- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04768413
Evaluation of a Non-face to Face Multidisciplinary Health Care Model in a Population With Rheumatoid Arthritis
Evaluation of a Non-face to Face Multidisciplinary Health Care Model in a Population With Rheumatoid Arthritis Highly Vulnerable to the 2019 Novel Coronavirus Disease
Study Overview
Status
Conditions
Detailed Description
The evaluation of the priority implementation of a non-face-to-face multidisciplinary health care model is justified in a population highly vulnerable to COVID 19, with Rheumatoid arthritis (RA) in a health emergency situation and in turn seeking to promote its well-being, taking into account the importance of interdisciplinary follow-up to strengthen self-care, avoid deterioration, hospital admissions and improve therapeutic adherence. This research work proposes the evaluation of the implementation of a tele-orientation program and tele-consultation to the adult population with RA attended at a specialized rheumatology center in Bogota, Colombia, over a period of three months, by means of a observational, analytical, cohort, prospective study that will include mixed methods for collecting information (quantitative and qualitative). The qualitative methods will include interviews with a subgroup of patients attending by the two models and with the professionals who care for them, with the aim of knowing the experiences and perceptions of both the patients and the professionals.
The impact that the project seeks is focused on evaluating the program's contribution to the control of RA symptoms and inflammation, avoiding progressive structural damage.
On the other hand, elements will be provided to advance towards telehealth educational interventions and their effect in improving the therapeutic adherence of patients with RA, as well as avoiding their displacement, maintaining quarantine measures and stimulating necessary self-care measures in search of mitigate the COVID-19 pandemic and counteract the spread of the severe acute respiratory syndrome coronavirus 2, particularly in this susceptible risk group.
Finally, this study will provide information on the characteristics of RA patients who choose telemedicine compared to face-to-face care when both are offered as usual care options during an unprecedented situation such as the COVID-19 pandemic. For this reason, the possibility of replication at the national level from the planning of telemedicine programs in rheumatology will be essential for contributing to the reduction of epidemiological indicators against contagion by coronavirus and the use of hospital service
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Pedro Santos Moreno, MD: Rhe
- Phone Number: +573208094232
- Email: pedrivansamo@hotmail.com
Study Contact Backup
- Name: Adriana Rojas -Villarraga, MD; Rhe
- Phone Number: +573187117073
- Email: sarojas@fucsalud.edu.co
Study Locations
-
-
Cundinamarca
-
Bogota, Cundinamarca, Colombia, 250017
- Recruiting
- BIOMAP IPS Centro de Atención Integral en Artritis Reumatoide
-
Contact:
- PEDRO SANTOS - MORENO, MD;Rhe
- Phone Number: +573208094232
- Email: pedrivansamo@hotmail.com
-
Contact:
- ADRIANA ROJAS-VILLARRAGA, MD;Rhe
- Phone Number: +573187117073
- Email: sarojas@fucsalud.edu.co
-
Bogota, Cundinamarca, Colombia, 250017
- Recruiting
- Colombia Fundación Universitaria de Ciencias de la Salud-FUCS
-
Contact:
- ADRIANA ROJAS-VILLARRAGA, MD;Rhe
- Phone Number: +573187117073
- Email: sarojas@fucsalud.edu.co
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Quantitative and qualitative approach. Patients over 18 years of age with confirmed diagnosis of rheumatoid arthritis International Classification of Diseases: M069, M059, M060, treated at a reference center for these pathologies in the city of Bogotá.
- Quantitative approach Patients with access to information and communication technologies
- Qualitative approach: Patients seen in the teleconsultation modality on at least two occasions.
- Qualitative approach: Patients attended in the face-to-face consultation modality on at least two occasions.
- Qualitative approach: Health professionals who have carried out at least 25 teleconsultations directed at patients with rheumatoid arthritis in a reference center for these pathologies in the city of Bogotá.
