Evaluation of the Use of an E-health Therapeutic Education Application for Osteoarthritis Patients

NCT ID: NCT04750304

Last Updated: 2022-07-11

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

32 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-01-31

Study Completion Date

2022-07-07

Brief Summary

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Osteoarthritis is the most common joint disease affecting the joint in a comprehensive and progressive manner. It leads to increasing disability.

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

Detailed Description

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This is a prospective observational study including the evaluation of the use of the ARTH-e application after 3 weeks, 6 weeks and 3 months of use.

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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Osteo Arthritis Knee

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Application ARTHe

Patient will use ARTHe Application for 3 months

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Patients older than 18 years
* 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 no diagnostic criteria for ACR.
* 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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Openium

UNKNOWN

Sponsor Role collaborator

Caleden

UNKNOWN

Sponsor Role collaborator

Innovatherm

INDUSTRY

Sponsor Role collaborator

BPIfrance

OTHER

Sponsor Role collaborator

University Hospital, Clermont-Ferrand

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Clermont-Ferrand University Hospital

Clermont-Ferrand, AURA, France

Site Status

Countries

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France

Other Identifiers

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RNI 2020 COUDEYRE

Identifier Type: -

Identifier Source: org_study_id

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