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
Study Sites (1)
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