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Horse Therapy for PTSD (EAL Trial)
EAL Trial Summary
This trial will test if horse therapy helps public safety workers reduce PTSD symptoms. #mentalhealth #therapy #horsetherapy
EAL Trial Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.EAL Trial Design
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Who is running the clinical trial?
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- My substance use does not interfere with my participation in treatments.I have been diagnosed with PTSD.
- Group 1: Equine Assisted Learning group
- Group 2: Waitlist control group
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Are there any available slots for participants in this research trial?
"Indeed, the records on clinicaltrials.gov reveal that this medical trial is actively recruiting participants which was initially published on March 1st 2022 and subsequently revised for accuracy on March 13th 2023. The total number of individuals needed amounts to 80 from a single institution."
How many participants are being included in this investigation?
"Affirmative. Data found on clinicaltrials.gov confirms that this study, which was initially advertised on March 1st 2022, is currently soliciting participants. Approximately 80 volunteers need to be enrolled from one medical centre."
What is the ultimate goal of this research project?
"This 20-week trial aims to observe changes in emotional regulation, resilience (as measured by Brief Resilience Scale scores 6-30), health and disability as judged by the World Health Organization's Disability Assessment Schedule 12 0-100) and heart rate variability using a Garmin VivoActive 4 smartwatch."
Who else is applying?
What site did they apply to?
What portion of applicants met pre-screening criteria?
Why did patients apply to this trial?
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