Image

Lifestyles and Breast Cancer

Recruiting
18 years of age
Female
Phase N/A

Powered by AI

Overview

Background: In Spain, 1 out of every 11 women will have a breast cancer before the age of 85 years and breast cancer is the leading cause of potential years of life lost. The randomized intervention in PREDIMED trail, using Mediterranean diet with free provision of extra virgin olive oil (MedDiet+EVOO) dramatically and significantly reduced the occurrence of cases of postmenopausal breast cancer.

Objectives: Assess the efficacy of a nutritional intervention with MedDiet+EVOO for the prevention of relapses among women with early breast cancer.

Methods: Randomized, multicenter trial (LifeBreast) among 766 women diagnosed with early breast cancer. Participants will be randomized in a 1:1 ratio to i) MedDiet+EVOO or ii) low-fat diet. Changes in circulating tumor cells, inflammatory biomarkers, oxidative stress and quality of life will be evaluated. The intervention will be delivered by face-to-face interviews with study dietitian, phone calls, and online tools. Participants in the MedDiet+EVOO group will receive 0.5l/week of EVOO and participants in the low-fat group will receive allotments of different foods, both at no cost. Generalized estimating equations will be used to estimate between-group differences in the following outcomes: circulating tumor cells, inflammatory biomarkers, oxidative stress, and quality of life will be evaluated.

Eligibility

Inclusion Criteria:

        Women with primary pathologically confirmed invasive breast adenocarcinoma in stages I, II
        or IIIA
        Exclusion Criteria:
          -  breast cancer recurrence
          -  in situ CDIS or LDIS
          -  inability or unwillingness to give written informed consent
          -  difficulty to comply with the intervention
          -  lack of willpower to change their diet (using the models of Prochaska and DiClemente)
          -  inability or unwillingness to communicate with study personnel
          -  medical condition that prevents the intervention (digestive disease with fat
             intolerance; severe psychiatric, neurological or endocrine disease; or allergy or
             hypersensitivity to any of the key foods of the intervention (EVOO or nuts) or
             impossibility to follow a Mediterranean diet and/or EVOO intake
          -  immunodeficiency or HIV-positive status
          -  concomitant condition that limits life-expectancy to less than 1 year
          -  difficulty or impossibility for an adequate follow-up
          -  institutionalized patients with lack of autonomy
          -  impossibility for attending group sessions and yearly follow-up visits or for
             telephone contact
          -  usual alcohol consumption >80 g/d
          -  BMI>40
          -  Patients with acute infection or inflammatory process (e.g. pneumonia) may be included
             in the study three months after the resolution of the infectious symptoms

Study details

Malignant Tumor of Breast

NCT04174391

University of Navarra

26 January 2024

Step 1 Get in touch with the nearest study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.