The Therapeutic Effects of Equine-Assisted Psychotherapy (EAP)

March 2, 2021 updated by: Chua Yi Rong Shawn

The Therapeutic Effects of Equine-Assisted Psychotherapy on Lowering Aggression Levels Through an Increase of Emotion Regulation

Equine-assisted interventions (EAI) are an emerging form of alternate psychotherapy that has been increasingly found to produce improvements in various treatment outcomes. However, the paucity of randomized-controlled trials (RCTs) in the EAI literature prevents any definitive conclusions to be made about the general effectiveness of EAI. This study tests whether one form of EAI, Equine-Assisted Psychotherapy (EAP), reduces aggression and alters risk factors associated with aggression in young adults, and whether emotion regulation mediates any effect of EAP on aggression. In a single-blind RCT, undergraduate students will be randomly assigned to either an intervention group, an active-control group, or a placebo-control group. Participants in the intervention group will undergo a 5-week EAP program consisting of structured, interactive activities with horses followed by a clinical processing component. Participants in the active control group will undergo a 5-week program that only involves interactions with horses without any clinical input (i.e. commonly coined as animal-assisted activities). Participants in the placebo-control group will undergo 5 weeks of 1-hour movie sessions related to horses. There will be three waves of data collection measuring key outcome variables - t1 before the 1st session, t2 after the 3rd session, and t3 after the final session. Participants will complete questionnaires assessing the key outcomes of aggression, emotional well-being and academic performance. Other risk factors of antisocial behaviour such as psychopathy, level of empathy, emotion regulation and executive functioning will also be measured. To the author's knowledge, the current study is the first in Singapore to investigate if EAP can lower aggression levels and alter psychological risk factors for aggression in healthy young adults. In turn, these results could help inform the utility and validity of EAP in the forensic populations.

Study Overview

Detailed Description

The EAP program will span over the duration of 5 weeks, each week having a 1-hour session. 50 minutes will be allocated to interacting with the horses and the activities while the remaining 10 minutes will be allocated to the clinical processing of the behavior, thoughts and emotions that are observed during the session. This processing will be guided by trained therapists who hold the relevant qualifications (i.e. equine-assisted psychotherapy certification). 2 horses (an Oldenburg and a pony, aged 19 and 14 respectively), 2 therapists, and 2 experienced horse handlers will be present throughout the sessions. Each 1-hour session will consist a maximum of 8 participants that will be split into two groups of 4 such that 1 horse, 1 therapist and 1 experienced horse handler are attached to them.

The design of the experiment will be a single-blind Randomized Controlled Trial. Participants will be told that this study aims to investigate the therapeutic effects of two different EAP programs (either watching video clips related to horses or actual interactions with horses) and that they will be randomly assigned to either one. In actuality, participants are randomly assigned to either an intervention group, an active-control group or a placebo-control group. 3 time points of data collection are measured throughout the 5-week duration - t1 before the 1st session, t2 after the 3rd session, and t3 after the final session. All participants will go through the same questionnaire administered at each time point during the 5-week duration regardless of their assigned group. Participants in the intervention group will go through the 5-week EAP program consisting of the clinical processing following some activities found in EAP manuals. Participants in the active-control group will undergo a 5-week program that only involves interactions with horses without any clinical input (i.e. commonly coined as animal-assisted activities). Participants in the placebo-control group will undergo a 5-week movie screening of 1 hour each session that is related to horses in the lab.

Participant recruitment will begin as soon as possible once approval has been given and should not take longer than 2 weeks to recruit a total of 120 undergraduate students from both NUS and NTU.

The 5-week intervention program will be briefly structured as such:

Session 1: Introduction to grooming and horse safety This introductory session is aimed at getting participants to be familiar with the safety features when working with these horses as well as to be attentive to the warning cues that horses display that is indicative of their mood. Once that has been briefed, participants will be taught how to groom the horse as part of learning natural horsemanship skills. These includes brushing and cleaning the hooves of the horse.

