NCT06742385Recruiting
Evaluation of a Remote Monitoring Application in the Follow-up of Patients With Active Inflammatory Bowel Diseases
Evaluation of a Remote Monitoring Application in the Follow-up of Patients With Active Inflammatory Bowel Diseases: The SECURITY Trial
Source: ClinicalTrials.gov · Last updated 24 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 290 (estimated)
- First submitted
- 16 Dec 2024
- Start date
- 18 Sept 2025
- Primary completion date
- 18 Sept 2027
- Lead sponsor
- Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives
- Diseases
- Crohn's disease, Ulcerative colitis
- NCT number
- NCT06742385
What you commit to
- Study type: Interventional
- Planned participants: 290
- From 18 Sept 2025 to the primary completion date, 18 Sept 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Digestive surgery expected within 3 months
Other illness
- Patients with an history of sub-total colectomy, coloproctectomy, digestive ostomy, extensive or multiple intestinal resections with sequelae of diarrhoea, short bowel syndrome.
- Patients who have had recent digestive surgery (ileal resection \< 6 months) Patients with any other uncontrolled somatic or psychiatric pathology
Age
- Patients \< 18 years old
Other
- Patients with an inability to use a smartphone and email
- Pregnancy at baseline
- Patients enrolled in a trial with an investigational treatment
Who the study is looking for
- CD/UC patients with a validated diagnosis
- Patients age \> 18 years
- IBD with clinical signs of PRO2 activity leading to modification of medical treatment: introduction of a new treatment, or change of dose or addition of a treatment (corticoids, ASA, IS, biotherapy (a 4 week induction phase is authorized
- Patients willing and able to participate in the collection of data via SEMEIA App on their smartphone
- Patients agreeing to participate for 12 months
Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Institut des MICI Coordinator of this site? Confirm its status | Neuilly-sur-Seine | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.