Impact of Telemonitoring in the Management of Complex IBD in Spain: M-TECCU

Sponsor
Grupo Espanol de Trabajo en Enfermedad de Crohn y Colitis Ulcerosa (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT06031038
Collaborator
(none)
290
1
2
46
6.3

Study Details

Study Description

Brief Summary

M-TECCU is a study: multicenter, randomized and open. It consists of two parallel groups to compare the efficacy of the TECCU web-based telemonitoring system to achieve and maintain activity remission in patients with moderate-high complexity inflammatory bowel disease compared to usual clinical practice.

Condition or Disease Intervention/Treatment Phase
  • Other: TECCU Software
N/A

Detailed Description

Clinical trial with an open, randomized and controlled non-inferiority medical device, in which the impact of a follow-up method through a web telemonitoring platform on the time in clinical remission of patients with complex IBD is evaluated, in comparison with the usual follow-up in outpatient clinics.

Patients with complex IBD are considered to be those who receive treatment with immunosuppressants or biological therapies to control the luminal activity of their disease. Patients carry out periodic controls for the disease according to a pre-established schedule based on national and international clinical guidelines. The patients in the telemonitoring group (G_TECCU) follow these controls through the TECCU platform, a web system that allows them to fill in questionnaires related to the clinical variables under study and communicate freely with healthcare personnel during pre-established controls and when the patient deems it necessary. On the other hand, the patients of the control group (G_Control) carry out the controls according to the same schedule as G_TECCU, but following the usual clinical practice.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
290 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
To compare the time in remission of patients with complex IBD (require immunosuppressants and/or biologics to control their luminal inflammatory activity) controlled with the TECCU intervention (G_TECCU) with respect to usual clinical practice (G_Control) after 52 weeks of follow-up.To compare the time in remission of patients with complex IBD (require immunosuppressants and/or biologics to control their luminal inflammatory activity) controlled with the TECCU intervention (G_TECCU) with respect to usual clinical practice (G_Control) after 52 weeks of follow-up.
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Impact of Telemonitoring in the Management of Complex Inflammatory Bowel Disease in Spain: TECCU Multicenter Study
Actual Study Start Date :
Jul 1, 2020
Actual Primary Completion Date :
Apr 30, 2023
Anticipated Study Completion Date :
Apr 30, 2024

Arms and Interventions

Arm Intervention/Treatment
No Intervention: control group

Active Comparator: TECCU group

Other: TECCU Software
patient monitoring by software application

Outcome Measures

Primary Outcome Measures

  1. clinical remission [52 weeks]

    To compare the time in remission of patients with complex IBD (require immunosuppressants and/or biologics to control their luminal inflammatory activity) controlled with the TECCU intervention (G_TECCU) with respect to usual clinical practice (G_Control) after 52 weeks of follow-up.

Secondary Outcome Measures

  1. cost-effectiveness [52 weeks]

    Carry out a cost-effectiveness analysis based on the direct and indirect costs generated during the 12-month follow-up in G_TECCU and G_control.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients ≥18a

  • IBD (CD or UC) diagnosed according to ECCO criteria

  • Start treatment with immunosuppressants and/or biological therapies due to luminal activity

  • signed informed consent

Exclusion Criteria:
  • Pregnant women

  • Presence of active perianal disease, ileoanal reservoir, or definitive stoma

  • Patients with mental illness or other poorly controlled illness

  • Patients with active cancer diagnosis

  • Terminal patients and/or palliative care (SECPAL)

  • Family members of the research team

  • Patients without a telephone line to connect with a mobile, tablet and/or computer / Inability to drive

  • Cognitive or linguistic difficulties

  • Patients included in another experimental study

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital Universitario y Politécnico la Fe Valencia Spain 46026

Sponsors and Collaborators

  • Grupo Espanol de Trabajo en Enfermedad de Crohn y Colitis Ulcerosa

Investigators

  • Principal Investigator: Castany Pla, Spanish Working Group on Crohn's disease and ulcerative colitis (GETECCU)

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Grupo Espanol de Trabajo en Enfermedad de Crohn y Colitis Ulcerosa
ClinicalTrials.gov Identifier:
NCT06031038
Other Study ID Numbers:
  • M-TECCU
First Posted:
Sep 11, 2023
Last Update Posted:
Sep 11, 2023
Last Verified:
Jul 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 11, 2023