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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00717392
Other study ID # SHEBA-08-5327-LG-CTIL
Secondary ID
Status Completed
Phase N/A
First received July 16, 2008
Last updated February 28, 2013
Start date September 2008
Est. completion date July 2012

Study information

Verified date February 2013
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

Hippotherapy is every program of horseback riding meant to treat people with physiological, mental, social, cognitive or behavioral problems. The purpose of the current research is to evaluate the efficacy of hippotherapy for children with developmental disabilities. The hypothesis is that children with developmental disabilities who are treated with hippotherapy will show better outcomes than children with the same problems who are not treated with hippotherapy.


Description:

Hippotherapy is every program of horseback riding meant to treat people with physiological, mental, social, cognitive or behavioral problems. Most studies that tested hippotherapy were uncontrolled and focused on motor problems, such as cerebral palsy. Today, hippotherapy is used for various developmental problems such as Attention deficit / Hyperactivity disorder (ADHD) and Autism spectrum disorder (ASD), without clear information about its efficacy for these populations.

The purpose of the current research is to evaluate the efficacy of 6 months of hippotherapy for children with developmental disabilities. The hypothesis is that children with developmental disabilities who are treated with hippotherapy for 6 months will show better outcomes than children with the same problems who are not treated with hippotherapy.

Assessment:

- BRIEF questionnaire

- Stony Brook Questionnaire

All questionnaires will be applied at the beginning of the study and after 6 months.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date July 2012
Est. primary completion date June 2011
Accepts healthy volunteers No
Gender Both
Age group 5 Years to 17 Years
Eligibility Inclusion Criteria:

- Age: 5-17 years.

- A diagnosis of ADHD or ASD.

Exclusion Criteria:

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Weinberg Child Development Center, Sheba Medical Center, Tel-Hashomer Ramat-Gan

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improving the parameters of autism Repetitive behaviors Eye contact Communication Repetitive behaviors No
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