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Therapeutic Dance Intervention for Children With Cerebral Palsy

A Pilot Study of a Therapeutic Dance Intervention for Children With Cerebral Palsy

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03681171
Enrollment
9
Registered
2018-09-21
Start date
2016-10-06
Completion date
2017-06-15
Last updated
2026-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Palsy

Brief summary

Children with cerebral palsy (CP) have motor impairments that may limit participation in standard physical activity (PA) programs. Adapted PA interventions may help address this gap. Dance-based interventions may support coordination, posture, muscle strength, motor learning, and executive function. This pilot study evaluates the feasibility and preliminary effects of a therapeutic ballet intervention designed for children with CP on physiological and executive function outcomes.

Detailed description

Eight children with cerebral palsy (CP), ages 9 to 14 years, participated in a six-week therapeutic ballet intervention. Participants underwent pre- and post-intervention assessments of body composition by dual-energy X-ray absorptiometry (DXA), muscle strength by hand-grip dynamometry, habitual physical activity, gait, selective motor control, and executive function. Follow-up assessments of habitual physical activity, gait, and executive function were completed 4 to 5 weeks after the intervention.

Interventions

Participants attended therapeutic ballet sessions three times per week for six weeks.

Sponsors

Shlomit Aizik
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
9 Years to 15 Years
Healthy volunteers
No

Inclusion criteria

* Cerebral palsy spastic diplegia and/or hemiplegia * Absence of health problems that would preclude participation in exercise * Male or female age 9 - 15 years inclusive at the time of consent * Minimum level of intellectual functioning (e.g., as determined by an IQ score of 80 or above or other education placement and testing indicating sufficient understanding) * Ability to complete study measures at the assessment * Ability to participate in dance classes conducted in English * Interest in learning ballet * Intact vision * Intact hearing * Able to ambulate independently in the community with or without a device * Intact proprioception in lower extremities * Able to complete assessment measures and consents in English * Referral from the child's pediatrician or other physician indicating that the child is physically able to participate in an exercise intervention

Exclusion criteria

* Children with a current diagnosis of severe Major Depressive Disorder * Generalized Anxiety Disorder * Epilepsy * Autism * Other major medical conditions that prohibit full participation and children with severe developmental disorders (e.g., mental retardation, severe autism) or with physical impairments that prohibit full participation were excluded from the study.

Design outcomes

Primary

MeasureTime frameDescription
Congruent Trial (Hearts) Accuracy12 weeksInhibitory control, working memory, and cognitive flexibility (hearts and flowers computer task) The scale title is Accuracy (%) and the measurement is percent correct, where the higher scores mean better results and more accuracy. Accuracy ranges from about 20%-100%
Congruent Trial (Hearts) Response Time12 weeksInhibitory control, working memory, and cognitive flexibility (hearts and flowers computer task) The scale title is Response Time in milliseconds (ms), the lower the number the better the score. The range is about 550ms-1100ms.
Incongruent Trial (Flowers) Accuracy12 weeksInhibitory control, working memory, and cognitive flexibility (hearts and flowers computer task) The scale title is Accuracy (%) and the measurement is percent correct, where the higher scores mean better results and more accuracy. Accuracy ranges from about 20%-100%
Incongruent Trial (Flowers) Response Time12 weeksInhibitory control, working memory, and cognitive flexibility (hearts and flowers computer task) The scale title is Response Time in milliseconds (ms), the lower the number the better the score. The range is about 550ms-1100ms.
Mixed Trial (Hearts and Flowers) Accuracy8 weeksInhibitory control, working memory, and cognitive flexibility (hearts and flowers computer task) The scale title is Accuracy (%) and the measurement is percent correct, where the higher scores mean better results and more accuracy. Accuracy ranges from about 20%-100%
Mixed Trial (Hearts and Flowers) Response Time8 weeksInhibitory control, working memory, and cognitive flexibility (hearts and flowers computer task) The scale title is Response Time in milliseconds (ms), the lower the number the better the score. The range is about 550ms-1100ms.

Contacts

STUDY_DIRECTORShlomit Aizik, PhD

University of California, Irvine

Participant flow

Pre-assignment details

Each group contained the same participants

Baseline characteristics

Characteristic
Age, Categorical
<=18 years
8 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
0 Participants
Sex: Female, Male
Female
6 Participants
Sex: Female, Male
Male
2 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 9
other
Total, other adverse events
0 / 9
serious
Total, serious adverse events
0 / 9

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026