Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
RecruitingNot a traditional drug phaseinterventionalRules rewrite
Not a traditional drug phase: Development of a screening algorithm designed to determine a "dysmobility" profile in patients with chronic illness. for Joint Osteoarthritis
Chronic illness is a public health issue and mobility loss is frequent in this population. Among its' multiple physical and psychological consequences, increased mortality and cardiovascular morbidity seem the main concern.
This study does not use the classic phase 1–4 drug ladder. It may be a device, a behavior program, a surgery timing study, or an early feasibility test.
Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
What the registry says happens
If you join, the listed intervention(s) are Development of a screening algorithm designed to determine a "dysmobility" profile in patients with chronic illness.. The registry lists allocation as na. Chronic illness is a public health issue and mobility loss is frequent in this population.
They plan to enroll about 5,000 people at Clermont-Ferrand. Taking part typically means study visits and measurements plus check-ins.
Official title (unrewritten)
Evaluation of Impaired Mobility in Chronic Illness Constitution of a Cohort
Interventions: Development of a screening algorithm designed to determine a "dysmobility" profile in patients with chronic illness.
Primary outcome (registry wording): dismobility score calculated from the results reported in secondary outcomes
Who it is for (from inclusion criteria)
Ages 18 Years to 90 Years
Man or woman aged 18 to 90
Patients with chronic pathology contributing to impaired mobility
Volunteers who have given their written consent
Affiliated to French health care system (for France)
Who the registry excludes
Patients suffering from progressive psychiatric pathologies (active psychosis, hallucinations, etc.) or the presence of another serious unstabilized pathology (decompensated heart failure, progressive terminal cancer, etc.)
People with poorly controlled or unstable cardiovascular disease
Major osteoarticular or neurological problems completely preventing the proper performance of the various tests
Non-autonomous patient
Persons under guardianship, curatorship, deprived of liberty or safeguarding justice
Objective: This protocol is designed to allow the Surgical Neurology Branch to evaluate and treat the neurosurgical disorders of protocol participants. The participants will receive standard-of-clinical-care evaluation and treatment.
Background: \- Deep brain stimulation (DBS) is an approved surgery for certain movement disorders, like Parkinson's disease, that do not respond well to other treatments. DBS uses a battery-powered device called a neurostimulator (like a pacemaker) that is placed under the skin in the chest.
This study wants to obtain biologic materials from the blood, airways and/or urine of normal individuals and individuals with lung disease. The normal are used to establish a set of normal ranges for various parameters.
The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.
What phase is NCT04375280?
Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
Can PlainTrials tell me if I qualify for NCT04375280?
No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.