- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02891421
Therapeutic Horsemanship in Veterans
Effects of Equine Assisted Activities on PTSD Symptoms, Coping Self-efficacy, Emotion Regulation, and Social Engagement in U.S. Military Veterans
Study Overview
Status
Intervention / Treatment
Detailed Description
Large numbers of post-deployed U.S. veterans diagnosed with Post Traumatic Stress Disorder (PTSD) and/or Traumatic Brain Injury make effective interventions urgent, to reduce symptoms and increase veterans' coping. PTSD includes anxiety, flashbacks, and emotional numbing. Symptoms expand health care costs for stress-related illnesses making veterans' civilian life difficult.
The proposed study used a randomized experimental design with repeated measures and waitlist control group testing the efficacy of a 6-week human-horse interaction and systematic therapeutic horseback riding program in: decreasing PTSD symptoms, increasing coping self efficacy, emotion regulation, and social engagement. The Riding Group spent one hour weekly interacting with and riding the same horse at one of two PATH-accredited riding centers in Mid-Missouri supervised by an Occupational Therapist, Profession Association of Therapeutic Horsemanship (PATH) International-certified instructor, leader and side walkers as needed. Riding was directed by a systematic lesson plan. Data collection occured at baseline, 3 weeks, and 6 weeks. The Control Group was assessed at the same intervals and again 3 weeks and 6 weeks after joining the Riding Group.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age 18 years or older
- Veterans, left active military service (not serving in reserve units.)
- Diagnosed with Post Traumatic Stress Disorder/Traumatic Brain Injury or both according to ICD-9 diagnostic codes.
- Weight less than 220 pounds.
- Able to walk at least 25 feet without the assistance of a person (but potentially with assistive devices).
- Willing to interact with and ride a horse.
- Have not ridden a horse in the past year.
- Care Provider assent
Exclusion Criteria:
- Age less than 18 years
- Veterans in active military service (including reserve units).
- No diagnosis of PTSD/TBI or both according to ICD-9 diagnostic codes.
- Weight greater than 221 pounds.
- Unable to walk at least 25 feet without the assistance of a person (but potentially with assistive devices.)
- Unwilling to interact with and ride a horse.
- Have been riding a horse in the past year.
- Care Provider unwilling to provide assent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Therapeutic Horseback Riding
Therapeutic Horseback Riding: Veterans were matched to a horse by the instructor and occupational therapist for best fit and the same horse was ridden each week
|
Veterans were matched to a horse for best fit and the same horse was ridden each week.
The warm-up exercises involved various repeated physical movements while the horse was walking or standing steady, such as head rotations, lifting arms, rotating ankles, flexing toes.
The exercises began with riding at a walk during the early weeks, learning reining skills and riding positions, and progressed to light trotting.
Veteran participants were able to build on skill sets related to grooming, tacking, mounting, and riding that were introduced in prior weeks.
Skill progression was based on individual abilities and safety as determined by certified riding instructor and occupational therapist.
|
Other: Standard Care
Participants received standard care.
|
Standard Care: Participants received standard care
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Coping Self-Efficacy Scale (CSES)
Time Frame: Day 1, 3 weeks and 6 weeks
|
26 item, 11 point analog scale
|
Day 1, 3 weeks and 6 weeks
|
Change in Post-Traumatic Stress Disorder Checklist-Military Version (PCL-M)
Time Frame: Day 1, 3 weeks and 6 weeks
|
17 item, 5 point scale
|
Day 1, 3 weeks and 6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Social and Emotional Loneliness Scale for Adults (SELSA) scale
Time Frame: Day 1, 3 weeks and 6 weeks
|
15 item, 7 point Likert-type scale.
|
Day 1, 3 weeks and 6 weeks
|
Change in Difficulties in Emotion Regulation Scale (DERS)
Time Frame: Day 1, 3 weeks and 6 weeks
|
36 item, 5 point Likert-type scale
|
Day 1, 3 weeks and 6 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Rebecca A Johnson, PhD, University of Missouri-Columbia
Publications and helpful links
General Publications
- Bisson J, Andrew M. Psychological treatment of post-traumatic stress disorder (PTSD). Cochrane Database Syst Rev. 2007 Jul 18;(3):CD003388. doi: 10.1002/14651858.CD003388.pub3.
- Hoge CW, McGurk D, Thomas JL, Cox AL, Engel CC, Castro CA. Mild traumatic brain injury in U.S. Soldiers returning from Iraq. N Engl J Med. 2008 Jan 31;358(5):453-63. doi: 10.1056/NEJMoa072972. Epub 2008 Jan 30.
- Brewin CR, Andrews B, Valentine JD. Meta-analysis of risk factors for posttraumatic stress disorder in trauma-exposed adults. J Consult Clin Psychol. 2000 Oct;68(5):748-66. doi: 10.1037//0022-006x.68.5.748.
- Hakanson M, Moller M, Lindstrom I, Mattsson B. The horse as the healer-a study of riding in patients with back pain. J Bodyw Mov Ther. 2009 Jan;13(1):43-52. doi: 10.1016/j.jbmt.2007.06.002. Epub 2007 Aug 24.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1207664-1
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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