Breastfeeding Support and Weight Management for Black Women

Weight Loss Clinical Trial

— MamaBear  

Official title:

Breastfeeding Support and Weight Management for Black Women: A Dual Intervention

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03480048
• Other study ID #: RC105989
• Secondary ID: 1R21HD085138-01A
• Status: Completed
• Phase: N/A
• Start date: March 22, 2017
• Est. completion date: November 30, 2018

Study information

• Verified date: August 2019
• Source: Michigan State University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study, in African American mothers in Detroit, will test an intervention that combines home visiting by experienced peer counselors with a smart phone-based weight control program. The investigators are trying to help mothers breastfeed their babies longer, and also help them get back to the weight they were before they were pregnant. This trial will help the investigators to guide policies in the state of Michigan and has the potential to improve the health of both mothers and babies everywhere.

Description:

Excessive pregnancy-related weight retention is an important determinant of obesity and is more common among African American women. At the same time, breastfeeding, which has been recommended as a strategy to decrease weight retention is lowest among African American women. This racial disparity in breastfeeding may partly explain the disparity in obesity, but even if the two are not causally related, a dual intervention designed to increase breastfeeding duration and decrease postpartum weight retention makes practical sense because both are associated with the same critical postpartum time window.

For this study, the investigators will incorporate a postpartum weight management component into an effective breastfeeding support program. This dual intervention will use a combination of in-person, telephone, and interactive web/mobile-based health counseling to provide education and support for breastfeeding difficulties and postpartum weight management. The intervention will be delivered by peer counselors who will be trained to provide support using motivational interviewing techniques with consultation by experts. The investigators have designed the dual intervention to provide encouragement, information, and problem-solving assistance at the appropriate pre or postpartum stage for both breastfeeding support and maternal weight management. The mixed delivery mode has proven effective in other settings and is important to build a trusting relationship while allowing frequent and flexible methods for communicating during this vulnerable time in a new mom's life. The overall goal of this developmental/exploratory R21 proposal is to gather pilot data to effectively refine the intervention so that it can be tested in a larger, longer study using a factorial design in a future R01 phase. The investigators will recruit, in one large inner-city prenatal care clinic (Henry Ford Health System, Detroit, MI), pregnant African American women (32-36 weeks gestation) who are considering breastfeeding (n=80), randomize them to the intervention or to a usual care group, and follow all participants to 20 weeks postpartum. The specific aims are to: 1) test feasibility; 2) assess acceptability; and 3) estimate the effect size of the intervention at 20 weeks postpartum relative to the usual care group on (1) breastfeeding duration and (2) postpartum weight retention. This project is significant because the combined intervention is designed to work synergistically on two interrelated, highly prevalent problems that disproportionately disadvantage African American families.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 53
• Est. completion date: November 30, 2018
• Est. primary completion date: November 30, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Pregnant, African American women, aged 18 and older, intending to breastfeed, ability to complete surveys in English

Exclusion Criteria:

• Contraindications to breastfeeding, high-risk pregnancy,

Related Conditions & MeSH terms

• Body Weight
• Breastfeeding
• Weight Loss

Intervention

Behavioral:
• Breastfeeding and weight loss support
The intervention is based on the Loving Support peer counseling breastfeeding model developed by the Special Supplemental Program for Women Infants and Children (WIC) with added components to promote postpartum weight loss.

Locations

Country	Name	City	State
United States	Henry Ford Health System, New Center One Women's Clinic	Detroit	Michigan

Sponsors (3)

Lead Sponsor	Collaborator
Michigan State University	Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Henry Ford Health System

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants Still Breastfeeding at 20 Weeks Postpartum	Count of women who report any breastfeeding at 20 weeks postpartum	20 weeks postpartum
Primary	Change in Weight From Baseline	Weight at 20 weeks postpartum minus pre-pregnancy weight.	Baseline and 20 weeks postpartum