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The Impact of Myofunctional Therapy on Children With Sleep Apnea and Obesity

NCT07925294, Not applicable, Not yet recruiting, Université Catholique de Louvain

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleThe Impact of Myofunctional Therapy on Children With Sleep Apnea and ObesityClinicalTrials.gov
NCT numberNCT07925294ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment62 participants, estimatedClinicalTrials.gov
Lead sponsorUniversité Catholique de LouvainClinicalTrials.gov
ConditionsObstructive Sleep Apnea (OSA) and ObesityClinicalTrials.gov
InterventionsMyofunctional therapyClinicalTrials.gov
First posted2026-11-09ClinicalTrials.gov
Last updated2026-11-09ClinicalTrials.gov

Registered outcomes 11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryApnea-hypopnea index (AHI)Throughout the entire study, during approximately 4 yearsSleep polygraphyClinicalTrials.gov
SecondaryTongue strength assessmentThroughout the entire study, during approximately 4 yearsMaximal pressure exerted by the tongue against an air-filled bulb (in kPa) in protrusion, elevation, and during swallowing.ClinicalTrials.gov
SecondaryTongue morphology assessmentThroughout the entire study, during approximately 4 yearsSubmental ultrasound in frontal and sagittal plane, to assess the thickness of tongue muscles (cm)ClinicalTrials.gov
SecondaryTongue mobility scoreThroughout the entire study, during approximately 4 yearsMotricité Bucco-Linguo-Faciale (MBLF) test, where several movements are scored between 0 and 3 regarding muscular contraction or symmetry.ClinicalTrials.gov
SecondarySleep quality questionnaireThroughout the entire study, during approximately 4 yearsThe Pediatric Sleep Questionnaire will be administered to parents. Items are answered "yes", "no", or "I don't know", and higher scores indicate more signs of obstructive sleep-disordered breathing.ClinicalTrials.gov
OtherSemi-structured interviewThroughout the entire study, during approximately 4 yearsA semi-structured interview will be conducted to collect qualitative data on sleep qualityClinicalTrials.gov
OtherTongue frenulum assessmentThroughout the entire study, during approximately 4 years
Tongue range of motion ratio, reflecting the restriction imposed by the lingual frenulum. It is computed as the maximal mouth opening with the tongue tip held at the incisive papilla (mm) divided by the maximal mouth opening (mm).
ClinicalTrials.gov
OtherBreathing pattern questionnaireThroughout the entire study, during approximately 4 yearsMouth breathing questionnaire from Abreu et al., considered positive if two major items, or one major and two minor items, are answered "yes"ClinicalTrials.gov
OtherTemporomandibular (TMD) pain screenerThroughout the entire study, during approximately 4 yearsThis questionnaire will be used to assess the presence of any temporomandibular joint disorder.ClinicalTrials.gov
Other3 questions/temporomandibular (3Q/TMD) questionnaireThroughout the entire study, during approximately 4 yearsThis questionnaire will be used to assess the presence of any temporomandibular joint disorder.ClinicalTrials.gov
OtherAdherence to rehabilitation protocolThroughout the entire study, during approximately 4 yearsAdherence will be monitored through a participation log of the rehabilitation sessions.ClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)