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NCT07370350Recruiting

Ultrasound Assessment of Tongue Characteristics in Children and Adolescents With Obesity

Standardized Tongue Ultrasound Protocol for Tongue Characteristics in Children and Adolescents With Obesity After a 30-week Inpatient Weight Loss Program

Source: ClinicalTrials.gov · Last updated 27 Jan 2026

Brief summary (registry, in English)

This longitudinal observational study aims to validate ultrasound-based tongue markers related to tongue characteristics, including fat accumulation, morphologic and mechanical properties of the tongue in children and adolescents with obesity. Participants are assessed at baseline and after completion of a standardized 30-week inpatient weight-loss rehabilitation program at the Zeepreventorium (De Haan, Belgium). Tongue ultrasound parameters are examined in relation to anthropometric characteristics and obstructive sleep apnea condition.

Status (registry)
Recruiting
Study type
Observational
Enrollment
100 (estimated)
First submitted
3 Jan 2026
Start date
1 Apr 2025
Primary completion date
1 Jul 2026
Lead sponsor
Haute Ecole Bruxelles-Brabant
Diseases
Obesity
NCT number
NCT07370350

What you commit to

  • Study type: Observational
  • Planned participants: 100
  • From 1 Apr 2025 to the primary completion date, 1 Jul 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Known orthopedic, traumatic, or rheumatologic conditions affecting the cervicocephalic region

Other

  • Contraindication to ultrasound examination
  • Inability to comply with study procedures
  • Inability to understand the procedures

Who the study is looking for

  • Children and adolescents aged 6 to 18 years
  • Diagnosis of obesity
  • Already enrolled in the inpatient weight-loss rehabilitation program at the Zeepreventorium
  • Written informed consent from legal guardian and assent from the participant, following the legal requirements

Age in the registry: 6 years to 18 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
ISEK-HE2B, av. Schalle 91
Coordinator of this site? Confirm its status
BrusselsBelgiumRecruiting
Zeepreventorium Koninklijke Baan 5
Coordinator of this site? Confirm its status
De HaanBelgiumNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.