC Barnfield, PhD, Western University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Anne Barnfield, Dr., Western University, Canada
ClinicalTrials.gov Identifier:
NCT02816788
Other Study ID Numbers:
  • 108102
First Posted:
Jun 29, 2016
Last Update Posted:
Aug 23, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Anne Barnfield, Dr., Western University, Canada
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 23, 2022