← Back to Clinical Trials
Recruiting NCT06703567

NCT06703567 IMproving PAtient UndeRstanding of GEP TEst Results: Phase 4

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06703567
Status Recruiting
Phase
Sponsor European Institute of Oncology
Condition Breast Cancer
Study Type INTERVENTIONAL
Enrollment 82 participants
Start Date 2024-09-06
Primary Completion 2025-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Standard PolicyStandard Policy + GEP Information Film

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 82 participants in total. It began in 2024-09-06 with a primary completion date of 2025-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The primary aim of the study is to determine if provision of a patient information film about Oncotype DX improves patients' knowledge and understanding about Gene Expression Profiling (GEP) test and risk of recurrence results in early breast cancer (EBC) patients, identified by their clinical teams as potentially benefiting from having their tumor samples sent for GEP analysis.

Eligibility Criteria

Inclusion Criteria: * First presentation of early stage breast cancer with all known disease surgically removed * Estrogen Receptor (ER) positive and Human Epidermal growth factor Receptor 2 (HER-2) negative * No clear decision on whether chemotherapy should be given as adjunct based on current prognostic criteria * Consented to GEP testing * Able to give full informed consent to IMPARTER study * Good comprehension of the Italian language * Access to internet connection and devices (e.g. smart phone, tablet, laptop or desktop computer) Exclusion Criteria: * Other breast cancer diagnosis (e.g. Ductal carcinoma in situ, Metastatic) * Unable to give fully informed consent * Under 18 years of age * Unable to understand and speak Italian * No access to internet connection or devices

Contact & Investigator

Central Contact

Gabriella Pravettoni, MD

✉ gabriella.pravettoni@ieo.it

📞 +39 0257489731

Principal Investigator

Gabriella Pravettoni, MD

PRINCIPAL INVESTIGATOR

European Istitute of Oncology

Frequently Asked Questions

Who can join the NCT06703567 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Breast Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06703567 currently recruiting?

Yes, NCT06703567 is actively recruiting participants. Contact the research team at gabriella.pravettoni@ieo.it for enrollment information.

Where is the NCT06703567 trial being conducted?

This trial is being conducted at Milan, Italy.

Who is sponsoring the NCT06703567 clinical trial?

NCT06703567 is sponsored by European Institute of Oncology. The principal investigator is Gabriella Pravettoni, MD at European Istitute of Oncology. The trial plans to enroll 82 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology