Telemonitoring with TECCU of active Inflammatory Bowel Disease is Not Inferior to Standard Care: Short-term Results of a Multicentre Randomized Controlled Trial of GETECCU.


Journal

Journal of medical Internet research
ISSN: 1438-8871
Titre abrégé: J Med Internet Res
Pays: Canada
ID NLM: 100959882

Informations de publication

Date de publication:
21 Aug 2024
Historique:
medline: 27 8 2024
pubmed: 27 8 2024
entrez: 27 8 2024
Statut: aheadofprint

Résumé

Telemonitoring is not consistently superior to standard care for inflammatory bowel disease (IBD), yet non-inferiority may be an acceptable outcome if remote care is more efficient. To compare the remission time and quality of life of patients with an active IBD controlled by standard care or through the TECCU App (Telemonitoring of Crohn´s Disease and Ulcerative Colitis). A 2-arm, randomized, multicentre trial with a non-inferiority design was performed at 24 Spanish hospitals on adult patients with IBD who initiated immunosuppressant or biological therapy. Patients were randomized into telemonitoring (G_TECCU) or standard care groups (G_Control). The follow-up schedule was based on telemonitoring contacts through the TECCU App in G_TECCU, and on in-person visits and telephone calls in G_Control, as in clinical practice. In both groups, treatment was adjusted according to the evolution of disease activity and medication adherence, which were measured through specific indices and biological markers at each check-up. The primary outcome was time in remission after 12-weeks, with quality of life, medication adherence, adverse events and patient satisfaction as secondary outcomes. Of 169 patients enrolled, 158 were randomized, and 150 were analyzed per protocol: telemonitoring (n=71); control (n=79). After 12-week, the time in clinical remission was not inferior after telemonitoring (4.20 ±3.73 weeks) to that in the controls (4.32 ±3.28 weeks), with a mean difference between arms of -0.12 weeks (95% CI -1.25-,1.01), non-inferiority p=0.017). The mean reduction of CRP values was -15.40 mg/L (SD=90.15, P =0.195) in G_TECCU and -13.16 mg/L (SD=54.61, P =0.053) in G_control, without significant differences between the two arms (P=.726). Similarly, the mean improvement of FC levels was 832.3 mg/L (SD=1825.0, P=.003) in G_TECCU and 1073.5 mg/L in G_Control (SD=3105.7, P=.03), but differences were not significant (P=.965). Quality of life improved in both groups, with a mean rise in the IBDQ-9 score of 13.44 points in G_TECCU (SD=19.1; P<.001) and 18.23 points [SD=22.9]; P=.001) in G_Control. Moreover, the proportion of patients who adhered to their medication rose significantly from 35.2% (25/71) to 67.6% (48/71) in G_TECCU (P=.001) and from 45.6% (36/79) to 73.4% (58/79) in G_Control (P=.001). Satisfaction remained stable around 90%, although non-inferiority was not demonstrated for secondary outcomes. Telemonitoring patients with active IBD is not inferior to standard care to achieve and maintain short-term remission. TECCU may be an alternative follow-up tool if the improved health outcomes and costs are confirmed in the long-term. The trial is registered at ClinicalTrials.gov with the identifier NCT06031038; https://classic.clinicaltrials.gov/ct2/show/NCT06031038. RR2-10.2196/resprot.9639.

Sections du résumé

BACKGROUND BACKGROUND
Telemonitoring is not consistently superior to standard care for inflammatory bowel disease (IBD), yet non-inferiority may be an acceptable outcome if remote care is more efficient.
OBJECTIVE OBJECTIVE
To compare the remission time and quality of life of patients with an active IBD controlled by standard care or through the TECCU App (Telemonitoring of Crohn´s Disease and Ulcerative Colitis).
METHODS METHODS
A 2-arm, randomized, multicentre trial with a non-inferiority design was performed at 24 Spanish hospitals on adult patients with IBD who initiated immunosuppressant or biological therapy. Patients were randomized into telemonitoring (G_TECCU) or standard care groups (G_Control). The follow-up schedule was based on telemonitoring contacts through the TECCU App in G_TECCU, and on in-person visits and telephone calls in G_Control, as in clinical practice. In both groups, treatment was adjusted according to the evolution of disease activity and medication adherence, which were measured through specific indices and biological markers at each check-up. The primary outcome was time in remission after 12-weeks, with quality of life, medication adherence, adverse events and patient satisfaction as secondary outcomes.
RESULTS RESULTS
Of 169 patients enrolled, 158 were randomized, and 150 were analyzed per protocol: telemonitoring (n=71); control (n=79). After 12-week, the time in clinical remission was not inferior after telemonitoring (4.20 ±3.73 weeks) to that in the controls (4.32 ±3.28 weeks), with a mean difference between arms of -0.12 weeks (95% CI -1.25-,1.01), non-inferiority p=0.017). The mean reduction of CRP values was -15.40 mg/L (SD=90.15, P =0.195) in G_TECCU and -13.16 mg/L (SD=54.61, P =0.053) in G_control, without significant differences between the two arms (P=.726). Similarly, the mean improvement of FC levels was 832.3 mg/L (SD=1825.0, P=.003) in G_TECCU and 1073.5 mg/L in G_Control (SD=3105.7, P=.03), but differences were not significant (P=.965). Quality of life improved in both groups, with a mean rise in the IBDQ-9 score of 13.44 points in G_TECCU (SD=19.1; P<.001) and 18.23 points [SD=22.9]; P=.001) in G_Control. Moreover, the proportion of patients who adhered to their medication rose significantly from 35.2% (25/71) to 67.6% (48/71) in G_TECCU (P=.001) and from 45.6% (36/79) to 73.4% (58/79) in G_Control (P=.001). Satisfaction remained stable around 90%, although non-inferiority was not demonstrated for secondary outcomes.
CONCLUSIONS CONCLUSIONS
Telemonitoring patients with active IBD is not inferior to standard care to achieve and maintain short-term remission. TECCU may be an alternative follow-up tool if the improved health outcomes and costs are confirmed in the long-term.
CLINICALTRIAL BACKGROUND
The trial is registered at ClinicalTrials.gov with the identifier NCT06031038; https://classic.clinicaltrials.gov/ct2/show/NCT06031038.
INTERNATIONAL REGISTERED REPORT UNASSIGNED
RR2-10.2196/resprot.9639.

