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

Primary Purpose

Inflammatory Bowel Disease, Crohn's Disease, Ulcerative Colitis

Status
Active
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
TECCU Software
Sponsored by
Grupo Espanol de Trabajo en Enfermedad de Crohn y Colitis Ulcerosa
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Inflammatory Bowel Disease

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

No Intervention

Active Comparator

Arm Label

control group

TECCU group

Arm Description

Outcomes

Primary Outcome Measures

clinical remission
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

cost-effectiveness
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.

Full Information

First Posted
July 24, 2023
Last Updated
September 1, 2023
Sponsor
Grupo Espanol de Trabajo en Enfermedad de Crohn y Colitis Ulcerosa
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1. Study Identification

Unique Protocol Identification Number
NCT06031038
Brief Title
Impact of Telemonitoring in the Management of Complex IBD in Spain: M-TECCU
Acronym
M-TECCU
Official Title
Impact of Telemonitoring in the Management of Complex Inflammatory Bowel Disease in Spain: TECCU Multicenter Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 1, 2020 (Actual)
Primary Completion Date
April 30, 2023 (Actual)
Study Completion Date
April 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Grupo Espanol de Trabajo en Enfermedad de Crohn y Colitis Ulcerosa

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Bowel Disease, Crohn's Disease, Ulcerative Colitis, Telemedicine

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
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.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
290 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
control group
Arm Type
No Intervention
Arm Title
TECCU group
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
TECCU Software
Intervention Description
patient monitoring by software application
Primary Outcome Measure Information:
Title
clinical remission
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.
Time Frame
52 weeks
Secondary Outcome Measure Information:
Title
cost-effectiveness
Description
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.
Time Frame
52 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Castany Pla
Organizational Affiliation
Spanish Working Group on Crohn's disease and ulcerative colitis (GETECCU)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario y Politécnico la Fe
City
Valencia
ZIP/Postal Code
46026
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
30482739
Citation
Del Hoyo J, Nos P, Faubel R, Munoz D, Dominguez D, Bastida G, Valdivieso B, Correcher M, Aguas M. A Web-Based Telemanagement System for Improving Disease Activity and Quality of Life in Patients With Complex Inflammatory Bowel Disease: Pilot Randomized Controlled Trial. J Med Internet Res. 2018 Nov 27;20(11):e11602. doi: 10.2196/11602.
Results Reference
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PubMed Identifier
30578197
Citation
Aguas M, Del Hoyo J, Faubel R, Munoz D, Dominguez D, Bastida G, Navarro B, Barrios A, Valdivieso B, Correcher M, Nos P. A Web-Based Telemanagement System for Patients With Complex Inflammatory Bowel Disease: Protocol for a Randomized Controlled Clinical Trial. JMIR Res Protoc. 2018 Dec 21;7(12):e190. doi: 10.2196/resprot.9639.
Results Reference
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PubMed Identifier
33339564
Citation
Del Hoyo J, Aguas M. Cost-effectiveness of Telemedicine-directed Specialized vs Standard Care for Patients With Inflammatory Bowel Diseases in a Randomized Trial. Clin Gastroenterol Hepatol. 2021 Jan;19(1):206-207. doi: 10.1016/j.cgh.2020.06.016. No abstract available.
Results Reference
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Impact of Telemonitoring in the Management of Complex IBD in Spain: M-TECCU

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