Clinical trial Recruiting at 1 site Interventional Ages 18 to 90 Women only

Online program to support breast cancer patients with lifestyle changes

Official title: DianaWeb: Before and After Study Online Based Participatory Research to Test Whether Lifestyle and Diet Are Able to Reduce the Incidence of Recurrences (Local, Remote) or Secondary Cancers, Improve Prognosis and Survival of Breast Cancer

Run by Fondazione IRCCS Istituto Nazionale dei Tumori, Milano · NCT05057598 · Data updated 2026-11-12

This study is testing an online program to help breast cancer survivors in Italy make healthy lifestyle changes to see if it can improve their chances of staying well and feeling better.

Quick facts

Study typeInterventional
Ages18 Years to 90 Years
SexWomen only
Enrollment50000 (estimated)
SponsorFondazione IRCCS Istituto Nazionale dei Tumori, Milano
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Milan, MI)
StatusRecruiting
StartedJune 21, 2016
Main results expectedDecember 31, 2023
Study endsDecember 31, 2028
Registry record updatedSeptember 27, 2021
Trial IDNCT05057598 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are women diagnosed with breast cancer, including those with relapses or metastases, regardless of how long ago their initial diagnosis was.

Probably not a fit

Patients with a clinical diagnosis of Alzheimer's Disease or dementia, or those unable to use a personal computer or smartphone, may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

DianaWeb is a community-based participatory research initiative aimed at Italian women diagnosed with breast cancer. The program evaluates the effectiveness of lifestyle and nutrition interventions to improve patient prognosis through an interactive website that monitors lifestyle choices and collects clinical data. Participants receive evidence-based information and practical advice to encourage healthy lifestyle changes based on established cancer prevention guidelines. The study aims to recruit 50,000 breast cancer survivors to assess the impact of these interventions on recurrence and quality of life.

Why it matters

Potential benefit: If successful, this program could significantly improve the prognosis and quality of life for breast cancer patients through sustainable lifestyle changes.

How similar studies have gone: Other studies have shown success with similar lifestyle intervention approaches for cancer patients, indicating potential for positive outcomes.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Women with breast cancer diagnosis
* Women with breast cancer relapses
* Women with breast cancer metastases
* Women with breast cancer diagnosis even if many years have elapsed since the first diagnosis
* Women with breast cancer diagnosis and other tumors diagnosis
* Women with breast cancer diagnosis and other pathologists that impair cognitive abilities

Exclusion Criteria:

* Women with breast cancer diagnosis and clinical diagnosis of Alzheimer's Disease
* Women with breast cancer diagnosis and clinical diagnosis of dementia
* Women with breast cancer diagnosis unable to use personal computer and smart phone

Where it's running

  • Fondazione Irccs Istituto Nazionale Dei Tumori
    Milan, Mi, Italy
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.