Thinking and balancing: new study reveals hidden fall risk for COPD patients
NCT ID NCT06863246
First seen Jun 27, 2026 · Last updated Jul 08, 2026 · Updated 2 times
Summary
This study looked at how doing a mental task while standing affects balance in people with chronic lung disease (COPD). Researchers compared 36 adults with COPD to healthy volunteers to see if their balance got worse when they had to think at the same time. The goal was to better understand fall risks and help design safer daily activities.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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36 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Mar 2025
- 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.
Who is studied
Participants enrolled in NEUROTIGUE study (NCT04028973)
- Ages
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40 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: COPD patients : * GOLD II - III or IV * FEV1 \<80% of predicted values * Men and women aged 40 years and over * French-speaking participant * BMI \<30 kg / m² * Stable condition (i.e. without exacerbation) for more than 15 days * Able to express their consent in writing prior to any participation in the study * Affiliates or beneficiaries of a social security * Minimum score of 26 on the MMSE questionnaire of 3 months or less Healthy volunteers : * Men and women aged 40 years and over * French-speaking participant * BMI \<30 kg / m² * No known chronic respiratory, cardiovascular, metabolic, renal or neuromuscular pathologies * Able to express their consent in writing prior to any participation in the study * Affiliates or beneficiaries of a social security * Minimum score of 26 on the MMSE questionnaire of 3 months or less For all participants : -Subject who has not objected to the reuse of data collected Exclusion Criteria: * COPD patients : * Alcoholism, i.e. \> 21 glasses a week for men and \>14 glasses a week for women * Psychiatric pathologies or antecedent of behavioral disorders * Patients treated with oral or systemic corticosteroids (\> 0.5 mg / kg / day for \> 7 days) * Contraindication to the application of a magnetic field (i.e. right hip arthroplasty, pelvic / abdominal surgeries) * Severe vision or hearing problems not corrected * Patient oxygen dependent * Patients in exclusion period from another research protocol * Pregnant women (known pregnancy) or lactating women * Patient deprived of liberty by a judicial or administrative decision * Patient subject to a legal protection measure or unable to express their consent * Patient who is not sufficiently fluent in reading and understanding the French language to be able to consent to participate in the study * Patient unable to follow study procedures and to respect visits throughout the study period * Person with a medical history that, in the opinion of the investigator, could interfere with the results of the study * Any condition that, in the opinion of the investigator, could increase and compromise the safety of the person in the event that he / she participates in the study * Any other reason that, in the opinion of the investigator, could interfere with the evaluation of the aims of the study Healthy volunteers: * Alcoholism, i.e. \> 21 glasses a week for men and \>14 glasses a week for women * Psychiatric pathologies or antecedent of behavioral disorders * Patients treated with oral or systemic corticosteroids (\> 0.5 mg / kg / day for \> 7 days) * Contraindication to the application of a magnetic field (i.e. right hip arthroplasty, pelvic / abdominal surgeries) * Severe vision or hearing problems not corrected * Subjects in exclusion period from another research protocol * Pregnant women (known pregnancy) or lactating women * Regular physical activity with a frequency greater than 3 sessions per week * Participant deprived of liberty by a judicial or administrative decision * Participant subject to a legal protection measure or unable to express their consent * Participant who is not sufficiently fluent in reading and understanding the French language to be able to consent to participate in the study * Participant unable to follow study procedures and to respect visits throughout the study period * Person with a medical history that, in the opinion of the investigator, could interfere with the results of the study * Any condition that, in the opinion of the investigator, could increase and compromise the safety of the person in the event that he / she participates in the study * Any other reason that, in the opinion of the investigator, could interfere with the evaluation of the aims of the 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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Université de Toulon - Laboratoire J-AP2S
Toulon, VAR, 83100, France
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Other studies related to the condition(s) this trial covers.
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