Session 2: Review of grooming, learning to put on halter and leading the horse The second session is built upon the previous session in that reviews of grooming and horse safety will continually be surfaced throughout the program as such lessons is always an ongoing process. On top of that, participants will be taught how to put on a halter on the horse and to lead the horse. The session ends with a modified activity called Catch and Release which allows participants to have personal interaction with the horse.

Session 3: Review of grooming and Give-and-Take The third session is more focused on the importance of proper communication as this helps convey the investigators intentions across with greater accuracy while still remaining respectful and mindful of the other party on the receiving end. After the grooming segment, participants will engage in an activity called Give-and-Take which work improving communication in a non-verbal manner only through the string they are provided with to guide the horse.

Session 4: Review on grooming and Life's Little Obstacles This session is aimed at utilizing participants' critical thinking skills to achieve the objective of the activity. This is meant to push participants' out of their comfort zones which could bring about feelings of frustration and worry that can be processed after the activity is over. The activity that is meant to create such a roadblock is the Life's Little Obstacles whereby participants are told to make the horse jump over a low obstacle with multiple restrictions.

Session 5: Review on grooming, Equine Billiards, and closing This final session is aimed at utilizing participants' problem-solving skills through the use of non-verbal communication. This is done using the Equine Billiards activity whereby the lessons learnt from previous sessions would culminate in this one task. Following the processing of the activity after it ends, the therapy team and participants would gather in a circle for the program closure to integrate whatever they have learnt from the past 5-weeks.

GPower 3.1 was used to calculate an appropriate sample size for a medium effect size of 0.15, power at 0.95 and alpha error probability at 0.05. For a multiple linear regression analysis with 2 tested predictors and total number of 4 predictors, the calculation yielded a total sample size of 119. This number was rounded up to 120.

All data will be analyzed using SPSS version 22. Some potential analyses include multiple linear regression, ANCOVAs and their respective post-hoc t-tests, paired-sample t-tests to demonstrate significant changes between pre and post intervention groups, and PROCESS Macro for the mediator analysis.

Study Type

Interventional

Enrollment (Actual)

102

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Singapore, Singapore, 286965
        • Therapeutic and Educational Riding in Singapore

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 28 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Do not have any medical allergies or discomfort from interaction with horses.

Exclusion Criteria:

  • Participants who self-report an existing diagnosis for a psychological disorder as defined by the Diagnostic and Statistical Manual of Mental Disorders, 5th edition: DSM-V

