Evaluation of the Use of an E-health Therapeutic Education Application for Osteoarthritis Patients
NCT ID: NCT04750304
Last Updated: 2022-07-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
32 participants
OBSERVATIONAL
2022-01-31
2022-07-07
Brief Summary
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The recommendations of recent years favor the non-pharmacological treatment of osteoarthritis including regular physical activity, therapeutic education and weight loss Osteoarthritis population has a low level of physical activity due to a lack of information, motivation and false beliefs related to physical activity and kinesiophobia (fear of movement) A preliminary qualitative study (ARTHe1) evaluating the barriers and levers of the use of an e-health therapeutic education application in patients with osteoarthritis was carried out in order to guide the development of the ARTHe application.
The objective of this study is to have the application tested on a panel of patients in order to assess the benefits of using the application in terms of adherence to the practice of physical activity but also in clinical terms on function and pain, and the satisfaction of the patient
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Detailed Description
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Patient recruitment will be done in the PRM department of Clermont-Ferrand University Hospital A subgroup of patients will receive a Garmin VivoSmart 4 connected wristband, which will record intrinsic stress measurement data during the test.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Application ARTHe
Patient will use ARTHe Application for 3 months
Eligibility Criteria
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Inclusion Criteria
* Patients with osteoarthritis according to the ACR (American College of Rheumatology) criteria, symptomatic and diagnosed before inclusion by a specialist or not.
* Patients with least one knee impairment
* Patients with a smartphone or tablet with at least Android 5 or iOS 11.
* Volunteer patients willing to participate in the study.
Exclusion Criteria
* Patients with comprehension disorders making it impossible to interview and complete questionnaires or use the application.
* Refusal to participate or being already included in a research protocol that could influence the current protocol.
* Patients under guardianship, curatorship or deprived of liberty.
18 Years
ALL
No
Sponsors
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Openium
UNKNOWN
Caleden
UNKNOWN
Innovatherm
INDUSTRY
BPIfrance
OTHER
University Hospital, Clermont-Ferrand
OTHER
Responsible Party
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Locations
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Clermont-Ferrand University Hospital
Clermont-Ferrand, AURA, France
Countries
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Other Identifiers
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RNI 2020 COUDEYRE
Identifier Type: -
Identifier Source: org_study_id
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