CClinicalTrials.gg
Status unknownNCT02997384RIVIERAUpdated Dec 20, 2016

Feasibility of Breast Cancer Risk Evaluation in Women From the General Population

An observational study in Breastcancer, sponsored by Gustave Roussy, Cancer Campus, Grand Paris. Status unknown at 1 site in France. Open to female participants aged 40 Years to 74 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-12-20.

Sponsored by Gustave Roussy, Cancer Campus, Grand Paris · Observational

The sponsor has not verified this record recently (last verified Dec 2016), so the status shown — last known as Active, not recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
600
Ages
40 Years to 74 Years
Sex
Female
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Study summary

This study aims to evaluate the feasibility (acceptability) of a consultation dedicated to informing women about their risk of breast cancer and the screening methods recommended for them according to the recommendations in force during a routine consultation at a general practitioner, a gynecologist or a radiologist.

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Conditions studied

  • Breastcancer

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03

In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

This study's planned enrollment of 600 is above the median of 184 across 2,642 observational studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Gustave Roussy, Cancer Campus, Grand Paris is the lead sponsor of 242 studies on the registry; 65 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
40 Years to 74 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Women 40 to 74 years seen in consultation by their attending physician, gynecologist or radiologist

Inclusion criteria

  • Woman from 40 to 74 years old
  • Understanding the French language

Exclusion criteria

Exclusion Criteria:

Women will not be eligible for study if they are in any of the following situations:

  • Cancer active or in the course of treatment type surgery, chemotherapy, or radiotherapy, whether breast or other organ
  • Recent diagnosis \<1 year of suspicious or cancerous lesions
  • Psychiatric pathology not compatible with the study
  • Poor understanding of the French language
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
600 participants (estimated)
Patient registry
No

Groups and cohorts

  • General practitioner

    Other: Information

  • gynecologist

    Other: Information

  • radiologist

    Other: Information

Interventions

  • OtherInformation

    information of women about their risk of breast cancer and the screening methods recommended for them

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What researchers measure

Primary outcomes

  1. Percentage of women who agreed to measure their risk with personalized surveillance and screening recommendations during the consultation

    Time frame: up to 1 year

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Study locations

1 site
  • Gustave Roussy
    Villejuif, Val de Marne 94805, France
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 20, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02997384
Lead sponsor
Gustave Roussy, Cancer Campus, Grand Paris
Responsible party
Sponsor
First posted
Dec 20, 2016
Start date
Dec 2016
Primary completion
Jun 2017 (estimated)
Completion
Jun 2018 (estimated)
Last update
Dec 20, 2016

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2016. You cannot join it, but the record below documents what was studied.

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