Comparing two methods of cheek support during lung function testing
Comparative Evaluation of the Use of a Mouthpiece With Integrated Cheek Support vs. Manual Cheek Support During Respiratory Oscillometry Measurements
NA · Politecnico di Milano · NCT06537362
This study tests which cheek support method during lung function tests—manual support by an expert or a built-in mouthpiece—helps people feel more comfortable and gives more accurate results.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 55 (estimated) |
| Ages | 5 Years to 75 Years |
| Sex | All |
| Sponsor | Politecnico di Milano (other) |
| Locations | 1 site (Bergamo) |
| Trial ID | NCT06537362 on ClinicalTrials.gov |
What this trial studies
This study evaluates the accuracy of respiratory impedance measurements during oscillometry using two different cheek support methods: manual support by an expert and an integrated cheek support in a mouthpiece. It is a prospective, randomized, cross-over study involving participants aged 5 to 75 years who will undergo measurements of facial morphology and respiratory impedance. The study aims to assess not only the measurement accuracy but also the comfort level of patients during the procedure. Participants will complete a questionnaire regarding their comfort after the measurements.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged between 5 and 75 years who can follow study procedures.
Not a fit: Patients with physical or mental conditions that prevent them from participating in the study may not benefit.
Why it matters
Potential benefit: If successful, this study could improve the accuracy and comfort of lung function testing for patients.
How similar studies have performed: While similar approaches have been explored, this specific comparison of cheek support methods in respiratory oscillometry is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * subjects aged between 5 and 75 years Exclusion Criteria: * Subjects unable to follow the study procedures or with any physical or mental condition deemed unsuitable by the doctor will be excluded from the study
Where this trial is running
Bergamo
- Allergy and Pneumology Outpatient Clinic — Bergamo, Italy (RECRUITING)
Study contacts
- Study coordinator: Raffale Dellaca, PhD
- Email: raffaele.dellaca@polimi.it
- Phone: 0223999005
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Respiratory Morbidity, Lung Function Decreased, Oscillometry