Impact of a Hybrid Medical Care Model in the Rheumatoid Arthritis Patient-reported-outcomes Measures
Primary Purpose
Rheumatoid Arthritis, Telehealth
Status
Completed
Phase
Not Applicable
Locations
Mexico
Study Type
Interventional
Intervention
Face-to-face medical visits
Alternating face-to-face medical visits and video medical consultations
Sponsored by
About this trial
This is an interventional health services research trial for Rheumatoid Arthritis focused on measuring Rheumatoid Arthritis
Eligibility Criteria
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
Sites / Locations
- Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Usual Medical Care Model
Hybrid Medical Care Model
Arm Description
All the patients will receive face-to-face medical visits
The patients will receive alternating face-to-face medical visits and video medical consultations
Outcomes
Primary Outcome Measures
Rheumatoid arthritis patient´s disease activity
The disease activity measured by a RAPID-3 instrument
Rheumatoid arthritis patient´s quality of life
Quality of life measured by a WHOQOL-BREF instrument
Rheumatoid arthritis patient's disability
Disability measured by a HAQ-DI instrument
Secondary Outcome Measures
Satisfaction with medical care
Questionnaire locally developed
Patient´s adherence to medical care
Number of missed scheduled visits
Full Information
NCT ID
NCT04558905
First Posted
September 10, 2020
Last Updated
September 26, 2022
Sponsor
National Institute of Medical Sciences and Nutrition, Salvador Zubiran
1. Study Identification
Unique Protocol Identification Number
NCT04558905
Brief Title
Impact of a Hybrid Medical Care Model in the Rheumatoid Arthritis Patient-reported-outcomes Measures
Official Title
Impact of a Hybrid Medical Care Model (Face-to-face Medical Visits Alternating With Video Medical Consultations) in the Rheumatoid Arthritis Patient-reported-outcomes Measures: A Non-inferiority Study
Study Type
Interventional
2. Study Status
Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
October 1, 2020 (Actual)
Primary Completion Date
April 1, 2022 (Actual)
Study Completion Date
May 31, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Institute of Medical Sciences and Nutrition, Salvador Zubiran
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
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
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.
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:
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.
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.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rheumatoid Arthritis, Telehealth
Keywords
Rheumatoid Arthritis
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
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.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
156 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Usual Medical Care Model
Arm Type
Active Comparator
Arm Description
All the patients will receive face-to-face medical visits
Arm Title
Hybrid Medical Care Model
Arm Type
Experimental
Arm Description
The patients will receive alternating face-to-face medical visits and video medical consultations
Intervention Type
Other
Intervention Name(s)
Face-to-face medical visits
Intervention Description
Face-to-face medical visits
Intervention Type
Other
Intervention Name(s)
Alternating face-to-face medical visits and video medical consultations
Intervention Description
Alternating face-to-face medical visits and video medical consultations
Primary Outcome Measure Information:
Title
Rheumatoid arthritis patient´s disease activity
Description
The disease activity measured by a RAPID-3 instrument
Time Frame
During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models)
Title
Rheumatoid arthritis patient´s quality of life
Description
Quality of life measured by a WHOQOL-BREF instrument
Time Frame
During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models)
Title
Rheumatoid arthritis patient's disability
Description
Disability measured by a HAQ-DI instrument
Time Frame
During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models)
Secondary Outcome Measure Information:
Title
Satisfaction with medical care
Description
Questionnaire locally developed
Time Frame
During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models)
Title
Patient´s adherence to medical care
Description
Number of missed scheduled visits
Time Frame
During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Virginia Pascual-Ramos, Dr.
Organizational Affiliation
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
Official's Role
Principal Investigator
Facility Information:
Facility Name
Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán
City
Mexico City
State/Province
Tlalpan
ZIP/Postal Code
14080
Country
Mexico
12. IPD Sharing Statement
Plan to Share IPD
No
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Impact of a Hybrid Medical Care Model in the Rheumatoid Arthritis Patient-reported-outcomes Measures
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