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NCT Number: NCT07739680

EFFECTS OF HIPPOTHERAPY IN CHILDREN WITH CEREBRAL PALSY

Cerebral palsy is a group of permanent disorders affecting movement and posture due to non-progressive disturbances in the developing brain. The aim of this study is to investigate the effects of hippotherapy on physical function, including balance, trunk control, posture, and handgrip strength, as well as bladder and bowel symptoms and family quality of life in children with cerebral palsy.

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Key information

Age range

7 year–15 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ankara Yildirim Beyazit University

Ankara, Turkey (Türkiye)

Location contact

Elif Sena Dusgun, PhD

SUB_INVESTIGATOR

General Secretariat

CONTACT

[email protected]

+90 312 906 2000

Rumeysa Karayel, BSc

SUB_INVESTIGATOR

Seyda Toprak Celenay, PhD

PRINCIPAL_INVESTIGATOR

Tugba Kilickaya, BSc

SUB_INVESTIGATOR

About this study

Cerebral palsy is a group of permanent disorders of movement and posture caused by non-progressive disturbances in the developing brain. Children with cerebral palsy may experience limitations in balance, trunk control, posture, mobility, and daily activities.

During hippotherapy, the rhythmic and multidirectional movements of the horse provide continuous sensory and motor stimulation, requiring the child to make repeated postural adjustments. These characteristics may support balance, postural control, muscle activation, and functional performance.

Although the effects of hippotherapy on motor function in children with cerebral palsy have been investigated, evidence regarding its combined effects on physical function, bladder and bowel symptoms, and family quality of life remains limited. Therefore, the present study aims to investigate the effects of hippotherapy on physical function-including balance, trunk control, posture, and handgrip strength-as well as bladder and bowel symptoms and family quality of life in children with cerebral palsy. The findings may contribute to the literature and provide guidance for rehabilitation practices.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Being between 7 and 15 years of age, Having a diagnosis of cerebral palsy confirmed by a specialist physician, Having a Gross Motor Function Classification System (GMFCS) level between I and III, Being able to understand and follow basic verbal commands, Being able to stand independently for at least 30 seconds, Having no medical contraindications to participation in hippotherapy, Volunteering to participate in the study and providing written informed consent from a parent or legal representative.

Exclusion criteria

Presence of an active infection, Bladder and bowel symptoms caused by an organic condition, such as Hirschsprung disease or anorectal malformation, Having received hippotherapy within the previous 12 months, Having uncontrolled epilepsy or having experienced a seizure within the previous 6 months, Being unable to comply with the assessment or treatment program because of severe behavioral problems, Being unable to attend the treatment program regularly, Having undergone surgery affecting the spine, pelvis, or lower extremities within the previous 12 months, Presence of severe hip dislocation, atlantoaxial instability, uncontrolled scoliosis, or other orthopedic conditions that constitute a contraindication to hippotherapy.

Treatment and study plan

Hippotherapy Program

Other

Participants will receive 30-minute hippotherapy sessions once weekly for 8 weeks in addition to their ongoing special education program. The program will include exercises targeting balance, postural control, trunk stabilization, coordination, muscle strength, upper extremity function, and sensory processing.

Special Education Program

Other

Participants will continue their ongoing special education program throughout the 8-week study period. The program includes educational activities, speech and language therapy, occupational therapy, proprioceptive activities, and sensory-based interventions according to the individual needs of the child.

Primary outcomes

  1. Balance

    Time frame: Baseline and at the end of the 8-week intervention

    Balance will be assessed using the Pediatric Balance Scale, a 14-item scale evaluating sitting balance, standing balance, transfers, reaching, turning, and stepping activities. The total score ranges from 0 to 56, with higher scores indicating better balance performance. The scale will be administered by a physiotherapist.

  2. Trunk Control

    Time frame: Baseline and at the end of the 8-week intervention

    Trunk control will be assessed using the Trunk Control Measurement Scale. The total score ranges from 0 to 58, with higher scores indicating better trunk control. The assessment will be administered by a physiotherapist.

  3. Posture

    Time frame: Baseline and at the end of the 8-week intervention

    Postural alignment will be assessed using the New York Posture Rating Chart. The total score ranges from 13 to 65, with higher scores indicating better postural alignment. The assessment will be performed by a physiotherapist.

  4. Handgrip Strength

    Time frame: Baseline and at the end of the 8-week intervention

    Handgrip strength will be measured in kilograms using a hand dynamometer. Three measurements will be obtained for each hand, with a 1-minute rest period between measurements. The mean value of the three measurements will be used in the analysis. Higher values indicate greater handgrip strength.

  5. Bladder and Bowel Symptoms

    Time frame: Baseline and at the end of the 8-week intervention

    Bladder and bowel symptoms will be assessed using the Bladder and Bowel Dysfunction Questionnaire. The total score ranges from 0 to 52, with higher scores indicating greater symptom severity. The questionnaire will be completed by the child with parental assistance.

  6. Familiy Quality of Life

    Time frame: Baseline and at the end of the 8-week intervention

    Family quality of life will be assessed using the Cerebral Palsy Quality of Life Questionnaire-Primary Caregiver Form (CP QOL-Child). Each domain is scored from 0 to 100, with higher scores indicating better quality of life. The questionnaire will be completed by the child's parent or primary caregiver.

Study contacts

Contact information is provided by the study sponsor or research team.

Seyda Toprak Celenay, PhD

CONTACT

[email protected]

+90 312 906 2000

Sponsors and collaborators

Lead sponsor

Fenerbahce University

Other

Registry information

Official study title

EFFECTS OF HIPPOTHERAPY ON PHYSICAL FUNCTION, BLADDER AND BOWEL SYMPTOMS, AND FAMILY QUALITY OF LIFE IN CHILDREN WITH CEREBRAL PALSY

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jul 31, 2026
Registry last updated
Jul 31, 2026

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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