Breast Cancer Clinical Trials

Find Breast Cancer Clinical Trials Near You

Evaluation of a Virtual Risk-reduction Intervention Among Women at Higher Than Average Risk of Breast Cancer in the European MyPeBS Screening Trial

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Breast cancer remains the most common cancer among women and a major cause of death despite advances in screening and treatment. Current screening programs are not personalized and are experiencing declining participation. A promising strategy for breast cancer control would be to implement risk-based prevention and early screening, targeting individuals at high risk of developing breast cancer, in order to improve chances of cure and reduce the need for more intensive treatments. The MyPeBS study was designed to assess whether personalized breast cancer screening (based on an individual's risk of developing breast cancer) is as effective as, or more effective than, current standard screening. Lifestyle interventions involving changes in diet or physical activity, for example, have been shown to be effective in reducing the risk of developing breast cancer, whether low or high. The MyPeBS study evaluates personalized screening but offers limited information on breast cancer prevention. MyPREV is a project that aims to assess the feasibility and impact of a personalized online program on breast cancer risk reduction measures. This program is offered to women at high risk of developing breast cancer as part of the European MyPeBS screening study. The main objective is to evaluate adherence to a personalized, online breast cancer prevention program focused on lifestyle and its acceptance among women at high or very high risk of developing cancer who participated in the MyPeBS study.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 40
Maximum Age: 74
Healthy Volunteers: t
View:

• Female (whether born female or not)

• Women aged 40 to 74 years (inclusive)

• Women who have participated in, or are participating in the MyPeBS study and who fulfilled all the inclusion and non-inclusion criteria for the MyPeBS study.

• Women able to express their non-opposition to participate in the intervention

• Women who were assessed as being at high (≥≥1.67% - 5.9%) or very high (≥≥6%) risk of invasive breast cancer at 5 years in the MyPeBS study

Locations
Other Locations
France
Centre Médical et Dentaire de Lyon MGEN
RECRUITING
Lyon
Gustave Roussy
NOT_YET_RECRUITING
Villejuif
Italy
AOU Città della Salute e della Scienza - CPO PiedmontSSD Epidemiologia e Screening
NOT_YET_RECRUITING
Torino
Time Frame
Start Date: 2026-02-19
Estimated Completion Date: 2027-06
Participants
Target number of participants: 1508
Treatments
Other: intervention
intervention
Related Therapeutic Areas
Sponsors
Collaborators: European Union
Leads: UNICANCER

This content was sourced from clinicaltrials.gov