search
Back to results

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

Primary Purpose

Breast Cancer Female, Inflammation, Postpartum Weight Retention

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Dietary Counseling
Sponsored by
University of Massachusetts, Amherst
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Breast Cancer Female

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

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

Sites / Locations

  • University of Massachusetts AmherstRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Dietary Intervention

Information

Arm Description

Intensive dietary counseling and fruit and vegetable box delivery.

Control condition of information on healthy eating during breastfeeding

Outcomes

Primary Outcome Measures

DNA methylation
% methylation in 300,000 CpG sites in DNA from sloughed breast epithelial cells from milk
Inflammatory markers in milk
Adiponectin, CRP, IFN-y, IL1-beta, Leptin, IL-6, IL-8, TNF-alpha, b-FGF, FLT-1, PLGF, VegF-D
Early weight
maternal weight
Early waist circumference
maternal waist circumference
One-year Weight
maternal weight
One-year Waist Circumference
maternal weight circumference

Secondary Outcome Measures

Full Information

First Posted
April 30, 2020
Last Updated
November 3, 2022
Sponsor
University of Massachusetts, Amherst
Collaborators
National Cancer Institute (NCI)
search

1. Study Identification

Unique Protocol Identification Number
NCT04374747
Brief Title
Fruit and Vegetable Intervention in Lactating Women to Reduce Breast Cancer Risk
Official Title
Fruit and Vegetable Intervention in Lactating Women to Reduce Breast Cancer Risk: Effects on Breast Cell DNA Methylation, Breast Inflammation,and Weight
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 24, 2019 (Actual)
Primary Completion Date
April 1, 2024 (Anticipated)
Study Completion Date
April 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Massachusetts, Amherst
Collaborators
National Cancer Institute (NCI)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer Female, Inflammation, Postpartum Weight Retention, Diet, Healthy, Risk Reduction

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Key laboratory analyses will conducted by laboratories blinded to intervention arm.
Allocation
Randomized
Enrollment
400 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Dietary Intervention
Arm Type
Experimental
Arm Description
Intensive dietary counseling and fruit and vegetable box delivery.
Arm Title
Information
Arm Type
No Intervention
Arm Description
Control condition of information on healthy eating during breastfeeding
Intervention Type
Behavioral
Intervention Name(s)
Dietary Counseling
Intervention Description
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 .
Primary Outcome Measure Information:
Title
DNA methylation
Description
% methylation in 300,000 CpG sites in DNA from sloughed breast epithelial cells from milk
Time Frame
20 weeks
Title
Inflammatory markers in milk
Description
Adiponectin, CRP, IFN-y, IL1-beta, Leptin, IL-6, IL-8, TNF-alpha, b-FGF, FLT-1, PLGF, VegF-D
Time Frame
20 weeks
Title
Early weight
Description
maternal weight
Time Frame
20 weeks
Title
Early waist circumference
Description
maternal waist circumference
Time Frame
20 weeks
Title
One-year Weight
Description
maternal weight
Time Frame
One-year
Title
One-year Waist Circumference
Description
maternal weight circumference
Time Frame
one year
Other Pre-specified Outcome Measures:
Title
Fruit and Vegetable Intake
Description
servings per day
Time Frame
one year

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kathleen Arcaro, PhD
Phone
413-577-1823
Email
karcaro@umass.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Susan Sturgeon, DrPH
Phone
413-577-1364
Email
ssturgeon@schoolph.umass.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kathleen Arcaro, PhD
Organizational Affiliation
University of Massachusetts, Amherst
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lindiwe Sibeko, PhD
Organizational Affiliation
University of Massachusetts, Amherst
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Susan Sturgeon, DrPH
Organizational Affiliation
University of Massachusetts, Amherst
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Massachusetts Amherst
City
Amherst
State/Province
Massachusetts
ZIP/Postal Code
01003
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kathleen Arcaro, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is no plan to make IPD available to other researchers.
Citations:
PubMed Identifier
30213617
Citation
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.
Results Reference
background
PubMed Identifier
36153518
Citation
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.
Results Reference
derived

Learn more about this trial

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

We'll reach out to this number within 24 hrs