- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03918668
Study for the Knowledge of Risk Factors Associated With Breast Cancer in Women (Mamanut)
Observational Study to Understand the Risk Factors Associated With Breast Cancer in Women With a Recent Diagnosis at the Community of Madrid
Breast cancer is the most frequent tumor in Western women. In Spain about 26,000 new breast cancers are diagnosed each year. This type of tumor is increasing worldwide with an increase in aggressive neoplasms in young women. There are some risk factors responsible for this global increase: lifestyle, diet and body weight especially in postmenopausal women.
Some cell mutations, especially in the BRCA1, BRCA2 and p53 genes, are associated with a very high risk of this type of cancer. Some authors have calculated the contribution of various modifiable risk factors to the global burden of breast cancer, and they concluded that 21% of all breast cancer deaths are attributable to alcohol consumption, overweight and obesity, and lack of physical activity. Nowadays, there aren't specific studies in the Community of Madrid designed to know the risk factors related to breast cancer.
For this reason, it is proposed to carry out an observational study that collects detailed information about dietary habits, genetic factors and life quality of a group of women with recent diagnosis in pre or post-surgical phase.
Study Overview
Status
Intervention / Treatment
Detailed Description
- Storage of biological sample at the Hospital.
- Patient's breast pathology characteristics.
- Study of concomitant pathologies.
- Dietary study: "Frequency of Food Consumption" questionnaire referring to the last year eating habits before having been breast cancer diagnosed.
- Physical activity study in the year prior to the diagnosis of breast cancer.
- Anthropometric study: weight, size, waist circumference and body composition (% Fat mass,% Lean mass,% Body water).
- Study of other risk factors of breast cancer: age, family history, reproductive history, medications consumed...
- Biochemical study: biochemical variables of the last blood analysis performed on the volunteer in the hospital center.
- Saliva collection to proceed with the genetic analysis.
- Collection of stool sample to carry out the microbiota study.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Madrid, Spain, 28046
- Institute for Health Research IdiPAZ
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Older women than 18 years old
Newly diagnosed patients with a breast tumor (Phase I, II or III). Being in one of the following cases:
- Patient who has not yet received any treatment and the committee has decided that as a first treatment will receive chemo or radiotherapy.
- Patient who has just undergone surgery and is waiting to start adjuvant treatment with chemo or radiotherapy.
- Sign the informed consent.
Exclusion Criteria:
- Patients with stage IV disease.
- Associated Eating Disorders.
- Patients with dementia, mental illness or decreased cognitive function.
- Pregnant or lactating women.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dietary habits of a group of women with pre and post-surgical breast cancer
Time Frame: Six months
|
Frequency of Consumption of food questionnaire referring. The frequency varies between one time per day and one time per month for every type of food during the last 6 months. to the last year of the volunteer's eating habits before being breast cancer diagnosed |
Six months
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PI-2842
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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