Premalocom1: Early Intervention Based on Neonatal Crawling in Very Premature Infants Without Major Brain Damage

Sponsor
Marianne Barbu-Roth (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05278286
Collaborator
Ecole Pratique des Hautes Etudes (Other)
48
2
3
91.2
24
0.3

Study Details

Study Description

Brief Summary

Extreme prematurity is constantly increasing according to the World Health Organization. However, methods to train premature infants at risk of disability is sorely lacking. The goal of this project is to overcome this problem. In our previous studies, we discovered that promoting the crawling of typical newborns on a mini skateboard, the Crawliskate (a new tool that we designed and patented EP2974624A1), is an excellent way to stimulate infants' motor and locomotor development. This method is a promising way to provide early interventions in infants at heightened risk for developmental delay, such as premature infants.

The specific objective of this study is to determine if early training in crawling on this mini skateboard will accelerate motor (particularly locomotor) and/or neuropsychological development in very premature infants identified as median risk for developmental delay.

Methodology: We will study and follow three groups of very premature infants born between 24 and 32 weeks of gestational age without major brain lesions. These infants will be recruited before their hospital discharge at the NICU. After their discharge from the hospital, one group of infants will be trained at home by physiotherapists to crawl on the Crawliskate every day for 2 months (Crawli group), one group of infants will be trained at home by physiotherapists positioned prone on a mattress (Mattress group) and one group of infants will receive regular medical care (Control group). All infants will be tested for: 1) their crawling proficiency on the Crawliskate at term-equivalent age (just before training for the trained groups) and at 2 months corrected age (CA, i.e., age determined from the date on which they should have been born), 2) their motor proficiency between 2 and 24 months CA (2D and 3D recording of head control, sitting, crawling, stepping, walking) and 3) their neurodevelopmental, motor and neuropsychological development between 0 and 24 months CA : BSID III edition, ASQ-3, Amiel-Tison's Neurological Assessment, Prechtl Assessment of general movements. One more ASQ-3 questionnaire will be provided at five years.

Expected results: Our first research hypothesis is that premature infants trained daily to crawl (for two months after discharge from the NICU) will acquire proficient crawling patterns and develop earlier and more effective motor and neuropsychological development than premature infants who receive mattress training or no training.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Crawling stimulation with the crawliskate
  • Behavioral: Tummy time without the crawliskate
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
48 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effects of Early Crawling Training on the Motor Development of Very Premature Infants Without Major Brain Damage
Actual Study Start Date :
Mar 27, 2017
Actual Primary Completion Date :
Nov 15, 2021
Anticipated Study Completion Date :
Nov 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Crawli Group

Participants from the Crawli Group will benefit from the crawling stimulation intervention with the crawliskate

Behavioral: Crawling stimulation with the crawliskate
Consists of 2 months of daily training. Infants benefit from a 5 minutes session everyday at home with a trained therapist. During each session the infant is prone wrapped on the crawliskate and has to produce flexion and extension movements with his four limbs in order to move forward with the assistance of the therapist.

Active Comparator: Mattress Group

Participants from the Mattress Group will benefit from the tummy time intervention

Behavioral: Tummy time without the crawliskate
Consists of 2 months of daily training. Infants benefit from a 5-minutes session everyday at home with a trained therapist. During each session the infant is prone directly ona mattress and cannot benefit from any assistance from the therapist to move forward.

No Intervention: Control Group

Control group infants benefit from usual care.

Outcome Measures

Primary Outcome Measures

  1. Gross motor score from the Bayley Scale of Infant and toddlers Development III ed. [12 months corrected age]

    The Bayley Scale of Infant and toddlers Development III ed. (BSID III) assesses several aspect of development: motor, fine motor, communication, personal social, language and problem solving domain. A score can be obtained for each aspect. At 12 months corrected age we only evaluate gross and fine motor scores, and we consider the gross motor score obtained at 12 months corrected age as the primary outcome of our study. The minimal score is 0 and there is no maximal score (the child is asked to complete several tasks, and the test can continues with questions from an upper age and only stops when a child no longer succeed with the tasks to complete). A higher score means more advanced skills.

Secondary Outcome Measures

  1. Amiel-Tison Neurological Assessment [at 37-41 gestational age, 2, 6, 9, 12, 24 months corrected age]

    Infant neurological examination at study entry and after the training

  2. Prechtl assessment [at 37-41 gestational age and 2 months corrected age]

    General movements assessment by video recording: measures the fluency and variability of spontaneous movement while the infant is lying supine on a mattress

  3. Age and Stage questionnaire (ASQ) 3 [2, 6, 9, 12, 18, 24 corrected age and 5 years]

    Parental appreciation of their infant development in personal-social, communication, gross motor, fine motor and problem solving domain The minimal score is 0 and the maximal score is 60. A higher score means more advanced skills.

  4. 2D & 3D analysis of movement [at 37-41 gestational age, 2, 6, 9, 12, 24 months corrected age]

    2D & 3D analysis of movement (head control, sitting, crawling, stepping, walking) using qualysis and gaitrite system

  5. All scores from the Bayley Scale of Infant and toddlers Development III ed. [24 months corrected age]

    The Bayley Scale of Infant and toddlers Development III ed. (BSID III) assesses several aspect of development: motor, fine motor, communication, personal social, language and problem solving domain. A score can be obtained for each aspect. At 24 months corrected age we evaluate the score from each aspect. The minimal score is 0 and there is no maximal score (the child is asked to complete several tasks, and the test can continues with questions from an upper age and only stops when a child no longer succeed with the tasks to complete). A higher score means more advanced skills.

  6. Fine and gross motor scores from the Bayley Scale of Infant and toddlers Development III ed. [2, 6, 9, 12, 18 months corrected age]

    The Bayley Scale of Infant and toddlers Development III ed. (BSID III) assesses several aspect of development: motor, fine motor, communication, personal social, language and problem solving domain. A score can be obtained for each aspect. At 2, 6, 9, 12 and 18 months corrected age we only evaluate fine and gross motor scores. Note that the gross motor score obtained at 12 months corrected age is the primary outcome of our study but the fine motor score obtained at 12 months corrected age is also a secondary outcome. The minimal score is 0 and there is no maximal score (the child is asked to complete several tasks, and the test can continues with questions from an upper age and only stops when a child no longer succeed with the tasks to complete). A higher score means more advanced skills.

Eligibility Criteria

Criteria

Ages Eligible for Study:
37 Weeks to 42 Weeks
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Term between 24-32 GA

  • parental consent

  • family living in intervention area

  • good tolerance on the first crawliskate trial

Exclusion Criteria:
  • no bronchodysplasia define by oxygen dependency after 36 GA

  • no medical disease

  • no limb deformity

  • no karyotype anomaly

  • no visual or auditory inpairment

Contacts and Locations

Locations

Site City State Country Postal Code
1 APHP Paris Ile De France France 75019
2 Cnrs Umr 8002 Paris Ile-de-France France 75006

Sponsors and Collaborators

  • Marianne Barbu-Roth
  • Ecole Pratique des Hautes Etudes

Investigators

  • Study Chair: Marianne Barbu-Roth, PhD, Centre National de la Recherche Scientifique, France
  • Principal Investigator: ValĂ©rie Biran, MD, PhD, APHP

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Marianne Barbu-Roth, Principal Investigator, Centre National de la Recherche Scientifique, France
ClinicalTrials.gov Identifier:
NCT05278286
Other Study ID Numbers:
  • Premalocom1
  • ANR-20-CE17-0014
First Posted:
Mar 14, 2022
Last Update Posted:
Jul 19, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 19, 2022