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The Role of Diet and Lifestyle in Breast Cancer Survival

The Role of Diet, Complementary Treatment and Lifestyle in Breast Cancer Progression and Survival

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00701584
Acronym
DietCompLyf
Enrollment
3390
Registered
2008-06-19
Start date
2005-01-31
Completion date
2014-12-31
Last updated
2014-05-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

Phytoestrogens, Isoflavones, Lignans, Breast cancer survival, breast cancer recurrence

Brief summary

Diet has been found to influence hormone production and metabolism which in turn could affect the incidence of hormone related cancers. Consumption of soy-containing foods, known to be rich in phytoestrogens, is thought to be one of the chemoprotective factors against breast cancer in Asian populations. Phytoestrogens have a wide range of metabolic effects and may have a role in effecting breast cancer risk. Although there is mounting evidence of the positive influence of phytoestrogens on breast cancer risk, very little research has been carried out in humans as to the effects of phytoestrogens on breast cancer recurrence and survival. The DietCompLyf study aims to explore this effect by carrying out an observational study in 3,000 breast cancer women in the UK. The effects of diet, lifestyle practices and use of complementary treatments will also be investigated. Participants are recruited 9-15 months post-diagnosis and followed up for 5 years. Questionnaires as well as blood and urine samples are collected annually.

Detailed description

Women matching the eligibility criteria are consented at breast cancer follow-up hospital visits. Blood and urine samples are then collected and questionnaires are provided for the participants to take away and return within 4 weeks. The process of sample collection and questionnaire provision is repeated for visit at years 3 and 5. Year 2 and 4 study visit vary in that questionnaires including a 7 day food diary are sent to participants at home to be filled in 7 days before their scheduled follow-up appointment. At hospital, blood and urine samples are collected as usual.

Interventions

None listed

Sponsors

United Kingdom Clinical Research Collaboration
CollaboratorOTHER
University College London Hospitals
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Women with histologically confirmed invasive primary breast cancer grades I to III. * age up to and including 75 years old

Exclusion criteria

* Previous cancer with the exception of basal cell carcinoma * Concomitant primary cancer * Bilateral cancer of the breast * Psychological problems * Cognitive impairment * Poor understanding of English

Design outcomes

Primary

MeasureTime frame
To assess the association between phytoestrogens and relapse free survivalUp to 5 years post-diagnosis

Secondary

MeasureTime frame
To assess the association between phytoestrogens and event free survivalUp to 5 years post-diagnosis
To assess the association between phytoestrogens and recurrence free survivalUp to 5 years post-diagnosis

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026