Smart wristband aims to catch COPD attacks early
NCT ID NCT05759247
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a remote monitoring wristband (Bora Care) to see if it can detect early signs of worsening COPD. 64 people with COPD who have had recent flare-ups are being followed. The goal is to see if the device can alert patients and doctors before a serious attack happens.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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64 people
The number who actually took part.
- Started
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Jun 2023
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient with COPD defined according to the SPLF recommendations, whose level of lung function in a stable state is known (measurement less than 12 months old) * Patient with at least one of the following criteria : * Hospitalized for a COPD exacerbation at the time of enrolment in the study, and having had at least one other exacerbation in the last 12 months * Followed-up and part of the active file of the site, having had at least 2 exacerbations during the last 12 months, including one with hospitalization * COPD patient with at least 2 exacerbations in the last 12 months, including one with hospitalization * Patient having given written informed consent to participate in the study * Patient affiliated to the French social security system Exclusion Criteria * Vulnerable patient (minor, protected adult, prisoner) * Patient unable to use the BoraBand tool and without access to a caregiver * Presence of a comorbidity considered unstable or very severe by the investigator * Patient already participating in another interventional research study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Pneumology Department - Hôpital Cochin
Paris, 75014, France
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