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: OTHER
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Intervention Group
Participants in the intervention group will go through the 5-week EAP program consisting of the clinical processing following some activities found in EAP manuals.
Equine-Assisted Psychotherapy (EAP) involves working on the psychological goals set between the client and the mental health professional. This is done through the experiential interactions between the clients and the horse. This experiential aspect is vital as it allows clients to process the emotions, thoughts and behaviors that were expressed during sessions with the horse.
Other Names:
  • Equine-Facilitated Psychotherapy
Simple interactions with the horses that does not necessarily involve any goals being set between the client and the personnel handling the session. These can involve activities such as grooming or petting of the horse.
ACTIVE_COMPARATOR: Active-control group
Participants in the active-control group will undergo a 5-week program that only involves interactions with horses without any clinical input (i.e. commonly coined as animal-assisted activities).
Simple interactions with the horses that does not necessarily involve any goals being set between the client and the personnel handling the session. These can involve activities such as grooming or petting of the horse.
PLACEBO_COMPARATOR: Placebo-control group
Participants in the placebo-control group will undergo a 5-week movie screening of 1 hour each session that is related to horses.
This group will only be watching movies related to horses and they are told that this is another form of EAP even though this is not the case. This type of intervention has not been known to provide any therapeutic effect relevant to the study and thus is used as the placebo-control.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Young Adult Behavioral Scale (YABS)
Time Frame: Immediately before the 1st intervention session
Min. Value: 1 (never), Max. Value: 5 (always), higher scores indicate a higher likelihood in the domains of relational aggression, social aggression and interpersonal maturity.
Immediately before the 1st intervention session
Young Adult Behavioral Scale (YABS)
Time Frame: Immediately after the 3rd intervention session
Min. Value: 1 (never), Max. Value: 5 (always), higher scores indicate a higher likelihood in the domains of relational aggression, social aggression and interpersonal maturity.
Immediately after the 3rd intervention session
Young Adult Behavioral Scale (YABS)
Time Frame: Immediately after the 5th intervention session
Min. Value: 1 (never), Max. Value: 5 (always), higher scores indicate a higher likelihood in the domains of relational aggression, social aggression and interpersonal maturity.
Immediately after the 5th intervention session
Reactive-Proactive Aggression Questionnaire (RPQ)
Time Frame: Immediately before the 1st intervention session
Min. Value: 0 (never), Max. Value: 2 (often), higher scores indicate higher general aggression levels
Immediately before the 1st intervention session
Reactive-Proactive Aggression Questionnaire (RPQ)
Time Frame: Immediately after the 3rd intervention session
Min. Value: 0 (never), Max. Value: 2 (often), higher scores indicate higher general aggression levels
Immediately after the 3rd intervention session
Reactive-Proactive Aggression Questionnaire (RPQ)
Time Frame: Immediately after the 5th intervention session
Min. Value: 0 (never), Max. Value: 2 (often), higher scores indicate higher general aggression levels
Immediately after the 5th intervention session
Depression Anxiety Stress Scale - 21 items (DASS-21)
Time Frame: Immediately before the 1st intervention session
Min. Value: 0 (did not apply to me at all), Max. Value: 3 (applied to me very much, or most of the time), higher scores indicate poorer emotional well-being
Immediately before the 1st intervention session
Depression Anxiety Stress Scale - 21 items (DASS-21)
Time Frame: Immediately after the 3rd intervention session
Min. Value: 0 (did not apply to me at all), Max. Value: 3 (applied to me very much, or most of the time), higher scores indicate poorer emotional well-being
Immediately after the 3rd intervention session
Depression Anxiety Stress Scale - 21 items (DASS-21)
Time Frame: Immediately after the 5th intervention session
Min. Value: 0 (did not apply to me at all), Max. Value: 3 (applied to me very much, or most of the time), higher scores indicate poorer emotional well-being
Immediately after the 5th intervention session
Motivated strategies for Learning Questionnaire (MSLQ)
Time Frame: Immediately before the 1st intervention session
Min. Value: 1 (not at all true of me), Max. Value: 7 (very true of me), higher scores indicate greater motivations to learn using the different strategies
Immediately before the 1st intervention session
Motivated strategies for Learning Questionnaire (MSLQ)
Time Frame: Immediately after the 3rd intervention session
Min. Value: 1 (not at all true of me), Max. Value: 7 (very true of me), higher scores indicate greater motivations to learn using the different strategies
Immediately after the 3rd intervention session
Motivated strategies for Learning Questionnaire (MSLQ)
Time Frame: Immediately after the 5th intervention session
Min. Value: 1 (not at all true of me), Max. Value: 7 (very true of me), higher scores indicate greater motivations to learn using the different strategies
Immediately after the 5th intervention session
Emotion Regulation Questionnaire (ERQ)
Time Frame: Immediately before the 1st intervention session
Min. Value: 1 (strongly disagree), Max. Value: 7 (strongly agree), higher scores indicate greater likelihood of using the two types of emotion regulation strategies
Immediately before the 1st intervention session
Emotion Regulation Questionnaire (ERQ)
Time Frame: Immediately after the 3rd intervention session
Min. Value: 1 (strongly disagree), Max. Value: 7 (strongly agree), higher scores indicate greater likelihood of using the two types of emotion regulation strategies
Immediately after the 3rd intervention session
Emotion Regulation Questionnaire (ERQ)
Time Frame: Immediately after the 5th intervention session
Min. Value: 1 (strongly disagree), Max. Value: 7 (strongly agree), higher scores indicate greater likelihood of using the two types of emotion regulation strategies
Immediately after the 5th intervention session
Difficulties in Emotion Regulation Scale - Short Form (DERS-SF)
Time Frame: Immediately before the 1st intervention session
Min. Value: 1 (almost never), Max. Value: 5 (almost always), higher scores indicate greater difficulties with emotion regulation
Immediately before the 1st intervention session
Difficulties in Emotion Regulation Scale - Short Form (DERS-SF)
Time Frame: Immediately after the 3rd intervention session
Min. Value: 1 (almost never), Max. Value: 5 (almost always), higher scores indicate greater difficulties with emotion regulation
Immediately after the 3rd intervention session
Difficulties in Emotion Regulation Scale - Short Form (DERS-SF)
Time Frame: Immediately after the 5th intervention session
Min. Value: 1 (almost never), Max. Value: 5 (almost always), higher scores indicate greater difficulties with emotion regulation
Immediately after the 5th intervention session

