App and wearable track daily struggles of arthritis patients
NCT ID NCT07167784
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a smartphone app and a wearable activity tracker are practical and acceptable for people with inflammatory rheumatic diseases like rheumatoid arthritis and spondyloarthritis. Over 14 days, 50 participants answered short surveys on their phone and wore a device to track movement. The goal was to see how fatigue, pain, mood, and sleep affect physical activity in real time, and to refine methods for future larger studies.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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50 people
The number who actually took part.
- Started
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Nov 2025
- Finished
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Apr 2026
- 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
Adults diagnosed with Chronic inflammatory rheumatic diseases (rheumatoid arthritis or spondyloarthritis)
- 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: * Adults (≥18 years) with a confirmed diagnosis of CIRDs, including RA or SpA, established by a rheumatologist, are eligible for inclusion. * Adults able to understand and consent to the study protocol, * Adults affiliated with a social security system * Adults that have access to a digital device with internet access (e.g., smartphone or tablet). Non-inclusion Criteria: * Insufficient proficiency in the French language * Legal incapacity or deprivation of liberty * Major cognitive impairment incompatible with repeated questionnaire completion (e.g., Alzheimer's disease) * Pregnant or breastfeeding women * Individuals with a history of alcohol or substance abuse, or severe psychiatric disorders that could affect adherence to the protocol or the reliability of collected data, are also excluded.
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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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CHU Grenoble Alpes
Grenoble, France, 38000, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.