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Clinical Trials in the Netherlands / NCT07046884
Recruiting Not applicable

Improving Personalized Treatment in Oncology: Effects of Integrated Oncological Decision-making

NCT07046884 · tracked via the Priya Life Science Netherlands tracker
Phase
Not applicable
Started
2024-03-25
Last updated
2025-07-02

Condition(s) studied

Oncology

Investigational drug(s) / intervention(s)

Integrated Oncological Decision-making Model

Integrated Oncological Decision-making Model: In the IODM-based practice, the following three information components should be incorporated when forming a personalized treatment plan: 1. State-of-the-art oncological treatment options with advantages and disadvantages; 2. General health status based on physical, psychosocial, and emotional functioning; 3. Goals and preferences of the patient, both in treatment and daily life. Together with the professionals, optimal tools and strategies to integrate these components within the care path will be discussed.

Study summary

The research aims to evaluate an Integrated Oncological Decision-making Model (IODM) to tailor oncological treatment plans to individual patients. The primary objective is to assess the impact of the IODM on personalized decision-making and patient outcomes. The study will employ a stepped-wedge cluster randomized trial design involving eight oncological care paths across four medical centers in the Netherlands. The study population consists of 400 adult patients (50 per care path) who will undergo treatment based on either standard clinical guidelines (control) or the IODM (intervention). The intervention involves integrating three key components: oncological treatment options, patient's general health status, and patient's goals and preferences. The main study parameters include measuring the discordance between recommendations based on medical information and final treatment decisions, assessing whether discordance reflects more personalized decision-making, and evaluating the implementation process of the IODM.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient's age = 18+ * Patient is included in participating oncological care path * Patient does not yet have a treatment plan * Patient, partner, or caregiver who reads and speaks Dutch sufficiently to understand the research material and to complete the questionnaires * Patient must be able to participate in the decision-making process Exclusion Criteria: • Patient, partner, or caregiver cannot give informed consent

Primary outcome measure(s)

Trial sites (4)

FacilityCityRegionStatus
University Medical Center Groningen (UMCG) Groningen Netherlands Recruiting
Leiden University Medical Center (LUMC) Leiden Netherlands Recruiting
Maastricht University Medical Center Maastricht Netherlands Recruiting
Zuyderland MC Sittard Netherlands Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07046884 on ClinicalTrials.gov ↗ ← All trials in the Netherlands