Rheumatoid Arthritis, Telehealth
Conditions
Keywords
Rheumatoid Arthritis
Brief summary
The COVID-19 outbreak has affected health care of patients with rheumatic diseases; telemedicine might help to assist patients. The primary objective is to determine if a hybrid medical care model, which consists of alternating face-to-face medical visits and video medical consultations, is not inferior, in terms of the Patient Reported Outcomes measures (PROMs), to the face-to-face medical care model, among rheumatoid arthritis (RA) outpatients. We also aim to investigate if adherence to RA-related treatment (considered a surrogate of patient´s education) might be improved when patients are re-integrated to the health care system, irrespective of the health care model. In Mexico, COVID-19 pandemic still uncontrolled. Our Institution provides health care to 1500 RA patients/year and up to August 2020, it is estimated that 500 RA patients might be affected, which is our target audience. Reinstalling institutional health care provision is challenging. This a non-inferiority, cross-over study, with 2 intervention arms. Patients will be randomized to 1. Six months of usual medical care model, followed by 4 months of a control period, and 6 months of hybrid medical care model, or 2. Six months of hybrid medical care model, followed by 4 months of a control period, and 6 months of usual medical care model. The following PROMs will be assessed at specific time points: disease activity/disease severity (RAPID-3), disability (HAQ-DI), quality of life (WHOQOL-BREF), patient satisfaction with the medical care model (questionnaire locally developed), patient´s adherence to medical care (missed scheduled visits) and patient´s adherence to RA-related treatment (the Compliance-Questionnaire).
Detailed description
This a non-inferiority and cross-over study, with a planned follow-up of 16 months, with 2 intervention arms: Intervention 1: Patients assigned to 6 months of usual medical care model, followed by 4 months control period, and finally 6 months of hybrid medical care model. Intervention 2: Patients assigned to 6 months of hybrid medical care model, followed by 4 months control period and finally 6 months of usual medical care model. Specific objectives are as follows: Primary objectives 1. To compare the mean disease activity of RA patients (as measured per RAPID-3), after 6 months since study entry, between patients assigned to intervention 1 and patients assigned to intervention 2. 2. To compare the RA patient´s quality of life (as measured per WHOQOL-BREF) and RA patient's disability (as measured per HAQ-DI) after 6 months since study entry, between patients assigned to intervention 1 and patients assigned to intervention 2. Secondary objectives: 1. At the end of the complete follow-up period, for each patient, to compare the cumulative RA disease activity during the 6 months period where patients received usual medical care model, with the cumulative disease activity during the 6 months period where patients received hybrid medical care model. 2. At the end of the complete follow-up period, for each patient, to compare patient´s satisfaction with usual medical care model and patient´s satisfaction to hybrid medical care model. 3. At the end of the complete follow-up period, for each patient, to compare patient´s adherence to the usual medical care model with patient´s adherence to hybrid medical care model.
Interventions
Face-to-face medical visits
Alternating face-to-face medical visits and video medical consultations
Sponsors
Study design
Intervention model description
This a non-inferiority and cross-over study, with a planned follow-up of 16 months, with 2 intervention arms: Intervention 1: Patients assigned to 6 months of usual medical care model, followed by 4 months of a control period, and finally 6 months of hybrid medical care model. Intervention 2: Patients assigned to 6 months of hybrid medical care model, followed by 4 months of a control period, and finally 6 months of usual medical care model.
Eligibility
Inclusion criteria
* Patients with RA diagnosis according to their primary rheumatologist * With at least six months of follow-up (up to March 2020) at the outpatient clinic * Who agree to participate
Exclusion criteria
* Patients lost to follow-up from the outpatient clinic before March 2020 * Patients with no access to a mobile device during their study participation * Patients with severe cognitive, visual and hearing impairment * Patients on palliative care because of comorbid condition
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Rheumatoid arthritis patient´s disease activity | During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models) | The disease activity measured by a RAPID-3 instrument |
| Rheumatoid arthritis patient´s quality of life | During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models) | Quality of life measured by a WHOQOL-BREF instrument |
| Rheumatoid arthritis patient's disability | During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models) | Disability measured by a HAQ-DI instrument |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Satisfaction with medical care | During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models) | Questionnaire locally developed |
| Patient´s adherence to medical care | During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models) | Number of missed scheduled visits |
Countries
Mexico