Menu
Recruiting NCT07273019

Tongue Muscular Assessment in Children With Sleep Disordered Breathing

No phase Interventional Obstructive Sleep Apnea

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Tongue Strength Assessment, Polysomnography, Subjective Assessment of Sleep-Disordered Breathing, Subjective Assessment of Daytime Functioning.
Who it may be relevant to
Registry conditions: Obstructive Sleep Apnea. Basic parameters: 4 years — 17 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Tongue Muscular Assessment in Children Referred for Polysomnography in a Context of Suspected Obstructive Sleep Apnea

Overview

Obstructive sleep apnea (OSA) is part of the sleep-disordered breathing spectrum. Its prevalence in children is 1-5%, and it can have negative consequences at the cardiovascular, cognitive as well as behavioral levels. In children, the first-line treatment is adenotonsillectomy. However, residual obstructive events can persist as the success rate of surgery reaches only 49% in non-obese children. Residual OSA may be explained by multiple sites of obstruction, found in 20-85% children concerned by persistent OSA. Indeed, the tongue appears among one possible primary sites of obstruction. Given the tongue's crucial role in upper-airway patency during sleep, its assessment can inform us about the myofunctional deficits involved in sleep-disordered breathing. The primary objective of the present study is to assess tongue motor functions in children with sleep-disordered breathing and to compare them to those of healthy children (data collected in a current study (TMAC) conducted at UCLouvain, Belgium; NCT06166680), in order to document possible myofunctional deficits in children with OSA. The hypothesis is that tongue motor functions will be lower in children with sleep-disordered breathing.

Interventions

  • Other Tongue Strength Assessment
    The following items will be assessed: 1. Tongue peak pressure during 3 seconds of tongue protrusion 2. Tongue peak pressure (i.e., the maximal pressure - Pmax - exerted against the IOPI bulb) during 3 seconds of tongue elevation 3. Tongue pressure (in kPa) exerted against the IOPI (Iowa Oral Performance Instrument) bulb while swallowing
  • Diagnostic test Polysomnography
    Patients will undergo full-night polysomnography (including the JAWAC system to record mandibular movements) in the sleep unit of Hôpital Femme-Mère-Enfant (Bron, France) to explore OSA.
  • Other Subjective Assessment of Sleep-Disordered Breathing
    The following questionnaires will be filled out: * OSA-18 * Pediatric Sleep Questionnaire (PSQ) * Spruyt \& Gozal * Sleep Disturbance Scale for Children * Abreu et al.'s questionnaire
  • Other Subjective Assessment of Daytime Functioning
    The following questionnaires will be filled out: * Epworth Sleepiness Scale * Conners
  • Other Anthropometry
    The following measures will be collected via the Quick Tongue-Tie Assessment tool: 1. Maximal mouth opening 2. Maximal mouth opening with tongue to palate
  • Other Clinical Examination
    The following variables will be collected during a clinical examination: 1. Age 2. Sex 3. Weight 4. Height 5. BMI 6. Friedman score 7. Mallampati score 8. Medical history
  • Other Orofacial Praxis Assessment
    Bucco-Linguo-Facial Motor Skills will be assessed through the test "Motricité Bucco-Linguo-Faciale" (MBLF).

Primary outcome measures

  • Tongue peak pressure during protrusion [Time frame: Day 1]
Secondary outcome measures (12)
  • Tongue peak pressure during elevation and swallowing [Time frame: Day 1]
  • Tongue mobility restriction [Time frame: Day 1]
  • Orofacial praxis [Time frame: Day 1]
  • Obstructive apnea-hypopnea index (OAHI) [Time frame: Day 1]
  • Central apnea-hypopnea index [Time frame: Day 1]
  • Mixed apnea-hypopnea index [Time frame: Day 1]
  • Respiratory effort index [Time frame: Day 1]
  • Respiratory effort-related arousal index (RERA) [Time frame: Day 1]
  • Mean CO2 [Time frame: Day 1]
  • Max CO2 [Time frame: Day 1]
  • Time spent with CO2 > 50mmHg [Time frame: Day 1]
  • Mean SpO2 [Time frame: Day 1]

Eligibility criteria

Inclusion criteria

  • With suspected sleep-disordered breathing
  • Referred for polysomnography
  • Affiliated to a social security scheme
  • With informed consent from both legal representatives

Exclusion criteria

  • Insufficient comprehension of French language
  • Regarding patients with suspected OSA type I or II:
  • Neurological, cardiac, or unstable respiratory conditions other than sleep disorders and their repercussions
  • Any deficit possibly impacting measurements according to the investigator (e.g., psychiatric condition)
  • Malformation of the skull, the upper airway or the oral cavity
  • Regarding patients with suspected OSA type III:
  • Any deficit possibly impacting measurements according to the investigator (e.g., psychiatric condition)
  • Intellectual deficit impeding the understanding of instructions

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Basic science

Study locations

France · 1 center
  • Hôpital Femme-Mère-Enfant : Service d'épileptologie clinique, des troubles du sommeil et d — Bron

Identifiers

NCT: NCT07273019 · 69HCL25_0288 · 2025-A01527-42

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