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-Report Psychotherapy - Short Form (SRP-SF)
Time Frame: Immediately before the 1st intervention session
Min. Value: 1 (strongly disagree), Max. Value: 5 (strongly agree), higher scores indicate higher levels of psychopathy
Immediately before the 1st intervention session
Self-Report Psychotherapy - Short Form (SRP-SF)
Time Frame: Immediately after the 3rd intervention session
Min. Value: 1 (strongly disagree), Max. Value: 5 (strongly agree), higher scores indicate higher levels of psychopathy
Immediately after the 3rd intervention session
Self-Report Psychotherapy - Short Form (SRP-SF)
Time Frame: Immediately after the 5th intervention session
Min. Value: 1 (strongly disagree), Max. Value: 5 (strongly agree), higher scores indicate higher levels of psychopathy
Immediately after the 5th intervention session
Cognitive, Affective and Somatic Empathy Scales (CASES)
Time Frame: Immediately before the 1st intervention session
Min. Value: 0 (rarely), Max. Value: 2 (often), higher scores indicate higher levels of empathy
Immediately before the 1st intervention session
Cognitive, Affective and Somatic Empathy Scales (CASES)
Time Frame: Immediately after the 3rd intervention session
Min. Value: 0 (rarely), Max. Value: 2 (often), higher scores indicate higher levels of empathy
Immediately after the 3rd intervention session
Cognitive, Affective and Somatic Empathy Scales (CASES)
Time Frame: Immediately after the 5th intervention session
Min. Value: 0 (rarely), Max. Value: 2 (often), higher scores indicate higher levels of empathy
Immediately after the 5th intervention session
Trail Making Task - Part B (TMT - Part B)
Time Frame: Immediately before the 1st intervention session
Unit of measure: Reaction Time (s), higher scores indicate higher levels of executive functioning, more specific to attention span and attentional task switching abilities
Immediately before the 1st intervention session
Trail Making Task - Part B (TMT - Part B)
Time Frame: Immediately after the 3rd intervention session
Unit of measure: Reaction Time (s), higher scores indicate higher levels of executive functioning, more specific to attention span and attentional task switching abilities
Immediately after the 3rd intervention session
Trail Making Task - Part B (TMT - Part B)
Time Frame: Immediately after the 5th intervention session
Unit of measure: Reaction Time (s), higher scores indicate higher levels of executive functioning, more specific to attention span and attentional task switching abilities
Immediately after the 5th intervention session

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Lim SM Matthew, PhD, PsyD, National University, Singapore

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 20, 2020

Primary Completion (ACTUAL)

April 9, 2020

Study Completion (ACTUAL)

November 6, 2020

Study Registration Dates

First Submitted

December 11, 2019

First Submitted That Met QC Criteria

December 13, 2019

First Posted (ACTUAL)

December 16, 2019

Study Record Updates

Last Update Posted (ACTUAL)

March 3, 2021

Last Update Submitted That Met QC Criteria

March 2, 2021

Last Verified

March 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

There is no plans for such sharing as of now.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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