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A Self-Guided Breastfeeding Program

NCT02989766 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 335

Last updated 2017-11-21

No results posted yet for this study

Summary

This intervention would be a series of self-help-style educational and motivational activity sheets for patients to complete independently. This will be a randomized clinical control trial.

Subjects will complete a pre delivery questionnaire and a postpartum questionnaire. Subjects in the intervention arm will complete 3 activity sheets prenatally during their wait time at the clinic. The first worksheet can be completed the day of recruitment after consent is signed.

Subjects will be contacted by phone at 3 and 6 months postpartum to assess long term duration of breast feeding.

Conditions

  • Breastfeeding

Interventions

BEHAVIORAL

Education on Breast Feeding

Subjects in the intervention arm will complete 3 activity sheets prenatally-study related.

Sponsors & Collaborators

  • St. Louis University

    lead OTHER

Principal Investigators

  • Jaye Shyken, MD · St. Louis University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
14 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-08-20
Primary Completion
2017-07-27
Completion
2017-07-27

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02989766 on ClinicalTrials.gov