Nutrition Awareness Among Women With Non-Metastatic Breast Cancer
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Educational Brochure.
- Who it may be relevant to
- Registry conditions: Breast Cancer, Breast Cancer Metastatic. Basic parameters: from 18 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
This study explores perspectives of women with non-metastatic breast cancer regarding their willingness and ability to make dietary changes pertaining to foods/food products that may pose a risk to their cancer prognosis and survival. This is a single-group study conducted entirely online. All study activities, including consent, educational brochure and surveys, will be completed remotely. Participants will receive email invitations to complete questionnaires in REDCap. Questionnaire 1 will collect sociodemographic information (no PHI) and a brief dietary recall. Questionnaire 2 will assess identification of ultra-processed foods. Before Questionnaire 3, participants will review a two-page educational flyer explaining the link between diet, obesity, and cancer, with information on unhealthy calories and food processing. Questionnaire 3 will assess participants' willingness and ability to eat healthier foods and reduce unhealthy foods. At study completion, participants will receive a thank-you message and a brief satisfaction survey.
Interventions
- Behavioral Educational Brochure
The two-page educational brochure is emailed to participants after Questionnaire 2 and before they begin Questionnaire 3.
Primary outcome measures
- Willingness and ability to make dietary changes [Time frame: Baseline]
Eligibility criteria
Inclusion criteria
- Age >18 -Female
- Diagnosis of non-metastatic breast cancer
- Completion of primary treatment for breast cancer
- No recurrence or metastasis; or no other cancer other than basal or squamous cell
- Willingness to provide a private email address for all study activities
- Ability to read and understand English
Exclusion criteria
- Inability to comply with one or more of the inclusion criteria
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Health services research
Study locations
United States · 1 center
- UNC Cancer Hospital — Chapel Hill
Identifiers
NCT: NCT07389967 · 25-2834