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Can extra support improve life after breast cancer? new study investigates

NCT ID NCT05116449

Knowledge-focused Sponsor: Ramsay Générale de Santé Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This study follows 310 women who had surgery for breast cancer to see how access to supportive care (like counseling or nutrition advice) affects their quality of life. Participants fill out several questionnaires about their physical, emotional, and social well-being over time. The goal is to understand which types of support help most, so hospitals can better meet patients' needs.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could show which supportive care services most improve quality of life after breast cancer surgery, helping hospitals design better care programs.
What could go wrong
This is an observational study using questionnaires, not testing a new treatment. It cannot prove cause and effect, and results may not apply to all patients.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 310 people

The number the study aims to enrol. It can still change while the study runs.

Started

Feb 2021

Expected to finish

Jan 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Women patient with breast cancer

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Woman with histologically confirmed invasive breast cancer for whom surgery is scheduled * Age\> 18 years old * Performance status ECOG \<2 * Patient speaking and understanding French and able to complete questionnaires * Patient affiliated or beneficiary of a social security scheme * Patient having read the information note and not objecting to the use of the data collected Exclusion Criteria: * male * Patient with metastatic breast cancer * Patient with bilateral breast cancer * History of cancer of less than 5 years * Active infection or other serious underlying condition that may prevent the patient from receiving treatment * History or progressive psychiatric illness * Person deprived of liberty or under guardianship * Inability to undergo medical monitoring for geographical, social or psychological reasons Indication of emergency amputation * Protected patient: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision * Pregnant, breastfeeding or parturient woman * Patient hospitalized without consent

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Conditions

The condition(s) this trial relates to.

female breast carcinoma invasive breast carcinoma

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Breast cancer female

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Hôpital Privé de l'Estuaire

    RECRUITING

    Le Havre, 76620, France

  • Institut du sein Drôme Ardèche

    RECRUITING

    Guilherand-Granges, 07500, France

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