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RecruitingNCT05989776EVAPREFUpdated Dec 12, 2024

Increasing Access to Fertility Preservation for Women with Breast Cancer

An interventional study of Informational brochure for patients and brief training for oncologists in Breast Cancer, sponsored by University Paul Sabatier of Toulouse. Recruiting at 2 sites in France. Open to female participants aged 18 Years to 40 Years. Per ClinicalTrials.gov, last updated 2024-12-12.

Sponsored by University Paul Sabatier of Toulouse · Not applicable, Interventional, and Other

From the registry’s dates

  • Primary completion was expected by Dec 2025, 11 months ago, but the record still lists the study as recruiting.
  • Registered 1 year after the study started (first participant enrolled Jun 2022, registered Jun 2023).
  • Started Jun 2022; still recruiting 4 years 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
750
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
Female
01

Study summary

The EVAPREF project aims to increase access to fertility preservation by developing an approach to improve and evaluate existing information and coordination tools developed by the Pays-de-la-Loire and Occitanie Regional Cancer networks. First, the investigators will use a qualitative, iterative, user-centered and participatory approach to improve the current tools and create training content for the physicians who will use these tools. Second, the investigators will conduct a randomized stepped wedge trial of women under 40 newly treated with chemotherapy for breast cancer. The investigators will evaluate the rate of fertility preservation consultation before and after implementation of the improved tools, over a 30-month period from mid-2023 to the end of 2025. Finally, in a third step, the investigators will study their approach (context-sensitive implementation analysis) and provide key elements for its transferability to other contexts and in particular to other Regional Cancer networks in France.

Read the detailed description

Background:

With the increase in the number of long-term survivors, interest is shifting from cancer survival to life and quality of life after cancer. These include consequences of long-term side effects of treatment, such as gonadotoxicity. Fertility preservation is becoming increasingly important in cancer management. International recommendations agree on the need to inform patients prior to treatments about the risk of fertility impairment and refer them to specialized centers to discuss fertility preservation. However, the literature reveals suboptimal access to fertility preservation on an international scale, and particularly in France, making information for patients and oncologists a potential lever for action. The overall goal is to improve access to fertility preservation and related consultations for women with breast cancer through the development and evaluation of a combined intervention targeting the diffusion of information for these patients and brief training for oncologists.

Methods:

First, the investigators will use a qualitative, iterative, user-centered and participatory approach to improve existing information tools and create training content for oncologists (Aim 1). Second, the investigators will conduct a randomized stepped-wedge trial evaluating rate of fertility preservation consultation over a 30-month period (Aim 2). The investigators will include 750 women aged 18 to 40 newly treated with chemotherapy for breast cancer at one of 6 participating centers. The primary outcome will be rate of fertility preservation consultation before and after using the combined intervention (informational brochure for patients and brief training for oncologists) and will be analyzed using linear regression models.Third, the investigators will analyze their approach (context-sensitive implementation analysis) and provide key elements for transferability to other contexts in France (Aim 3).

Discussion:

After transitioning to the combined intervention, the investigators will expect to observe an increase in access to fertility preservation consultation. Particular attention will be paid to the effect of this intervention on socially disadvantaged women, who are known to be at greater risk of inappropriate treatment. In addition, the user-centric design principles and participatory approaches used to optimize the acceptability, usability and feasibility of the combined intervention will likely enhance its impact, diffusion and sustainability.

02

Conditions studied

  • Breast Cancer

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Keywords

  • Breast cancer
  • Fertility preservation
  • Information
  • Practitioner training
  • Social inequalities in health
  • Participatory approach
  • Combined intervention
03

In context

Breast Neoplasms

14,825 studies on the registry are indexed under Breast Neoplasms; 3,319 are open to participants now.

This study's planned enrollment of 750 is above the median of 72 across 10,896 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

University Paul Sabatier of Toulouse is the lead sponsor of 13 studies on the registry; 4 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients over 18 and under 40 years of age treated for newly diagnosed breast cancer and receiving chemotherapy.
  • People who are able to read the study information poster and the fertility preservation information brochure in French, either alone or with help from a caregiver or relative or an interpreter.
  • People with intellectual disability will be included as long as they are able able to read the study information poster and the fertility preservation information brochure in French alone or with help from a caregiver or relative or an interpreter..

Exclusion criteria

Exclusion Criteria:

  • People whose mental health status precludes participation in the study, as determined by the clinical team.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
750 participants (estimated)

Study arms

  • No intervention
    Usual care

    Usual care information to fertility preservation counseling

  • Active comparator
    Intervention: informational brochure for patients and brief training for oncologists

    The intervention is based on information provided to different target populations, using a variety of media, including brochures and videos.

    Behavioral: Informational brochure for patients and brief training for oncologists

Interventions

  • BehavioralInformational brochure for patients and brief training for oncologists

    For this randomized, stepped wedge trial, the investigators planned a mixed intervention that targets both health professionals and patients. This intervention will be carried out in its entirety thanks to the working groups made up of health professionals and expert patients that took place before the randomized trial. The intervention for health professionals consists of awareness training. They will be trained (or made aware) at different times, defined by randomization. The intervention for patients consists of a pictorial information brochure and tabular patient decision aid given by trained health professionals.

06

What researchers measure

Primary outcomes

  1. Rate of recourse to fertility preservation consultation before and after using the combined intervention

    This information will be collected by each regional screening coordination center of the two participating regions from the medical records of patients

    Time frame: up to 18 mont post enrollment

07

Study locations

2 of 2 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 12, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05989776
Lead sponsor
University Paul Sabatier of Toulouse
Collaborators
National Cancer Institute, France, Institut Claudius Regaud, Réseau Onco-Occitanie, Réseau ONCOPL
Responsible party
Marie-Anne Durand (Researcher, University Paul Sabatier of Toulouse) — Principal investigator
First posted
Aug 14, 2023
Start date
Jun 1, 2022
Primary completion
Dec 2025 (estimated)
Completion
Dec 2026 (estimated)
Last update
Dec 12, 2024

Study contacts

Marie-Anne Durand, PhD
Contact
marie-anne.durand@univ-tlse3.fr
0033648038356
Sébastien Lamy, PhD
Contact
lamy.sebastien@iuct-oncopole.fr
0033684449479
Marie-Anne Durand, PhD
principal investigator · Université Toulouse III Paul Sabatier

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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