Actively Recruiting

Age: 18Years +
All Genders
ID05548621

A Prospective Study to Evaluate the Implementation of Shared Decision Making Strategy for Renal Cell Cancer (RCC)

Led by St. Antonius Hospital · Updated on 2025-05-15

180

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

Sponsors

S

St. Antonius Hospital

Lead Sponsor

M

Merck Sharp & Dohme LLC

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the impact of two decision aids designed for patients with renal cell carcinoma (RCC) on how decisions about treatment are made and the quality of those decisions. This study focuses on both local (non-metastatic) and metastatic RCC, where treatment options vary widely depending on disease stage, tumor type, and patient preferences. The goal is to see how these decision aids affect shared decision-making between patients and healthcare professionals. The study compares usual care, where patients receive standard information, to care involving the use of two online interactive decision aids—one for local RCC and one for metastatic RCC. These aids explain treatment choices, outcomes, possible side effects, and benefits to help patients make informed decisions together with their doctors. The study is prospective and multicenter, involving groups before and after implementing the decision aids. Participants will be patients diagnosed with RCC who face treatment decisions covered by the aids. Assessments include observing shared decision-making during consultations and measuring decision quality, patient knowledge, and feelings about the decision process through questionnaires at intervals up to nine weeks after consultation. The study aims to evaluate changes in decision-making quality and how well the aids are implemented, with all data collected during and after consultations.

CONDITIONS

Brief Title

A Prospective Study to Evaluate the Implementation of Shared Decision Making Strategy for Renal Cell Cancer (RCC)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients clinically diagnosed with RCC
  • Patients facing a decision which is addressed in the decision aids (T1 tumor or metastatic disease)
  • Written informed consent
Not Eligible

You will not qualify if you...

  • Patients who are not able to fill in a questionnaire or undergo an interview individually

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 9 weeks after consultation

Participants with renal cell cancer are observed as they undergo usual care or use decision aids to support treatment decision-making.

1 consultation and follow-up assessments at 2 and 9 weeks after consultation

Trial Site Locations

Total: 1 location

1

St. Antonius Ziekenhuis

Nieuwegein, Utrecht, Netherlands, 3435 CM

Actively Recruiting

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Research Team

C

Cato Bresser

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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