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Clinical Trials/NCT03068325
NCT03068325
Completed
N/A

Trauma-Focused Equine-Assisted Therapy (TF-EAT) for Veterans With PTSD

Research Foundation for Mental Hygiene, Inc.1 site in 1 country63 target enrollmentApril 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Posttraumatic Stress Disorder
Sponsor
Research Foundation for Mental Hygiene, Inc.
Enrollment
63
Locations
1
Primary Endpoint
Change From Baseline in Clinician-Administered PTSD Scale at 8 Weeks
Status
Completed
Last Updated
last year

Overview

Brief Summary

This study seeks to examine feasibility, acceptability, safety, and preliminary efficacy of Equine-Assisted Therapy for veterans with posttraumatic stress disorder (EAT-PTSD). While several well-studied, validated treatments for PTSD exist, some individuals find these treatments ill-suited, ineffective, or undesirable. EAT is an alternative therapy widely used by organizations, such as PATH International Equine Services, that endorse its effectiveness for treating a variety of mental health issues. These claims have drawn criticism because the published research contains glaring methodological flaws, making it difficult to assess how effective these therapies actually are (Anestis et al., 2014). Equine-assisted therapies present a unique treatment modality that might effectively treat PTSD, particularly for individuals who have difficulty with other treatment modalities. In EAT, a psychotherapist and equine specialist work together to help the patients negotiate interactions with a horse using structured interventions or activities.

Detailed Description

In this pilot study the investigators will develop the EAT intervention and determine whether research methods (evaluation interviews, assessment measures, videotaping procedures) are acceptable to participants. Specifically, the investigators will focus on issues such as session length, appropriateness of the "content" for treatment of PTSD, ordering of session content, adherence to the manual of the equine therapeutic team (based on observations made during supervision and feedback from the consultants), and will detail logistics of data collection and how best to record the sessions (camera angles, etc.).

Registry
clinicaltrials.gov
Start Date
April 2016
End Date
December 2019
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yuval Y Neria

Professor of Medical Psychology

Research Foundation for Mental Hygiene, Inc.

Eligibility Criteria

Inclusion Criteria

  • Between the ages of 18 and 70
  • Current DSM-5 diagnosis of PTSD as determined by a) full criteria met on CAPS, and b) clinical assessment
  • Able to give consent, fluent in English

Exclusion Criteria

  • History of psychiatric diagnosis of psychotic disorder, unstable bipolar disorder
  • Elevated depression of clinical concern and/or score of \>25 on the Hamilton Rating Scale for Depression
  • At elevated risk for suicide based on history and current mental state
  • History of substance/alcohol use disorder at severe level within the past six months, and current diagnosis of substance/alcohol use disorder at a moderate level within past two months
  • Fear of horses or other large animals
  • Orthopedic or other physical conditions and/or limitations that prevent people from walking unassisted and/or walking freely in the ring.

Outcomes

Primary Outcomes

Change From Baseline in Clinician-Administered PTSD Scale at 8 Weeks

Time Frame: 8 weeks

Change in symptoms of PTSD as assessed by the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5, severity rating ranging from 0-80 with higher scores indicating more severe PTSD) in a clinical interview

Study Sites (1)

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