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Clinical Trials/NL-OMON22492
NL-OMON22492
Recruiting
Not Applicable

Implementation and evaluation of shared decision-making, supported by outcome measures, regarding the organisation of follow-up care in breast cancer

Santeon0 sites630 target enrollmentTBD
ConditionsBreast cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast cancer
Sponsor
Santeon
Enrollment
630
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

.A.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Santeon

Eligibility Criteria

Inclusion Criteria

  • 1\) Patients must be facing the decision for the organisation of follow\-up care after receiving curative treatment for invasive breast cancer (in the first follow\-up consultation about 1 year after surgery); 2\) Being treated in a Santeon hospital; 3\) \= 18 years of age; 4\) Understand the Dutch language in speech and writing, and; 5\) Able to provide informed consent.

Exclusion Criteria

  • 1\) Patients diagnosed with non\-invasive breast cancer (e.g. Ductal Carcinoma In Situ (DCIS)); 2\) Patients who receive palliative treatment; 3\) Patients who received neoadjuvant therapy; 4\) Male breast cancer patients; 5\) Patients with dementia; 6\) Patients who received treatment for a recurrence or second primary tumor; 7\) Patients with a breast cancer\-related gene alteration (e.g. BRCA).

Outcomes

Primary Outcomes

Not specified

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