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AzTrials

BronchiectasisEQOPEPNCT06820983

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

A study testing adult questionnary for parents of children aged 8 to 13, Quality of life questionnaire for children aged 8 to 13 and Quality of life questionnaire for adolescents aged 14 to 17 in people with Bronchiectasis and Quality of Life, run by Centre Hospitalier Universitaire, Amiens at 1 site in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Ages 8 years and older
Conditions the study is for
Bronchiectasis, Quality of Life, Physiotherapy
What is being tested?
adult questionnary for parents of children aged 8 to 13, Quality of life questionnaire for children aged 8 to 13 and Quality of life questionnaire for adolescents aged 14 to 17
How many people
60 participants
Where
1 siteFrance
Study dates
17 Oct 2024to Apr 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 8 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

France1 site, 1 recruiting
  • CHU Amiens-Picardie

    Amiens, 80054

    Thomas Pinto, MD, 33+22088000, pinto.thomas@chu-amiens.fr

    Recruiting

Other trials in France

About this study

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.

Being tested
adult questionnary for parents of children aged 8 to 13, Quality of life questionnaire for children aged 8 to 13, Quality of life questionnaire for adolescents aged 14 to 17, Quality of life questionnaire for adults, A satisfaction adherence questionnaire
Keywords
quality of life, Bronchiectasis, oscillating PEP devices, physiotherapy
Medical subject headings
Bronchiectasis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • adult questionnary for parents of children aged 8 to 13Other

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

  • Quality of life questionnaire for children aged 8 to 13Other

    Quality of life questionnaire for children aged 8 to 13

  • Quality of life questionnaire for adolescents aged 14 to 17Other

    Quality of life questionnaire for adolescents aged 14 to 17

  • Quality of life questionnaire for adultsOther

    Quality of life questionnaire for adults

  • A satisfaction adherence questionnaireOther

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

What is being measured

The primary outcome is the main question the study is designed to answer.

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

    quality of life is determined by qustionnaire

    Measured: 18 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Feb 2025
  2. Study start17 Oct 2024
  3. Primary completionApr 2026 (estimated)
  4. Study completionApr 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Not applicable
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06820983
Sponsor's protocol ID
PI2024_843_0118
Acronym
EQOPEP
Status last verified
Jan 2026
First submitted
6 Feb 2025
Last updated
23 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing adult questionnary for parents of children aged 8 to 13, Quality of life questionnaire for children aged 8 to 13 and Quality of life questionnaire for adolescents aged 14 to 17 in people with Bronchiectasis and Quality of Life, run by Centre Hospitalier Universitaire, Amiens at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 23 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Thomas PINTO, MD (33+3 22 08 80 00, pinto.thomas@chu-amiens.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Variation of patient quality of life before and after OPEP installation (time frame: 18 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jan 2026.

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