Fruit and Vegetable Intervention in Lactating Women to Reduce Breast Cancer Risk

NCT ID: NCT04374747

Last Updated: 2022-11-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

400 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-10-24

Study Completion Date

2024-04-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Mechanistic data show that compounds in fruits and vegetables have anti-inflammatory and anti-carcinogenic properties that can reduce breast cancer risk. However, observational and interventional studies have provided mixed results, and a recent report by the American Institute for Cancer Research (AICR) concludes that the data are insufficient but suggestive that non-starchy vegetables and foods containing carotenoids reduce risk. Measurement error, relatively low levels of carotenoid-rich fruit and vegetable intake in the study populations, emphasis on diet in later adulthood, and confounding factors likely contribute to the weak associations. Therefore, the investigators will conduct a randomized diet intervention trial in young women to assess the extent to which at least 8 to 10 daily servings of deeply pigmented and nutrient dense fruits and vegetables reduces biomarkers of breast cancer risk. The intervention is focused on breastfeeding women because: 1) pregnancy and lactation are normal early life course events; 2) the risk of pregnancy-associated breast cancer (PABC) is increased for up to 10 years postpartum; 3) a dietary intervention to reverse the detrimental molecular changes associated with puberty and pregnancy is more likely to be successful in younger than in older women;4) a diet rich in fruits and vegetables is hypothesized to reduce the inflammation during lactation/weaning and lower PABC risk; 5) postpartum lactating women may be a highly motivated population; and 6) breastmilk provides access to the breast microenvironment and breast epithelial cells to non-invasively assess the diet intervention directly in the breast. Four hundred nursing mothers will be randomly assigned to either the intervention arm, in which they are asked to increase fruit and vegetable intake to at least 8 to 10 daily servings for one year, or to a control condition in which participants receive a dietary guideline for breastfeeding mothers. Women in the intervention arm will receive counseling and boxes of fruits and vegetables for the first 20 weeks, after which they will continue to receive counseling. Changes in DNA methylation and cytokine profiles in breastmilk will be evaluated. Maternal weight and body fat distribution, and infant growth will be monitored. These results will greatly expand our knowledge of how diet alters molecular pathways in a specific organ, ultimately contributing to both breast cancer etiology and prevention.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Overview of home visits and activities completed by all participants

Visit 1 Introductory Visit (1.5 hours) 24-Hour Dietary Recalls completed during the week (1-2 hours) Occurs at 5 weeks postpartum

* Informed Consent document administered.
* Public Data Sharing Informed Consent document administered.
* Three questionnaires: New Moms Health, Physical Activity, and Breastfeeding Practices
* Maternal height, weight, and waist circumference measured.
* Instructions provided for future collection of biospecimens.
* Complete one 24-Hour Dietary Recall
* Instructions provided for two additional 24-Hour Dietary Recalls.

Visit 2 Sample Collection 1 (1.5 hours) Occurs at 6 weeks postpartum

* Provide bilateral breast milk samples and completed questionnaire.
* Provide infant stool sample and completed questionnaire.
* Two questionnaires: Infant Feeding, and Medication \& Supplement
* Infant length and weight measured.
* Maternal and infant skin carotenoids measured.
* Nutrition education provided.
* Optional collection of maternal stool sample and completed questionnaire.

Visit 3 Sample Collection 2 (1.5 hours) 24-Hour Dietary Recalls completed during the week (1-2 hours) Occurs at 16 weeks postpartum

* Provide bilateral breast milk samples and completed questionnaire.
* Provide infant stool sample and completed questionnaire.
* Three questionnaires: Physical Activity, Infant Feeding, and Medication \& Supplement
* Infant length and weight measured.
* Maternal weight and waist circumference measured.
* Maternal and infant skin carotenoids measured.

Visit 4 Sample Collection 3 (1.5 hours) 24-Hour Dietary Recalls completed during the week (1-2 hours) Occurs at 26 weeks postpartum

* Provide bilateral breast milk samples and completed questionnaire.
* Provide infant stool sample and completed questionnaire.
* Three questionnaires: Physical Activity, Infant Feeding, and Medication \& Supplement.
* Infant length and weight measured.
* Maternal weight and waist circumference measured.
* Maternal and infant skin carotenoids measured.
* Optional collection of maternal stool samples and completed questionnaire.

Visit 5 Sample Collection 4 (1.5 hours) 24-Hour Dietary Recalls completed during the week (1-2 hours) Occurs at 58 weeks postpartum

* Provide bilateral breast milk samples and completed questionnaire.
* Provide infant stool sample and completed questionnaire.
* Four questionnaires: Physical Activity, Infant Feeding, Medication and Supplement, and Breast Health
* Infant length and weight measured.
* Maternal weight and waist circumference measured.
* Maternal and infant skin carotenoids measured.
* Optional collection of maternal stool samples and completed questionnaire.

