RECRUITING

Better Birth Outcomes Through Technology, Education, and Reporting

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This is a pragmatic randomized control trial to evaluate the BETTER intervention compared to standard obstetrical care (control) to determine whether it helps to reduce maternal anemia and other adverse pregnancy outcomes. The BETTER intervention includes one motivational interviewing session and bi-weekly text messages to encourage patients to connect with resources that address their social needs, including housing, food, and transportation. Quantitative data will be used to study participant outcomes, including surveys, and electronic health record data.

Official Title

Better Birth Outcomes and Experiences Through Technology, Education, and Reporting (BETTER)

Quick Facts

Study Start:2024-02-26
Study Completion:2028-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06261398

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Ann McAlearney, ScD, MS
CONTACT
614-293-3716
Ann.McAlearney@osumc.edu
Nicole Thomas, PhD
CONTACT
614-247-6228
Nicole.Thomas3@osumc.edu

Principal Investigator

William Grobman, MD, MBA
PRINCIPAL_INVESTIGATOR
Ohio State University
Ann McAlearney, ScD, MS
PRINCIPAL_INVESTIGATOR
Ohio State University

Study Locations (Sites)

The Ohio State University Outpatient Care East
Columbus, Ohio, 43203
United States
McCampbell Hall
Columbus, Ohio, 43210
United States
The Ohio State University Wexner Medical Center OB/GYN Maternal and Fetal Medicine
Columbus, Ohio, 43210
United States

Collaborators and Investigators

Sponsor: Ohio State University

  • William Grobman, MD, MBA, PRINCIPAL_INVESTIGATOR, Ohio State University
  • Ann McAlearney, ScD, MS, PRINCIPAL_INVESTIGATOR, Ohio State University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-26
Study Completion Date2028-03

Study Record Updates

Study Start Date2024-02-26
Study Completion Date2028-03

Terms related to this study

Keywords Provided by Researchers

  • Social Determinants of Health (SDoH)
  • Pregnancy
  • Patient portals
  • Patient engagement
  • Disparities

Additional Relevant MeSH Terms

  • Pregnancy
  • Maternal Anemia
  • Pre-Term Birth
  • Hypertensive Disorders