Geriatric and Oncological Evaluation With Technology for Holistic Healthcare Management for Older Multimorbid Patients.

NCT05423808 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2024-08-12

No results posted yet for this study

Summary

The GerOnTe TWOBE study aims to evaluate the effectiveness of the GerOnTe intervention, consisting of a renewed, patient-centred, care pathway coordinated by an APN and supported by a Health Professional Consortium and IC Technology, compared to the current standard of care in the eight different Belgian and Dutch hospitals.

Conditions

  • Geriatrics
  • Medical Oncology
  • Critical Pathways
  • Digital Technology

Interventions

OTHER

Health Professional Consortium

In the intervention group, the renewed, patient-centred care pathway will be coordinated by the Advanced Practice Nurse (APN) and will be supported by digital technology. The intervention aims to increase the involvement of the patient in the treatment decision process, to provide comprehensive care through the quarterly meeting of all professionals involved in the care of the patient during a Health Professional Consortium (HPC) and to support patient empowerment by supporting self-management by using digital tools.

DEVICE

Holis Dashboard - Holis Patient App

In the intervention group, the renewed, patient-centred care pathway will be coordinated by the Advanced Practice Nurse (APN) and will be supported by digital technology. The intervention aims to increase the involvement of the patient in the treatment decision process, to provide comprehensive care through the quarterly meeting of all professionals involved in the care of the patient during a Health Professional Consortium (HPC) and to support patient empowerment by supporting self-management by using digital tools.

Sponsors & Collaborators

  • University of Bordeaux

    collaborator OTHER
  • Diakonessenhuis, Utrecht

    collaborator OTHER
  • University of Milan

    collaborator OTHER
  • University College Dublin

    collaborator OTHER
  • Oslo University Hospital

    collaborator OTHER
  • International Society of Geriatric Oncology

    collaborator OTHER
  • Dublin City University

    collaborator OTHER
  • Universitair Ziekenhuis Brussel

    collaborator OTHER
  • General Hospital Groeninge

    collaborator OTHER
  • AZ Sint-Jan AV

    collaborator OTHER
  • Catharina Ziekenhuis Eindhoven

    collaborator OTHER
  • Reinier de Graaf Groep

    collaborator OTHER
  • KU Leuven

    collaborator OTHER
  • Universitaire Ziekenhuizen KU Leuven

    lead OTHER

Principal Investigators

  • Hans Wildiers, prof. dr. · Coordinator multidisciplinary breast centre (MBC)

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-30
Primary Completion
2024-08-08
Completion
2024-08-08

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05423808 on ClinicalTrials.gov