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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06273306
Other study ID # HULP.PI-4519
Secondary ID PI22/00777
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 15, 2024
Est. completion date December 31, 2026

Study information

Verified date December 2023
Source Instituto de Investigación Hospital Universitario La Paz
Contact Chamaida Plasencia-Rodríguez, PhD
Phone 917277108
Email chamiplaro@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main objective is to evaluate the implementation of a hybrid care model called the mixed attention model (MAM) in clinical practice and to evaluate whether its implementation improves clinical outcomes compared to conventional follow-up. This is a multicenter prospective observational study involving 360 patients with rheumatoid arthritis (RA) and Spondylarthritis (SpA) from five Spanish Hospitals. Patients will be followed-up by the MAM protocol, which is a care model that incorporates the use of digital tool consisting of a mobile application (App) that patients can use at home and that professionals can review asynchronously to detect incidents and to follow their patients; clinical evolution between face-to-face visits. Another group of patients, whose follow-up will be conducted in accordance with a traditional face-to-face care model, will be assessed as the control group. Sociodemographic characteristics, treatments, laboratory parameters, assessment of tender and swollen joints, visual analogue scale for pain and electronic patient reported outcome reports (ePROs) will be collected for all subjects. In the MAM group, these items will be self-assessed both by the mobile App and during face-to-face visits with rheumatologist, who will do the same for patients included in the traditional care model. Patients will be able to report any incidence related to their disease or treatment through the mobile App.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 360
Est. completion date December 31, 2026
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Clinical diagnosis with Rheumatoid Arthritis or Spondylarthritis - Treatment with biologic or targeted disease modifying antirheumatic drugs. - Ability to use smartphone. Exclusion Criteria: - only patients with conditions that hinder or prevent the use of a mobile application (blindness, mental retardation, dementia, digitalfilliteracy).

Study Design


Intervention

Device:
IMIDOC
Patient´s Mobile App for recording clinical data

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Instituto de Investigación Hospital Universitario La Paz

Outcome

Type Measure Description Time frame Safety issue
Primary To assess the primary objective, composite endpoints that consider the viability, adherence and degree of satisfaction of the MAM are included Number of interactions in activity and electronic patient reported outcomes (ePRO) questionnaires per month.
Number of reported incidences per month.
Average time to contact the patient after reporting an incident.
Average number of interactions in educational material and other content per month.
Adherence to follow-up through the mixed atenttion model (MAM) will be evaluated through the number of visits and time per visit to the digital platform.
Percentage of incidents resolved telematically.
Average weekly hours that the digital clinician takes to review the professional's website and resolve incidents
Professionals and patients´ satisfaction will be assessed through the Net-Promoter-Score (NPS). Values from 0 to 6 ( detractors), 6-8 ( passives) and 9-10 promoters.
24 months
Secondary To identify features associated with adherence to follow-up through the MAM. A 22-item self-administered survey adapted from the Unified Theory of Acceptance and Use of Technology (UTAUT) model will be used to measure app acceptance and intention to use: the variables will measured with 7-point scales for all model components as in the original UTAUT, where 1 equalled the negative end (fully disagree) and 7 the positive end of the scale (fully agree).
Agreement between patients' self-assessment and clinician assessment will be assessed comparing face-to-face visits at 6-months intervals with the closest assessment in the digital solution.
Number of face-to-face visits are avoided with the mixed atenttion model (MAM) in patients with stable disease activity.
Patients' eHealth literacy will be measured using the validated Spanish version of the eHealth Literacy Scale (eHEALS), measured on a 5-point scale in the range from 1 (strongly disagree) to 5 (strongly agree)
24 months
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