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NCT Number: NCT06820983

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

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.

Recruiting

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Key information

Age range

8 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU Amiens-Picardie

Amiens, 80054, France

Location status: Recruiting

Location contact

Thomas Pinto, MD

CONTACT

[email protected]

33+22088000

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

adult questionnary for parents of children aged 8 to 13

Other

Quality of life questionnaire for parents of children aged 8 to 13

Quality of life questionnaire for children aged 8 to 13

Other

Quality of life questionnaire for children aged 8 to 13

Quality of life questionnaire for adolescents aged 14 to 17

Other

Quality of life questionnaire for adolescents aged 14 to 17

Quality of life questionnaire for adults

Other

Quality of life questionnaire for adults

A satisfaction adherence questionnaire

Other

A satisfaction adherence questionnaire will also be distributed to patients after several months' use of oscillating PEP

Primary outcomes

  1. Variation of patient quality of life before and after OPEP installation

    Time frame: 18 months

    quality of life is determined by qustionnaire

Study contacts

Contact information is provided by the study sponsor or research team.

Thomas PINTO, MD

CONTACT

[email protected]

33+3 22 08 80 00

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire, Amiens

Other

Collaborators

  • Hôpital Armand Trousseau

Registry information

Acronym: EQOPEP

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Feb 11, 2025
Registry last updated
Jan 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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