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Clinical Trials/NCT05869253
NCT05869253
Completed
N/A

The Efficacy of Attention Skill Therapy (ASTride), an Equine Assisted Occupational Therapy Intervention, for Children With Attention Deficit Hyperactivity Disorder (ADHD) on Cognitive-emotional Aspects, Daily Function and Participation

Tel Aviv University1 site in 1 country50 target enrollmentFebruary 1, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Attention-deficit Hyperactivity Disorder
Sponsor
Tel Aviv University
Enrollment
50
Locations
1
Primary Endpoint
The Behavior Rating Inventory of Executive Function (BRIEF) (Gioia, Isquith, Guy, & Kenworthy, 2000)
Status
Completed
Last Updated
7 months ago

Overview

Brief Summary

The goal of this clinical trial is to develop and validate an Equine Assisted Occupational Therapy Intervention for children aged 6-12 with Attention Deficit Hyperactivity Disorder.

The research aims to study the effect of an EAOT intervention on cognitive-emotional aspects, daily function and participation among these children using various measurements including physiological measures (EEG, heart rate for rider and horse), questionnaires and different tasks. It aims to enable the creation of an evidence based protocol for professionals in order to provide a better suited therapy for children with ADHD and enable them to live a full life. Participants will enroll in a 12 week EAOT intervention including one session per week of 45 minutes with a waiting period prior the intervention. Participants will go through assessments prior waiting time, prior the intervention and post intervention.

Detailed Description

Introduction: Attention deficit/hyperactivity disorder (ADHD), characterized by inattention, hyperactivity and impulsivity, is currently one of the most common diagnoses given to children. ADHD is characterized by a developmental and chronic impairment, Executive Functions (EFs), cognitive-emotional and sensory-motor functions, as well as a wide variety of difficulties in daily tasks beyond the core symptoms. Literature review indicated that current intervention protocols include pharmacological treatment and address specific aspects such as behavioral or psychological, though scarce interventions address both. Objectives: The purpose of this study is to examine the feasibility of conducting an Equine Assisted Occupational Therapy (EAOT) intervention for children with ADHD aiming to improve EFs, cognitive-emotional functions and participation. Method: A prospective cohort study with Interrupted Time-Series design will be conducted. Forty participants and their parents who were referred to EAOT will be recruited from the waiting list of Harey Yehuda stables. Assessments will take place at four time points. Time 1: baseline-when referred for EAOT. Time 2: pre-test, before first treatment session, end of 12 week waiting period. Time 3: post-test after 12 weeks of intervention and time 4: post intervention assessment, three months follow up. The intervention will be administered by a licensed EAOT, and assessments will be done by a blinded licensed occupational therapist (OT). Standardized assessment measures will be used to measure EFs, cognitive-emotional and sensory-motor aspects as well as participation at each time point.

Registry
clinicaltrials.gov
Start Date
February 1, 2023
End Date
February 1, 2025
Last Updated
7 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Orit Bart PhD

Lead investigator

Tel Aviv University

Eligibility Criteria

Inclusion Criteria

  • Children between 6 and 12 years of age
  • Diagnosis of ADHD from a medical professional based on DSM-5 criteria with or without medication (e.g., psychostimulant medication)
  • General doctors' approval and referral for participating in EAS

Exclusion Criteria

  • Moderate to severe cognitive impairment
  • Neurological disorders (e.g., epilepsy)
  • Children with additional developmental disorders (e.g., Autism, Cerebral Palsy)
  • Children who will begin new medicine treatment or change existing treatment during intervention
  • Children with severe sensory loss (e.g., blindness).

Outcomes

Primary Outcomes

The Behavior Rating Inventory of Executive Function (BRIEF) (Gioia, Isquith, Guy, & Kenworthy, 2000)

Time Frame: 3 months

standardized ecological rating scale filled by a parent, designed to reflect the neuropsychological constructs of EF in everyday situations for children aged 5-18

Secondary Outcomes

  • The Screen for Child Anxiety Related Emotional Disorders (SCARED)(3 months)
  • Canadian Occupational Performance Measure (COPM) (Law et al., 2014)(3 months)
  • The children Participation Questionnaire (CPQ)(3 months)
  • The new General Self-efficacy Scale (NGSE)(3 months)
  • The Brain Engagement Index; BEI (Shahaf et al., 2018)(3 months)
  • The Hebrew adaptation of The Children's Hope Scale (Snyder, 2002)(3 months)
  • The Short Sensory Profile (SSP)(3 months)
  • the Tower of Hanoi test (Lezak et al., 2004).(3 months)
  • The Bruininks-Oseretsky Test of Motor Proficiency, Second Edition (BOT-2)(3 months)
  • The Child Performance Skill Questionnaire (PSQ)(3 months)

Study Sites (1)

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