RECRUITING

Healthy for Two-Home Visiting (H42-HV): Health Coaching for Pregnant Women

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

The purpose of this study is to compare the effectiveness of H42-HV integrated into home visiting compared with usual home visiting services in reducing postpartum weight retention (difference between pre-pregnancy weight and weight at 6 months postpartum) among pregnant and postpartum participants. The overall goal is to improve long-term cardiometabolic health.

Official Title

Effectiveness of Health Coaching to Reduce Cardiometabolic Risk in Early Home Visiting Services

Quick Facts

Study Start:2023-04-25
Study Completion:2026-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05619705

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. * Pregnant, ≤33 weeks gestation
  2. * Singleton pregnancy
  3. * Pre pregnancy BMI≥25.0 Kg/m\^2 (calculated based on self-reported pre pregnancy height and weight)
  4. * Able to provide informed consent
  5. * English or Spanish speaking
  6. * Completion of screening and baseline data collection
  7. * Willing to participate in the intervention and data collection procedure (e.g., home weights)
  1. * Type 1 diabetes or taking insulin prior to delivery
  2. * Pregnant with multiple fetuses
  3. * Unable to walk 1 block without pain or shortness of breath
  4. * Not cleared by the study's clinicians or home visiting program staff
  5. * Planning to relocate from area during next 1 year
  6. * Active substance abuse disorder (except marijuana)
  7. * Psychiatric or substance use related hospitalization in past 1 year
  8. * Active eating disorder

Contacts and Locations

Study Contact

Kelly M Bower, PhD, MSN/MPH
CONTACT
410-955-4280
kbower1@jhu.edu
Wendy Bennett, MD,MPH
CONTACT
410-502-6081
wendy.bennett@jhmi.edu

Principal Investigator

Kelly Bower, PhD, MSN/MPH
PRINCIPAL_INVESTIGATOR
Johns Hopkins School of Nursing
Wendy Bennett, MD,MPH
PRINCIPAL_INVESTIGATOR
Johns Hopkins School of Medicine

Study Locations (Sites)

Johns Hopkins School of Nursing
Baltimore, Maryland, 21205
United States

Collaborators and Investigators

Sponsor: Johns Hopkins University

  • Kelly Bower, PhD, MSN/MPH, PRINCIPAL_INVESTIGATOR, Johns Hopkins School of Nursing
  • Wendy Bennett, MD,MPH, PRINCIPAL_INVESTIGATOR, Johns Hopkins School of Medicine

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 Date2023-04-25
Study Completion Date2026-06-30

Study Record Updates

Study Start Date2023-04-25
Study Completion Date2026-06-30

Terms related to this study

Keywords Provided by Researchers

  • Behavioral Intervention
  • Early Childhood Home Visiting
  • Overweight
  • Obesity
  • Postpartum
  • Pregnancy

Additional Relevant MeSH Terms

  • Postpartum Weight Retention
  • Pregnancy Weight Gain
  • Overweight and Obesity
  • Behavior, Health