Study to Evaluate the Impact of the Use of Alternative and Complementary Therapies on Therapeutic Adherence in Patients Treated With taMoxifen for Early Stage Breast Cancer

ConditionBreast Cancer
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorInstitut Claudius Regaud

About this trial

This is a pilot, prospective, interventional, monocentric study designed to evaluate, in a real-life situation, adherence to tamoxifen treatment as a function of the taking of alternative and complementary therapies in patients with localized hormone-dependent breast cancer.

200 patients will be included in the study.

Each patient will be followed for one day.

Eligibility criteria

Qualifiers

Age ≥ 18 years at entry into the study.

Patient treated for hormone-dependent localized breast cancer requiring adjuvant Hormonal Therapy (HT) with tamoxifen.

Patients treated with tamoxifen for a maximum of 1 to 3 years.

Patient affiliated with a Social Security system in France.

Disqualifiers

Pregnant or breastfeeding women.

Any psychological, family, geographical or sociological condition that does not allow the medical follow-up and/or the procedures foreseen in the study protocol to be respected.

Patient who has forfeited his/her freedom by administrative or legal award or who is under legal protection (curatorship and guardianship, protection of justice).

Trial design

Treatments tested in this trial

  • Treatment requiring adjuvant Hormonal Therapy (HT) with tamoxifen.

Treatment groups

200 Participants
are divided into 1 treatment group

Sponsors and collaborators