Identifiants

pubmed: 39189160
doi: 10.2196/60966
doi:

Banques de données

ClinicalTrials.gov
['NCT06031038']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Mariam Aguas (M)

Gastroenterology Department, La Fe University and Polytechnic Hospital and Health Research Institute La Fe, Av Fernando Abril Martorell 106, Valencia, ES.

Javier Del Hoyo (J)

Gastroenterology Department, La Fe University and Polytechnic Hospital and Health Research Institute La Fe, Av Fernando Abril Martorell 106, Valencia, ES.

Raquel Vicente (R)

Miguel Servet University Hospital, Zaragoza, ES.

Manuel Barreiro-de Acosta (M)

University Clinical Hospital, Santiago, ES.

Luigi Melcarne (L)

Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Sabadell, ES.

Alejandro Hernandez-Camba (A)

Nuestra Señora de la Candelaria University Hospital, Tenerife, ES.

Lucía Madero (L)

Dr Balmis General University Hospital, ISABIAL, Alicante, ES.
CIBERehd, Instituto de Salud Carlos III, Madrid, ES.

María Teresa Arroyo (MT)

Lozano Blesa Clinic University Hospital, Zaragoza, ES.

Beatriz Sicilia (B)

Burgos University Hospital, Burgos, ES.

María Chaparro (M)

CIBERehd, Instituto de Salud Carlos III, Madrid, ES.
Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Universidad Autónoma de Madrid, Madrid, Madrid, ES.

María Dolores Martin-Arranz (MD)

La Paz University Hospital, Faculty of Medicine, Universidad Autónoma de Madrid, Madrid, ES.
IdiPAZ - Instituto de Investigación Sanitaria del Hospital Universitario La Paz, Madrid, ES.

Ramón Pajares (R)

Infanta Sofía University Hospital, Madrid, ES.

Francisco Mesonero (F)

Ramón y Cajal University Hospital, Madrid, ES.

Miriam Mañosa (M)

Germans Trias i Pujol University Hospital, Badalona, ES.
CIBERehd, Instituto de Salud Carlos III, Madrid, ES.

Pilar Martinez (P)

San Cecilio Clinic University Hospital, Parque Tecnológico de la Salud (PTS), Granada, ES.

Silvia Chacón (S)

Morales Meseguer General University Hospital, Murcia, ES.

Joan Tosca (J)

Clinic University Hospital, Valencia, ES.

Sandra Marín (S)

Reina Sofía University Hospital, Córdoba, ES.
Maimonides Institute for Biomedical Research in Córdoba (IMIBIC), Córdoba, ES.

Luciano Sanroman (L)

Hospital Alvaro Cunqueiro, Vigo, ES.

Marta Calvo (M)

Puerta de Hierro University Hospital, Madrid, ES.

David Monfort (D)

Consorci Sanitari Terrasa, Barcelona, ES.

Empar Saiz (E)

Xarxa Assistencial University Hospital, Manresa, ES.

Yamile Zabana (Y)

Mútua Terrassa University Hospital, Terrassa, ES.
CIBERehd, Instituto de Salud Carlos III, Madrid, ES.

Ivan Guerra (I)

Fuenlabrada University Hospital, Madrid, ES.

Pilar Varela (P)

Cabueñes Universitary Hospital, Gijón, ES.

Virginia Baydal (V)

Gastroenterology Department, La Fe University and Polytechnic Hospital and Health Research Institute La Fe, Av Fernando Abril Martorell 106, Valencia, ES.

Raquel Faubel (R)

Joint Research Unit in ICT Applied to Reengineering Socio-Sanitary Process, IIS La Fe-Universitat Politècnica de València, Valencia, ES.
PTinMOTION-Physiotherapy in Motion Multispeciality Research Group, Department of Physiotherapy, Universitat de València, Valencia, ES.

Pilar Corsino (P)

Miguel Servet University Hospital, Zaragoza, ES.

Sol Porto-Silva (S)

University Clinical Hospital, Santiago, ES.

Eduard Brunet (E)

Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Sabadell, ES.

Melodi González (M)

Nuestra Señora de la Candelaria University Hospital, Tenerife, ES.

Ana Gutiérrez (A)

Dr Balmis General University Hospital, ISABIAL, Alicante, ES.

Pilar Nos (P)

Gastroenterology Department, La Fe University and Polytechnic Hospital and Health Research Institute La Fe, Av Fernando Abril Martorell 106, Valencia, ES.

Classifications MeSH