Impact of Telemonitoring in the Management of Complex IBD in Spain: M-TECCU (M-TECCU)
Inflammatory Bowel Disease, Crohn's Disease, Ulcerative Colitis
About this trial
This is an interventional other trial for Inflammatory Bowel Disease
Eligibility Criteria
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
Sites / Locations
- Hospital Universitario y Politécnico la Fe
Arms of the Study
Arm 1
Arm 2
No Intervention
Active Comparator
control group
TECCU group