Evaluating patient experiences and outcomes for bronchoscopic procedures
Patient Reported Outcome and Experience Measures for Bronchoscopic Procedures
Vitaz · NCT06307379
This study is trying to understand how patients feel and what their experiences are like during bronchoscopic procedures to help improve care for future patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 300 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Vitaz (other) |
| Locations | 1 site (Sint-Niklaas) |
| Trial ID | NCT06307379 on ClinicalTrials.gov |
What this trial studies
This observational study focuses on gathering patient-reported outcome measures (PROMs) and patient-reported experience measures (PREMs) specifically for bronchoscopic procedures. By collecting and analyzing these reports, the study aims to improve the quality of care, monitor health status, and enhance decision-making in healthcare financing. The study will involve patients over 18 years old who are referred for outpatient diagnostic flexible bronchoscopy, ensuring that their experiences and outcomes are documented and integrated into clinical practices. No interventions will be applied, as the emphasis is on observational data collection.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old who are referred for outpatient diagnostic flexible bronchoscopy.
Not a fit: Patients who are unable to respond to the questionnaire or those undergoing the procedure in a hospitalized setting may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved patient care and satisfaction in bronchoscopic procedures.
How similar studies have performed: While there is limited literature on PROMs and PREMs specific to bronchoscopic procedures, the approach of utilizing patient-reported measures has shown success in other medical fields.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age above 18 years * Patient referred for diagnostic flexible bronchoscopy * Procedure performed in outpatient setting Exclusion Criteria: * Patient unable to adequately respond to the contents of the patient questionnaire. * Procedure performed in hospitalised setting * Patient with active pregnancy
Where this trial is running
Sint-Niklaas
- VITAZ — Sint-Niklaas, Belgium (RECRUITING)
Study contacts
- Principal investigator: Jonas Yserbyt, MD, PhD — MD
- Study coordinator: Jonas Yserbyt, MD,PhD
- Email: jonas.yserbyt@vitaz.be
- Phone: +3237602327
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: Bronchial Diseases, bronchoscopy, endoscopy, patient reported outcome measures