Exclusion Criteria:
- Patients who due to their cognitive conditions do not have the ability to provide reliable information necessary for the development of the study.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Group A
A group of patients who have voluntarily adhered to the clinic's tele-assisted consultation and who receive remote, multidisciplinary team care without requiring physical displacement.
|
A group of patients who have voluntarily adhered to the clinic's tele-assisted consultation and who receive remote, multidisciplinary team care without requiring physical displacement.
|
Group B
Group of patients who wish to continue with the usual face-to-face consultation, since for these patient's isolation measures allow trips to the care centers and who receive care from a multidisciplinary team on a regular basis.
|
Group of patients who wish to continue with the usual face-to-face consultation, since for these patient's isolation measures allow trips to the care centers and who receive care from a multidisciplinary team on a regular basis.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Evaluation of the implementation of a non-face-to-face multidisciplinary consultation model in a population of rheumatoid arthritis
Time Frame: up to Week 12
|
Evaluate the implementation of a non-face-to-face multidisciplinary consultation model in a population with rheumatoid arthritis, highly vulnerable to severe acute respiratory syndrome coronavirus 2 [coronavirus disease (COVID-19)] during a health emergency situation and evaluation of the effectiveness of their results.
|
up to Week 12
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Epidemiological characterization
Time Frame: up to Week 12
|
Epidemiological characterization of the population evaluated under the multidisciplinary health care model, both in teleconsultation and face-to-face consultation.
|
up to Week 12
|
Proportion of individuals infected
Time Frame: up to Week 12
|
To determine the proportion of individuals infected with severe acute respiratory syndrome coronavirus 2 [coronavirus disease (COVID-19)] in those patients who regularly receive different immunosuppressive medications under the two care models (teleconsultation and face-to-face).
|
up to Week 12
|
Risk factors for infection
Time Frame: up to Week 12
|
Describe the risk factors for severe acute respiratory syndrome coronavirus 2 [coronavirus disease (COVID-19)] infection in the group of patients linked to the teleconsultation model and in those with regular face-to-face care.
|
up to Week 12
|
Risk factors for hospitalization
Time Frame: up to Week 12
|
Describe the risk factors for hospitalization associated with severe acute respiratory syndrome coronavirus 2 [coronavirus disease (COVID-19)] in the group of patients linked to the teleconsultation model and in those with regular face-to-face care.
|
up to Week 12
|
Risk factors for mortality
Time Frame: up to Week 12
|
Describe the risk factors for mortality associated with severe acute respiratory syndrome coronavirus 2 [coronavirus disease (COVID-19)] in the group of patients linked to the teleconsultation model and in those with regular face-to-face care.
|
up to Week 12
|
Average change from baseline in Disease Activity Score with 28-joint counts [DAS28] in face-to-face consultation group
Time Frame: up to Week 12
|
A single score on a continuous scale (0-9.4).
The level of disease activity will be interpreted as remission (DAS28 <2.6), low (2.6 ≤ DAS28 < 3.2), moderate (3.2 ≤DAS28≤ 5.1), or high (DAS28 >5.1).
|
up to Week 12
|
Average change from baseline in Patient Activity Scale scores in both groups tele-assisted consultation and face-to-face consultation
Time Frame: up to Week 12
|
The Patient Activity Scale is calculated by multiplying the Health Assessment Questionnaire (HAQ) by 3.33 and then dividing the sum of the visual analogue scale (VAS) pain, Patient global assessment (PtGA), and Health Assessment Questionnaire (HAQ) by 3. Activity will be interpreted as these categories of disease activity: remission ≤0.25, low ≤3.7, moderate <8.0, and high ≥8.0.
|
up to Week 12
|
Evaluation of participant's pain using visual analogue scale [VAS] in both groups tele-assisted consultation and face-to-face consultation
Time Frame: Baseline, Week 6 and 12
|
Paint measurement for any disease state 0-10 centimeters VAS by the patient
|
Baseline, Week 6 and 12
|
Evaluation of the disease activity by Doctor using visual analogue scale [VAS] in both groups tele-assisted consultation and face-to-face consultation
Time Frame: Baseline, Week 6 and 12
|
Activity measurement for any disease state 0-10 centimeters VAS by the Doctor
|
Baseline, Week 6 and 12
|
Absolute and percent change in the Health Assessment Questionnaire (HAQ) in both groups tele-assisted consultation and face-to-face consultation
Time Frame: Baseline, Week 6 and 12
|
The questionary includes 20 daily life questions, grouped in 8 areas, each one containing two or three questions related to daily life activities.
Each question is scored from 0-3. 0 means no disability, 3 score means completely disabled.
The average of all responses is done.
