Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06742385

Evaluation of a Remote Monitoring Application in the Follow-up of Patients With Active Inflammatory Bowel Diseases

Led by Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives · Updated on 2025-09-24

290

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

Sponsors

G

Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives

Lead Sponsor

A

AbbVie

Collaborating Sponsor

AI-Summary

What this Trial Is About

Telemonitoring is of definite theoretical interest for patients suffering from chronic diseases and could help to improve monitoring of treatment efficacy and tolerance, and hence remission and quality of life. Reimbursement is now planned in France for devices that have demonstrated a positive effect on patient intake. However, available studies testing different tools in IBD have shown no significant improvement in disease control or quality of life. Nevertheless, major secondary endpoints such as reduced hospitalization, complications and healthcare costs have been demonstrated. Several biases have been identified to explain these disappointing results, such as the heterogeneity of the tools/applications tested, methodological limitations concerning the main objective and technological limitations of the tools evaluated. We propose here to evaluate the impact of a tight remote monitoring through digital tool on disease control, in patients with active IBD, thanks to the MedicWise platform. The technology of the MedicWise solution enables the automatic collection of a wide range of biological and healthcare consumption data, thus limiting the need for patient input. MedicWise has obtained the CE label and is already used and reimbursed in France in other chronic diseases. The SECURITY trial proposes to evaluate the impact of a tight remote monitoring through digital tool on time spent in remission. Improvement of IBD related disability is also a major secondary objective of the study. It also has the following secondary objectives to analyze the impact of this tool on the organization of care teams caring for patients with IBD.

CONDITIONS

Official Title

Evaluation of a Remote Monitoring Application in the Follow-up of Patients With Active Inflammatory Bowel Diseases

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of Crohn Disease or Ulcerative Colitis
  • Age above 18 years and up to 80 years
  • Active IBD with clinical signs requiring medical treatment change such as new treatment, dose change, or addition of corticosteroids, ASA, immunosuppressants, or biotherapy (4-week induction phase allowed)
  • Willing and able to participate using the SEMEIA smartphone app
  • Agree to participate in the study for 12 months
Not Eligible

You will not qualify if you...

  • Unable to use a smartphone or email
  • Under 18 years of age
  • Scheduled digestive surgery within 3 months
  • Pregnant at the start of the study
  • History of sub-total colectomy, coloproctectomy, digestive ostomy, or extensive intestinal resections causing diarrhea or short bowel syndrome
  • Recent digestive surgery (ileal resection less than 6 months ago)
  • Uncontrolled other physical or psychiatric illnesses
  • Currently enrolled in a trial with investigational treatment

AI-Screening

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Trial Site Locations

Total: 1 location

1

Institut des MICI

Neuilly-sur-Seine, France, France, 92200

Actively Recruiting

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Research Team

X

Xavier TRETON, Pr

CONTACT

G

GETAID GETAID

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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