Effects of an Intensive Rhythmic Dance Program on Learning Skills in Children With Cerebral Palsy (DANS-SCED)

March 24, 2026 updated by: University Hospital, Toulouse

Effects of an Intensive Rhythmic Dance Program on Learning Ability in Children With Cerebral Palsy

Cerebral palsy is a neurological disorder that affects 1 in 1,000 children and causes motor disability , with sometimes sensorymotor disability which have consequences on daily life. The aim of rehabilitation for people with cerebral palsy is to improve patients' independence and quality of life. A major stake for these people is therefore to learn new behaviors by fostering motor, cognitive, and psychosocial development. Dance is a relevant activity, as it is a physical and enjoyable learning activity and a multisensory environment. Moreover, scientific literature suggests motor and psycho-affective benefits associated with dance practice in children with cerebral palsy, especially when it involves rhythmic stimulation. The aim of this project is therefore to assess the effect of a rhythm-based dance program on motor learning ability, as rhythmic auditory stimulation can improve motor control in patients with other neurological disorders (e.g., Thaut, 2015). We suppose that being able to synchronize through the practice of rhythmic dance could facilitate the learning of cognitive and psychosocial motor skills.

To reach this goal, we will conduct a Single Case Experimental Study (SCED). Using this individual analysis method, we will repeatedly evaluate a target behavior to determine whether a dance program facilitates motor, cognitive, and psychosocial learning for each participant.

The dance program will take place over two weeks. Three instructors will lead dance classes (two 2-hour sessions per day with breaks) during the first week, and three one-hour dance classes during the second week. Assessments will be conducted before (baseline, phase A), during (intervention, phase B), after the dance workshop (follow-up phase, FU), and far from it (final study visit).

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

6

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Occitanie
      • Toulouse, Occitanie, France, 31059
        • Recruiting
        • CHU Toulouse - Hôpital Raymonde Fournet
        • Contact:
        • Principal Investigator:
          • Philippe MARQUE

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Participants with cerebral palsy will be recruited from ASEI ((Agir, Soigner, Eduquer, Insérer), a public utility organization governed by the French law of July 1, 1901).

Description

Inclusion Criteria:

  • Age between 6 and 17 years old
  • Diagnosis of cerebral palsy
  • Level I to IV on the Gross Motor Function Classification System (GMFCS, Palisano et al., 2008) : with or without an armchair
  • Level I to IV on the Manual Ability Classification System (MACS, Eliasson et al., 2006)
  • Affiliation with or beneficiary of a Social Security scheme
  • Ability to understand instructions (investigator's assessment)

Exclusion Criteria:

  • Autism spectrum disorder diagnosed according to DSM-5 criteria (APA, 2013)
  • Hearing impairment diagnosed according to DSM-5 criteria (APA, 2013) or uncorrected hearing impairment that prevents the individual from hearing music at a volume between 45 and 70 decibels
  • Visual impairment diagnosed according to DSM-5 criteria (APA, 2013) and uncorrected
  • Intellectual Developmental Disorder diagnosed according to DSM-5 criteria (APA, 2013)
  • Behavioral/conduct disorders diagnosed according to DSM-5 criteria (APA, 2013)
  • Child enrolled in a dance program specifically focused on rhythm
  • Child whose parents are both subject to legal protection measures (guardianship, curatorship, judicial protection)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evolution of the Goal Attainment Scaling (GAS) score throughout the study
Time Frame: From baseline to the final study visit (up to approximately 9 weeks)
The main criterion is the evolution of the Goal Attainment Scaling (GAS) score throughout the study. The GAS corresponds to the individual goals set with each child at the beginning of the study. Three individualized and specific goals will be defined for each child, covering motor, cognitive, and psychosocial domains. These measurements will be assessed repeatedly during the dance program: reference phase (baseline, phase A), during the dance program (intervention, phase B), and after the dance program (follow-up phase, FU), with a final assessment at a distance from the intervention phase (final study visit).
From baseline to the final study visit (up to approximately 9 weeks)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Intrinsic Motivation Inventory (IMI) scores
Time Frame: From baseline to the final study visit (up to approximately 9 weeks)
Children's perceptions will be assessed using the Intrinsic Motivation Inventory adapted for children with cerebral palsy ). This questionnaire evaluates interest and enjoyment in performing an activity, skills involved perception, perceived value and activity usefulness, the feeling of freedom and choice, and perceived pressures and tensions. These measurements will be assessed repeatedly during the dance program: reference phase (baseline, phase A), during the dance program (intervention, phase B), and after the dance program (follow-up phase, FU), with a final assessment at a distance from the intervention phase (final study visit).
From baseline to the final study visit (up to approximately 9 weeks)
Physical activity levels measured by heart rate monitoring
Time Frame: From baseline to the final study visit (up to approximately 9 weeks)
Physical activity levels will be measured using a heart rate monitor. These measurements will be assessed repeatedly during phase A, during the dance program (phase B), and after the dance program (follow-up phase, FU). A final assessment will be conducted remotely after the intervention phase (final study visit).
From baseline to the final study visit (up to approximately 9 weeks)
Socio-demographic characteristics
Time Frame: baseline
Socio-demographic characteristics is a composite measure derived age, sex, practice habits (Physical Activity (PA), dance, PA related to rhythm) will be collected via an interview grid at the beginning of the study.
baseline
Initial perceptions of the children
Time Frame: baseline
The initial perceptions of the children and their parents regarding their self-image in relation to dance (perceived ability and expected progress) and the effects of the dance program will be collected at the beginning of the study using a semi-structured interview, and the evolution of these perceptions will be analyzed qualitatively
baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 17, 2026

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

March 24, 2026

First Submitted That Met QC Criteria

March 24, 2026

First Posted (Actual)

March 30, 2026

Study Record Updates

Last Update Posted (Actual)

March 30, 2026

Last Update Submitted That Met QC Criteria

March 24, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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