Annual Follow-up Visit (Maximum of 2) (1 hour) 24-Hour Dietary Recalls completed during the week (1-2 hours) Occurs at one-year intervals after Visit 5

* Three questionnaires: Physical Activity, Breast Health, Young Child Feeding
* Infant height and weight measured.
* Maternal weight and waist circumference measured.
* Maternal and infant skin carotenoids measured.

Monthly Inquiry (1 - 2 minutes) Occurs monthly until no longer breastfeeding

• Complete the Breast Feeding Update Questionnaire online via a survey sent through REDCap, or through a phone call.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Breast Cancer Female Inflammation Postpartum Weight Retention Diet, Healthy Risk Reduction

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors
Key laboratory analyses will conducted by laboratories blinded to intervention arm.

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Dietary Intervention

Intensive dietary counseling and fruit and vegetable box delivery.

Group Type EXPERIMENTAL

Dietary Counseling

Intervention Type BEHAVIORAL

The counseling approach will employ strategies shown to be successful in previous and ongoing dietary modification studies including supportive and motivational interviewing techniques. Each woman in the diet intervention group will be assigned a trained nutrition coach/counselor. Counselors will focus on helping participants identify and address barriers to achieving the goal of consuming at least 8 to 10 servings of nutrient dense fruits and vegetables each day (e.g., modifying recipes and food preparation). Participants will also receive weekly boxes of fruits and vegetables .

Information

Control condition of information on healthy eating during breastfeeding

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Dietary Counseling

The counseling approach will employ strategies shown to be successful in previous and ongoing dietary modification studies including supportive and motivational interviewing techniques. Each woman in the diet intervention group will be assigned a trained nutrition coach/counselor. Counselors will focus on helping participants identify and address barriers to achieving the goal of consuming at least 8 to 10 servings of nutrient dense fruits and vegetables each day (e.g., modifying recipes and food preparation). Participants will also receive weekly boxes of fruits and vegetables .

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Have given birth in past five weeks or are currently pregnant
* Breastfeeding baby at entry into the study
* Consuming five or fewer servings of fruits and vegetables daily at baseline
* Live within 25 miles of Amherst MA

Exclusion Criteria

* Invasive breast cancer
* Any cancer except non-melanoma skin cancer in past five years
* History of Crohn's disease, celiac sprue, or other malabsorption syndrome, which may interfere with digesting or absorption of nutrients
* A personal history of diabetes (excluding gestational diabetes)
* Baseline BMI of \<18.5
* Dietary restrictions that prevent participant from eating 8 to 10 servings of fruits and vegetables
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

National Cancer Institute (NCI)

NIH

Sponsor Role collaborator

University of Massachusetts, Amherst

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Kathleen Arcaro, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Massachusetts, Amherst

Lindiwe Sibeko, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Massachusetts, Amherst

Susan Sturgeon, DrPH

Role: PRINCIPAL_INVESTIGATOR

University of Massachusetts, Amherst

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University of Massachusetts Amherst

Amherst, Massachusetts, United States

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

United States

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Kathleen Arcaro, PhD

Role: CONTACT

413-577-1823

Susan Sturgeon, DrPH

Role: CONTACT

413-577-1364

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Kathleen Arcaro, PhD

Role: primary

References

Explore related publications, articles, or registry entries linked to this study.

Essa AR, Browne EP, Punska EC, Perkins K, Boudreau E, Wiggins H, Anderton DL, Sibeko L, Sturgeon SR, Arcaro KF. Dietary Intervention to Increase Fruit and Vegetable Consumption in Breastfeeding Women: A Pilot Randomized Trial Measuring Inflammatory Markers in Breast Milk. J Acad Nutr Diet. 2018 Dec;118(12):2287-2295. doi: 10.1016/j.jand.2018.06.015. Epub 2018 Sep 10.

Reference Type BACKGROUND
PMID: 30213617 (View on PubMed)

Sturgeon SR, Sibeko L, Balasubramanian R, Arcaro KF. New Moms Wellness Study: the randomized controlled trial study protocol for an intervention study to increase fruit and vegetable intake and lower breast cancer risk through weekly counseling and supplemental fruit and vegetable box delivery in breastfeeding women. BMC Womens Health. 2022 Sep 24;22(1):389. doi: 10.1186/s12905-022-01967-9.

Reference Type DERIVED
PMID: 36153518 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

1R01CA230478-01A1

Identifier Type: NIH

Identifier Source: secondary_id

View Link

2019-5382

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Dietary Sugars Found In Breast Milk
NCT02940795 COMPLETED NA