NCT05670587Completed
A Study in People With Pulmonary Fibrosis to Monitor Cough With a Wearable Device
A Multi-center, Longitudinal 12-week Pilot Study to Evaluate Cough Severity and Its Impact, Utilizing a Next Generation Cough Monitor, in Participants With Idiopathic Pulmonary Fibrosis (IPF) or Non IPF Pulmonary Fibrosis
Source: ClinicalTrials.gov · Last updated 11 Mar 2025
Brief summary (registry, in English)
This study is open to adults aged 18 years and older who have pulmonary fibrosis with or without a known cause (or other forms of pulmonary fibrosis). The purpose of this study is to better understand coughing in people with pulmonary fibrosis. To do this, a wearable cough monitor called Strados Remote Electronic Stethoscope Platform (RESP) is used. This device will measure how often and how forceful coughing is in people with pulmonary fibrosis. All participants in the study get the device. It is placed on their skin over the chest. Participants are in the study for 3 months. During this time, they visit the study site 2 to 3 times. 4 visits are done at the participant's home by video call with the site staff. During the study, the device measures coughing over 24 hours. This is done on 4 days. Participants fill in questionnaires about their coughing and doctors regularly check participant's lung function. A breathing test that measures how well the lungs are working is performed both in the office and during home visits. The doctors also regularly check participants' health and take note of any unwanted effects. This study will also record patients' experiences using the cough monitor and video assisted breathing tests at visits 3, 4, 5 and 6 at home.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 53 (actual)
- First submitted
- 15 Dec 2022
- Start date
- 16 Jan 2023
- Primary completion date
- 22 Feb 2024
- Lead sponsor
- Boehringer Ingelheim
- Diseases
- Idiopathic pulmonary fibrosis
- NCT number
- NCT05670587
What you commit to
- Study type: Interventional
- Participants enrolled: 53
- From 16 Jan 2023 to the primary completion date, 22 Feb 2024
- 13 sites in 4 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Initiation or change in dose or type of anti-tussive medication, angiotensin-converting enzyme (ACE) inhibitors, opiates, and systemic or inhaled (excluding intranasal) corticosteroids in the 4 weeks prior to study entry
- Subject with ILD exacerbation as defined by investigators within 4 weeks prior to study entry
- Subject participating in a clinical study of a systemic or inhaled drug at the time of enrollment
Other illness
- Upper Respiratory Tract Infection (URI) or Lower Respiratory Tract Infection (LRTI, including Coronavirus Disease (COVID)-19 infection) within 4 weeks of screening visit
- Airflow obstruction (Forced expiratory volume in one second (FEV1)/FVC \< 70%) at baseline or known history of significant spirometry response to bronchodilator
- Cough due to etiology other than Interstitial Lung Disease (ILD) (e.g., allergic rhinitis, Gastroesophageal Reflux Disease (GERD))
- Other respiratory disorders including, but not limited to, a current diagnosis of any obstructive disease including chronic obstructive pulmonary disease (COPD) and asthma, active tuberculosis, lung cancer in treatment or in medical history, sleep apnea, known alpha-1 antitrypsin deficiency, cor pulmonale, clinically significant pulmonary hypertension, clinically significant bronchiectasis, or other active pulmonary diseases.
Other
- Current smokers
- further exclusion criteria apply
Who the study is looking for
- Provision of signed informed consent in writing prior to study data collection
- Subject aged 18 years or over
- Subject diagnosed with Non-Idiopathic Pulmonary Fibrosis (IPF) Pulmonary Fibrosis (\>10% fibrosis on High Resolution Computed Tomography (HRCT) by principal investigator assessment) or IPF as per American Thoracic Society/European Respiratory Society/Japanese Respiratory Society/Asociación Latinoamericana de Tórax (ATS/ERS/JRS/ALAT) Guidelines within the past 12 months
- Forced Vital Capacity (FVC) \> 40% predicted at baseline visit
- Life expectancy \> 6 months (per assessment of treating physician)
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (13)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Aalst - HOSP Onze-Lieve-Vrouw Coordinator of this site? Confirm its status | Aalst | Belgium | Unknown status |
| Jessa Ziekenhuis - Campus Virga Jesse Coordinator of this site? Confirm its status | Hasselt | Belgium | Unknown status |
| Kortrijk - HOSP AZ Groeninge Kennedylaan Coordinator of this site? Confirm its status | Kortrijk | Belgium | Unknown status |
| Roeselare - HOSP AZ Delta Coordinator of this site? Confirm its status | Roeselare | Belgium | Unknown status |
| Universitätsklinikum Freiburg Coordinator of this site? Confirm its status | Freiburg im Breisgau | Germany | Unknown status |
| Universitätsklinikum Jena Coordinator of this site? Confirm its status | Jena | Germany | Unknown status |
| Rijnstate Hospital Coordinator of this site? Confirm its status | Arnhem | Netherlands | Unknown status |
| Amphia Ziekenhuis Coordinator of this site? Confirm its status | Breda | Netherlands | Unknown status |
| Erasmus Medisch Centrum Coordinator of this site? Confirm its status | Rotterdam | Netherlands | Unknown status |
| Lowcountry Lung and Critical Care Coordinator of this site? Confirm its status | Charleston | United States | Unknown status |
| Critical Care, Pulmonary and Sleep Associates Coordinator of this site? Confirm its status | Lakewood | United States | Unknown status |
| Renown Regional Medical Center Coordinator of this site? Confirm its status | Reno | United States | Unknown status |
| Southeastern Research Center Coordinator of this site? Confirm its status | Winston-Salem | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.