Average scores from 0-1 represent "mild to moderate difficulty", 1-2 means "moderate to severe disability", 3-2 indicates "severe to very severe disability".
|
Baseline, Week 6 and 12
|
Average change from baseline in European Quality of Life 5 Dimensions (EQ-5D) questionnaire in both groups tele-assisted consultation and face-to-face consultation
Time Frame: up to Week 12
|
European Quality of Life 5 Dimensions (EQ-5D) questionnaire is a self-reported health outcome which measures Quality of life (QoL) in five dimensions.
An overall score is derived that measures from the least (worst) to the highest score (best).
In addition, health state is measured on the vertical Visual Analogue scale (score 0 to 100) with higher scores (better health status).
|
up to Week 12
|
Evaluation of the level of therapeutic adherence using a specific Scale in both groups tele-assisted consultation and face-to-face consultation
Time Frame: Baseline and week 12.
|
The four item MORISKY-GREEN-LEVINE Medication Adherence Scale (MGLS) results in a score ranging from 0 to 4. There are three levels of medication adherence based on this score: high, medium and low adherence with 0, 1-2, and 3-4 points, respectively.
A dichotomous definition of adherence based on MGLS will be used with 0 points indicating perfect adherence and 1+ points indicating some level of non-adherence.
|
Baseline and week 12.
|
Evaluation of the self-care capacity using the Appraisal of Self-care Agency Scale -Revised (ASA-R) in both groups tele-assisted consultation and face-to-face consultation
Time Frame: Baseline and week 12.
|
The Appraisal of Self-care Agency Scale -Revised (ASA-R; Sousa et al.) is one of the main instruments to assess self-care capacity.
It consists of a total of 15 questions in 3 areas, of which the area lacking self-care agency is reversely coded.
Based on a 5-point Likert scale, a higher total score signified a higher level of self-care agency.
|
Baseline and week 12.
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Description of individual experiences of patients: Qualitative data analysis
Time Frame: The moment of the interview (week 12)
|
A semi-directed interview will be undertaken with patients with rheumatoid arthritis.
The aim will be to obtain a description of their experiences concerning how their health care was developed during the pandemic time and how health-related decisions are made individually considering the interactions with health care professionals in both models face to face and teleconsultation.
|
The moment of the interview (week 12)
|
Description of individual experiences of health care professionals: Qualitative data analysis
Time Frame: The moment of the interview (week 12)
|
Health care professionals will also be interviewed regarding their experiences and needs in rheumatoid arthritis attention based on the two models, in the shared decision-making process and in establishing objective medical decisions.
|
The moment of the interview (week 12)
|
Collaborators and Investigators
Investigators
- Principal Investigator: Adriana Rojas-Villarraga, MD;Rhe, Fundación Universitaria de Ciencias de la Salud
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 5171
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Rheumatoid Arthritis
-
Janssen Research & Development, LLCWithdrawnActive Rheumatoid Arthritis; Rheumatoid Arthritis
-
Centocor, Inc.CompletedRheumatoid Arthritis, Juvenile
-
AmgenTerminated
-
Children's Hospital Medical Center, CincinnatiNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)CompletedJuvenile Rheumatoid ArthritisUnited States
-
AmgenImmunex CorporationCompletedJuvenile Rheumatoid Arthritis
-
National Institute of Arthritis and Musculoskeletal...Children's Hospital Medical Center, CincinnatiCompleted
-
University of PittsburghNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)CompletedRheumatoid Arthritis | Juvenile Rheumatoid ArthritisUnited States
-
University of Missouri-ColumbiaCompletedJuvenile Rheumatoid ArthritisUnited States
-
Assistance Publique - Hôpitaux de ParisSociete Francaise de RhumatologieRecruiting
-
Amsterdam UMC, location VUmcEuropean CommissionCompletedRheumatoId ArthritisNetherlands, Germany, Portugal, Italy, Hungary, Romania, Slovakia
Clinical Trials on Teleconsultation either by phone or by computer consultation. Quantitative and qualitative approaches to analysis
-
University Hospital, Strasbourg, FranceCompletedDiabetes | Covid-19France
-
Memorial Sloan Kettering Cancer CenterCompletedKidney Cancer | Renal CancerUnited States
-
Memorial Sloan Kettering Cancer CenterCompletedThyroid Cancer | Papillary MicrocarcinomaUnited States