Patient Reported Outcome and Experience Measures for Bronchoscopic Procedures

Last updated: March 11, 2024
Sponsor: Vitaz
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

no intervention

Clinical Study ID

NCT06307379
EC 23022
  • Ages > 18
  • All Genders

Study Summary

'Patient-reported outcomes' (PROMS) and 'patient-reported experiences' (PREMS) are increasingly important parameters in evaluating and adjusting clinical procedures and strategies in healthcare.

Validated disease-specific PROMS related to bronchoscopic procedures are not available and examples in the medical literature are very scarce.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age above 18 years
  • Patient referred for diagnostic flexible bronchoscopy
  • Procedure performed in outpatient setting

Exclusion

Exclusion Criteria:

  • Patient unable to adequately respond to the contents of the patient questionnaire.
  • Procedure performed in hospitalised setting
  • Patient with active pregnancy

Study Design

Total Participants: 300
Treatment Group(s): 1
Primary Treatment: no intervention
Phase:
Study Start date:
February 13, 2024
Estimated Completion Date:
December 30, 2025

Study Description

The potential usefulness of PROM/PREMS is multiple:

  1. Quality improvement within the current clinical care structure

  2. Monitoring the health status of the population

  3. Contribution to decision-making regarding financing of care

  4. Increase employee and patient involvement in clinical care pathways

  5. Rationalize the deployment of medical personnel and resources

  6. Integration of data in electronic patient files and registers

Connect with a study center

  • VITAZ

    Sint-Niklaas,
    Belgium

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.