AzTrials
AzTrials

Cerebral Palsy (CP)DANS-SCEDNCT07500896

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

An observational study of Cerebral Palsy (CP), run by University Hospital, Toulouse at 1 site in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

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. Read more about this study

Who is it for?
Ages 6 to 17 years
Conditions the study is for
Cerebral Palsy (CP)
What is being tested?
Repeated assessments
How many people
6 participants
Where
1 siteFrance
Study dates
17 Mar 2026to 31 Dec 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 17 years
  • All sexes
  • No healthy volunteers
  • Child

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).

Who may be able to join

  • 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)

Who cannot join

  • 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)

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

France1 site, 1 recruiting
  • CHU Toulouse - Hôpital Raymonde Fournet

    Toulouse, Occitanie, 31059

    Philippe Marque, +33 5 61 77 91 08, marque.ph@chu-toulouse.fr

    Philippe MARQUE

    Recruiting

Other trials in France

About this study

Official title: 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).

Being tested
Repeated assessments
Keywords
Dance program, Cerebral palsy, Learning skills
Medical subject headings
Cerebral Palsy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Repeated assessmentsOther

    It is a multiple baseline SCED study with four successive phases (A-B-Follow UP) for each participant. Repeated assessments take place for 8 consecutive weeks, with the final assessments taking place up to one week after the end-of-year show

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Evolution of the Goal Attainment Scaling (GAS) score throughout the study

    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).

    Measured: From baseline to the final study visit (up to approximately 9 weeks)

Secondary outcomes (4)
  1. Intrinsic Motivation Inventory (IMI) scores

    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).

    Measured: From baseline to the final study visit (up to approximately 9 weeks)

  2. Physical activity levels measured by heart rate monitoring

    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).

    Measured: From baseline to the final study visit (up to approximately 9 weeks)

  3. Socio-demographic characteristics

    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.

    Measured: baseline

  4. Initial perceptions of the children

    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

    Measured: baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Mar 2026
  2. Study start17 Mar 2026
  3. Primary completion31 Dec 2026 (estimated)
  4. Study completion31 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
6 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07500896
Sponsor's protocol ID
RC31/25/0654
Acronym
DANS-SCED
Status last verified
Mar 2026
First submitted
24 Mar 2026
Last updated
30 Mar 2026
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Cerebral Palsy (CP), run by University Hospital, Toulouse at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 30 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

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)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Mar 2026.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in