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Clinical Trials/NCT06820983
NCT06820983RecruitingNot Applicable

Evaluation of the Quality of Life of Patients With DBB With the Installation of OPEP

Centre Hospitalier Universitaire, Amiens1 site in 1 country60 target enrollmentStarted: October 17, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
60
Locations
1
Primary Endpoint
Variation of patient quality of life before and after OPEP installation

Study Overview

Brief Summary

To carry out an assessment of compliance and quality of life in a population (children and adults) with DDB before and after the use of an oscillating PEP. The aim is to determine the impact of the use of oscillating PEP on the daily life of this population in particular.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
8 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Children (from 8 years of age) and adults over 18 years of age with DDB who doesn't use oscillating PEP.
  • The study population will be clinically stable and will be seen in follow-up consultations.

Exclusion Criteria

  • Children under 8 years of age.
  • Patients who use an OPEP
  • Patients in the acute exacerbation phase of their DDB
  • Patients who are not under regular consultation
  • Patients with severe, uncontrolled co-morbidities
  • Patients with cognitive or psychiatric disorders preventing proper adherence to the study protocol
  • Patients taking part simultaneously in another clinical study that could interfere with the results of the OPEP study

Outcomes

Primary Outcomes

Variation of patient quality of life before and after OPEP installation

Time Frame: 18 months

quality of life is determined by qustionnaire

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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