Informational Intervention in Increasing Lactation Practices by African American Women

Sponsor
Roswell Park Cancer Institute (Other)
Overall Status
Completed
CT.gov ID
NCT03680235
Collaborator
National Cancer Institute (NCI) (NIH)
296
1
2
35.6
8.3

Study Details

Study Description

Brief Summary

This trial studies how well an informational intervention works in increasing lactation practices by African American women. Giving additional information about breastfeeding and breast cancer risks to African American women may help doctors understand the factors that affect the decision to breast feed and to test whether providing useful information about breastfeeding will change breastfeeding behavior.

Condition or Disease Intervention/Treatment Phase
  • Other: Informational Intervention
  • Other: Informational Intervention
  • Other: Interview
  • Other: Survey Administration
N/A

Detailed Description

PRIMARY OBJECTIVES:
  1. Develop appropriate intervention strategies about the "breastfeeding-breast cancer connection" appropriate for use by experienced Women, Infants and Children (WIC) Peer Counselors (PCs) to disseminate to African-American mothers through a community-based participatory research (CBPR) approach including social media..

  2. Assess the comparative cognitive (e.g., knowledge, utility, cost-benefit), affective association (e.g., feelings), socioeconomic, familial and intent/outcome (e.g., breastfeeding) measures pre- and post-intervention to determine effectiveness of the content to impact cognitive and feeling measures and increase breastfeeding in young African-American mothers compared to an existing counseling program.

OUTLINE: Participants are assigned to 1 of 2 groups.

GROUP I: Participants receive standard information about pregnancy and breastfeeding. Participants may also participate in a focus group with their partner/spouse or family members after the baby's birth.

GROUP II: Participants receive standard information about pregnancy and breastfeeding as well as information about breastfeeding and breast cancer. Participants may also participate in a focus group with their partner/spouse or family members after the baby's birth.

After completion of the information intervention, participants are followed for up to 1 year.

Study Design

Study Type:
Interventional
Actual Enrollment :
296 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Novel Intervention to Increase Lactation Practices by African American Women
Actual Study Start Date :
Jul 11, 2016
Actual Primary Completion Date :
Jun 30, 2019
Actual Study Completion Date :
Jun 30, 2019

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Group I: (standard information about pregnancy, breastfeeding)

Participants receive standard information about pregnancy and breastfeeding. Participants may also participate in a focus group with their partner/spouse or family members after the baby's birth.

Other: Informational Intervention
Receive standard information about breastfeeding and pregnancy

Other: Interview
Participate in focus groups

Other: Survey Administration
Ancillary studies

Experimental: Group II (information about breastfeeding and cancer)

Participants receive standard information about pregnancy and breastfeeding as well as information about breastfeeding and breast cancer. Participants may also participate in a focus group with their partner/spouse or family members after the baby's birth.

Other: Informational Intervention
Receive standard information about breastfeeding and pregnancy

Other: Informational Intervention
Receive information about breastfeeding and cancer

Other: Interview
Participate in focus groups

Other: Survey Administration
Ancillary studies

Outcome Measures

Primary Outcome Measures

  1. Breastfeeding rates [Up to 1 year]

    Will be assessed by estimating a logistic regression model with breastfeeding as the dichotomous outcome variable and intervention condition as a predictor variable.

  2. Behavioral intentions for breastfeeding [Up to 1 year]

    Linear regression analyses will be conducted with condition and necessary covariates as predictors.

  3. Perceived risk for breast cancer [Up to 1 year]

    Linear regression analyses will be conducted with condition and necessary covariates as predictors. Will examine the degree to which perceived risk for breast cancer mediate any intervention impact on breastfeeding behavior and behavioral intentions.

  4. Affective associations with breastfeeding [Up to 1 year]

    Linear regression analyses will be conducted with condition and necessary covariates as predictors. Will examine the degree to which affective associations with breastfeeding mediate any intervention impact on breastfeeding behavior and behavioral intentions.

  5. Perceptions of benefits and barriers to breastfeeding [Up to 1 year]

    Linear regression analyses will be conducted with condition and necessary covariates as predictors. Will examine the degree to which perceptions of benefits and barriers to breastfeeding mediate any intervention impact on breastfeeding behavior and behavioral intentions.

  6. Qualitative analysis of focus group and key informant interviews [Up to 1 year]

    Will be recorded and transcribed. This text will be coded and categorized by Erwin following methods established in earlier research. The PEN-3 Model analysis will focus on the most salient factors as they apply to what will be considered the ?Positive, Existential, Negative? influences within the Cultural Empowerment domain in reference to breastfeeding and formula feeding topics. Will sort the responses into categories in a 3 x 3 table according to the Relationships and Expectations domain factors, ?Perceptions, Enablers, Nurturers,? on one axis, and the ?Positive, Existential, Negative? factors across the other axis. This categorical analysis will be reviewed and edited and the Women, Infants and Children (WIC) peer counselors (PCs) to increase validity of the process.

Eligibility Criteria

Criteria

Ages Eligible for Study:
14 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Pregnant African American women participating in the Catholic Charities WIC Program

  • INCLUSION - FOCUS GROUPS: Representative mothers, spouses/partners, influential family members (e.g., grandmothers, sisters) from the families served during the study.

  • INCLUSION - FOCUS GROUPS: Partners/spouses may include men or women.

Exclusion Criteria:
  • Unwilling or unable to follow protocol requirements.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Roswell Park Cancer Institute Buffalo New York United States 14263

Sponsors and Collaborators

  • Roswell Park Cancer Institute
  • National Cancer Institute (NCI)

Investigators

  • Principal Investigator: Deborah Erwin, Roswell Park Cancer Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Roswell Park Cancer Institute
ClinicalTrials.gov Identifier:
NCT03680235
Other Study ID Numbers:
  • I 270615
  • NCI-2018-00854
  • I 270615
  • R21CA202263
First Posted:
Sep 21, 2018
Last Update Posted:
Jul 23, 2020
Last Verified:
Jul 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No

Study Results

No Results Posted as of Jul 23, 2020