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Completed

NCT Number: NCT03041818

Development of Horse-Riding Program Model for Children With Cerebral Palsy

The purpose of this study is to develop healing riding algorithm applicable in rural riding centers and to apply this to children with cerebral palsy.

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Key information

Age range

5 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

St. Vincent's hospital

Suwon, South Korea

About this study

Horseback riding activities in Korea's riding centers have mostly centered on physical rehabilitation for children with special needs, including those with cerebral palsy, mental disabilities, and autism, with the program conducted by certified equine-assisted therapy instructors. However, there is no definite way to assess the ability of children for horseback riding and no standard riding program. Therefore, developing a assessment and program algorithm for healing horseback riding is expected to contribute to providing more activities for children with special needs and also for general people.

Children older than 4 years old or adolescent with cerebral palsy who voluntarily want to enroll this study would be enrolled.

Participants have 2 times of 30-minute horse riding program for 8 weeks, total 16 times of riding program in a local horse riding center.

Sample size assessment: Calculating for 20% of drop out, 16 patients were calculated to apply the assessment and applicable program.

Drop out: missing more than 2 lessons of horse-riding

Plan for missing data: not included

Statistical analysis plan: paired t-test for the outcome measures

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children or adolescent with cerebral palsy
  • GMFCS level I, II, III
  • Body weight less than 80 kg

Exclusion criteria

  • Medical condition who are not suitable for hippotherapy: severe osteoporosis, mental illness, not controlled seizure disorder etc.
  • Social condition who are not suitable for hippotherapy

Treatment and study plan

Horseback riding therapy

Behavioral

Apply 30 minutes/session, twice a week for 8 weeks of horseback riding therapy (provided with 1 horse rider, 2 side walkers)

Other names: hippotherapy

Primary outcomes

  1. Change of gross motor function (assessment of GMFM-88)

    Time frame: Before the program starts (up to 2 weeks), After the program ends (up to 2 weeks)

    Assessment of GMFM-88 before and after the 16 sessions of horse riding program

  2. Change of Berg balance (assessment of pediatric berg balance scale)

    Time frame: Before the program starts (up to 2 weeks), After the program ends (up to 2 weeks)

    Assessment of pediatric berg balance scale before and after the 16 sessions of horse riding

Secondary outcomes

  1. Actigraph (to monitor activity)

    Time frame: During the horse riding therapy/

    wear an Actigraph to monitor activity of children

  2. Child Health Questionnaire (CHQ)

    Time frame: Before the program starts (up to 2 weeks), After the program ends (up to 2 weeks)

    Caregivers answer the sheets

  3. Postural Assessment Scale for Hippotherapy (PASH)

    Time frame: From starting the therapy, every 2 weeks re-evaluated through study completion, in total 4 times

    Developed tool for assessment of ability for hippotherapy

Sponsors and collaborators

Lead sponsor

The Catholic University of Korea

Other

Collaborators

  • Konkuk University
  • Samsung Medical Center

Registry information

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Feb 3, 2017
Registry last updated
May 18, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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