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Rhythm Effect on Dance Learning in Typical Development Children and Children With Motor Disorders. (DANS-APP)

T

Toulouse University Hospital

Status

Enrolling

Conditions

Cerebral Palsy (CP)

Treatments

Behavioral: With regular rhythm
Behavioral: Without regular rhythm

Study type

Interventional

Funder types

Other

Identifiers

NCT06137625
ANR-21-CE28-0031 (Other Grant/Funding Number)
RC31/22/0039

Details and patient eligibility

About

Cerebral Palsy (CP) or Developmental Coordination Disorder (DCD) leads to motor troubles impacting the everyday life, social participation and academic difficulty . According to some authors, CP and DCD pertain to a same continuum of motor disorders (MD) (Pearsall-Jones et al., 2010).Those children show an alteration in Perceptivo-Motor Procedural Learning (PMPL), corresponding to the acquisition of everyday life skill (for CP: Gagliardi et al., 2011; Gofer-Levi et al., 2013; for DCD: Gheysen et al., 2011; Blais et al., 2018). Also, recommended rehabilitation for this population are based on procedural learnings (for CP: Novak et al., 2013; for DCD: Blank et al., 2019; Inserm, 2019). It's true for dancing which present high evidence to enhance motor, cognitive, psychoaffective and social functions of this children (Cherriere, Martel, et al., 2020; Cherriere, Robert, et al., 2020). Dance is a physical activity that involve procedural learning to memorise movement sequences (choreography). Rhythm can be define as a stimuli repetition at a regular interval (Grahn & Brett, 2007; Patel, 2003). Recently studies tend to shown that rhythm is essential to enhance motor control and procedural learning (Ghai et al., 2022; Lagarrigue et al., 2021). To validate this hypothesis, the investigators will evaluate typical development children and children with CP MD learning of a dance choreography with and without rhythm.

Enrollment

68 estimated patients

Sex

All

Ages

8 to 16 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

For all the participants:

  • Aged from 8 to 16 include.
  • Free, informed, written, and signed consent of the holders of parental authority
  • Free and informed consent of the minor
  • Affiliation with or benefiting from a social security scheme.
  • Ability to understand the instructions (investigator's assessment)

For the participant with Motor disorders (MD):

  1. For children with CP:

    • CP diagnosis
    • Gross Motor Function Classification System level between I to IV.
    • Manual Ability Classification System level between I to IV.
  2. For children with DCD:

    • A diagnosis of DCD

For the participant with typical development:

  • No CP diagnosis
  • No neurological trouble nor functional disfunction including developmental coordination disorder.

Exclusion criteria

  • -Autism spectrum disorder diagnosed according to the DSM-5 (APA, 2015)
  • Hearing deficiency diagnosed according to the DSM-5 (APA, 2015) or uncorrected hearing deficiency that doesn't allows the participant to hear a music with a sound level between 45 and 70 decibels.
  • Visual deficiency diagnosed according to the DSM-5 (APA, 2015)
  • Intellectual developmental disorder diagnosed according to the DSM-5 (APA, 2015)
  • Behavioural disorders diagnosed according to the DSM-5 (APA, 2015)
  • Diagnosed epilepsia
  • Pregnancy (check in young pubescent and sexually active women) or breastfeeding.
  • Children already include in ongoing interventional study.
  • Children with both parent who benefit of legal protection (guardianship, curatorship, safeguard of justice).

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

68 participants in 2 patient groups

Motor disorders
Experimental group
Description:
Children with motor disporders
Treatment:
Behavioral: Without regular rhythm
Behavioral: With regular rhythm
Typical developing
Active Comparator group
Description:
Typical developing children
Treatment:
Behavioral: Without regular rhythm
Behavioral: With regular rhythm

Trial contacts and locations

1

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Central trial contact

David GASQ, MD; Jessica TALLET, PhD

Data sourced from clinicaltrials.gov

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