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NCT Number: NCT06703567

IMproving PAtient UndeRstanding of GEP TEst Results: Phase 4

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

European Institute of Oncology

Milan, 20141, Italy

Location status: Recruiting

Location contact

Gabriella Pravettoni, MD

CONTACT

[email protected]

+39 0257489731

About this study

Advances made in our understanding of the molecular biology of breast cancer have improved diagnostic testing and therapeutic options available to patients. Importantly results from genomic testing provide more accurate tailoring of treatments potentially enhancing the benefit to harm ratio by only offering adjuvant chemotherapy to those patients at highest risk of recurrence, and sparing those at lower risk the unwanted side effects of cytotoxic treatment. Conversations about risks and optimal treatments can be complex.

To aid understanding about GEP tests many clinical teams provide patients with information leaflets about GEP testing. Unfortunately these are often written by either academic or commercial sponsors and designed to meet certain ethical and regulatory guidelines rather than effectively educate the end-user.

There is some evidence that user-friendly patient information films might enhance patient knowledge and understanding and are more accessible to certain individuals, especially those with low literacy.

IMPARTER project has developed eight-minute film explaining why Oncotype DX GEP tests is used in EBC, what it is, and how the results help determine whether or not chemotherapy is recommended as a useful treatment option.

This study wish to examine the utility of the information film in the clinic setting with EBC patients identified by their clinical teams as potentially benefiting from having their tumor samples sent for GEP analysis.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Standard Policy

Behavioral

Patients will receive information about the GEP test by clinical teams

Standard Policy + GEP Information Film

Behavioral

Patients will receive information about the GEP test by clinical teams and, after consultation with physician, they will be sent a link to view the film regarding OncotypeDX

Primary outcomes

  1. GEP Knowledge Evaluation

    Time frame: 1 week

    Collection of Gene Expression Profiling (GEP) Knowledge Questionnaire (higher total score indicates better understanding)

Secondary outcomes

  1. Anxiety assessment

    Time frame: 1 week

    Collection of Spielberger State/Trait Anxiety Inventory (STAI) questionnaire (minimum value: 1, maximum value: 4 - higher scores signify greater anxiety)

  2. Decision making assessment

    Time frame: 1 week

    Collection of Decisional Conflict Scale questionnaire (minimum value: 1, maximum value: 5 - higher scores mean a greater agreement with the statement)

  3. Reaction to uncertain situations assessment

    Time frame: 1 week

    Collection of Intolerance of Uncertainty Scale Short-Form (IUS-12) questionnaire (minimum value: 1, maximum value: 5 - higher scores mean a greater agreement with the statement)

  4. Physician confidence/satisfaction assessment

    Time frame: 1 week

    Collection of Confidence/satisfaction with GEP test result discussions questionnaire (higher scores indicate better satisfaction)

Study contacts

Contact information is provided by the study sponsor or research team.

Gabriella Pravettoni, MD

CONTACT

[email protected]

+39 0257489731

Mara Negri

CONTACT

[email protected]

+39 0257489536

Sponsors and collaborators

Lead sponsor

European Institute of Oncology

Other

Registry information

Acronym: IMPARTER

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Nov 25, 2024
Registry last updated
Dec 10, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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