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Mobile application based follow-up and rehabilitation in rheumatoid arthritis patients compared with conventional followup

My Ra Journey Novel App for Follow-up and Rehabilitation of Patients with Rheumatoid Arthritis and Comparison of the Incidence of Complications in Patients Using the Application and Patients on Conventional Follow-up - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/107223
Enrollment
100
Registered
2026-04-01
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M00-M99- Diseases of the musculoskeletal system and connective tissue

Interventions

Intervention1: App based monitoring,rehabilitation,followup: Total duration of intervention is 6months.The intervention in this study consists of the use of the My RA Journey mobile application, a d

Sponsors

Saveetha Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age more than or equal to 18 years 2.Diagnosed Rheumatoid Arthritis 3.Under regular follow-up 4.Owns smartphone 5.Able to use mobile application 6.Willing to provide informed consent

Exclusion criteria

Exclusion criteria: 1.Cognitive impairment 2.Severe visual/motor disability 3.No smartphone access 4.Participation in another clinical trial 5.Severe psychiatric illness 6.Pregnant/lactating women

Design outcomes

Primary

MeasureTime frame
The primary outcome of this study is the incidence of rheumatoid arthritis related complications during the study period, including disease flares, joint deformities, unplanned hospital visits, and worsening functional status. This will be assessed by comparing the frequency of such complications between patients using the My RA Journey mobile application and those receiving conventional follow-up care over the defined follow-up period. Timepoint: outcomes will be assessed at baseline and every 4weeks for total duration of 6months i.e at baseline, 4th week,8th week,12th week,16th week till 6months—

Secondary

MeasureTime frame
Secondary outcomes include evaluation of changes in disease activity scores (such as DAS28 or CDAI), treatment & physiotherapy adherence, patient satisfaction & engagement, & quality of life measures. Additional secondary outcomes include reduction in missed follow-up visits, improved medication compliance, & decreased frequency of emergency visits, measured periodically during the study duration.Timepoint: outcomes will be assessed at baseline & every 4weeks for total duration of 6months i.e at baseline, 4th week,8th week,12th week,16th week till 6months—

Countries

India

Contacts

Public ContactAnanthakumar PK

Saveetha Medical College and Hospital

ananthakumarpk@gmail.com9620916481

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026