Actively Recruiting
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
Led by Institut Claudius Regaud · Updated on 2026-04-20
200
Participants Needed
1
Research Sites
363 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
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
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older at study entry
- Diagnosed with hormone-dependent localized breast cancer requiring adjuvant hormonal therapy with tamoxifen
- Treated with tamoxifen for a maximum duration of 1 to 3 years
- Affiliated with a Social Security system in France
- Provided informed consent before participating in the study
You will not qualify if you...
- Pregnant or breastfeeding women
- Any psychological, family, geographical, or sociological condition preventing medical follow-up or study procedure compliance
- Patients under legal protection or who have forfeited their freedom by administrative or legal decision
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Institut Universitaire du Cancer de Toulouse - Oncopole
Toulouse, France, 31059
Actively Recruiting
Research Team
F
Florence DALENC
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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