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Clinical Trials/NCT04253977
NCT04253977
Recruiting
Phase 2

Promoting Healthy Weight Across the Pregnancy and Postpartum Period Through Dissemination of an Evidence Based Intervention

Washington University School of Medicine1 site in 1 country784 target enrollmentFebruary 3, 2020
ConditionsObesity

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Obesity
Sponsor
Washington University School of Medicine
Enrollment
784
Locations
1
Primary Endpoint
Change in weight
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

This project evaluates the effectiveness of an evidence-based intervention (HEALTH-P2) to prevent excessive weight gain from pregnancy through 12 months postpartum when disseminated and implemented in real-world settings, through Parents as Teachers. To enhance the impact of HEALTH-P2, the study also evaluates implementation outcomes from the training curriculum (implementation strategy) and external validity when HEALTH-P2 is implemented within this national home visiting organization. This partnership has potential for significant impact on obesity and chronic diseases such as cardiovascular disease and diabetes.

Detailed Description

Women are exceptionally vulnerable during childbearing years to gain disproportionally large amounts of weight when compared to men or other life periods. Weight gained during pregnancy and retained after the postpartum period contributes to obesity development and progression. Evidence based lifestyle interventions addressing the trajectory of weight gain across the childbearing continuum can reverse these alarming trends of excessive weight among young women, but have had limited uptake due to time, expense, and parenting priorities. To address this gap, our research team developed the lifestyle intervention Healthy Eating, Activity Living, Taught at Home during Pregnancy and Postpartum (HEALTH-P2) in partnership with Parents as Teachers (PAT). This study will provide evidence for the dissemination and implementation (D\&I) of HEALTH-P2 across PAT's network of sites, promoting healthy weight on a national scale. The study builds on our previous work with a pragmatic cluster randomized controlled trial to evaluate D\&I of HEALTH-P2 across multiple levels to achieve widespread impact. First, we will determine weight outcomes (12-month postpartum weight; gestational weigh gain) among 336 overweight/obese women (N=168 HEALTH-P2; N=168 usual care) when parent educators (\~8/site) from PAT sites nationwide receive the HEALTH-P2 training through PAT National Center's existing training infrastructure and conduct HEALTH-P2 as part of routine practice. From a D\&I perspective, an evaluation guided by RE-AIM will measure implementation outcomes (acceptability, appropriateness, feasibility, fidelity, adaptation). Further, the Conceptual Framework for Implementation Research will guide an assessment of contextual factors that influence external validity at multiple levels (mother, parent educator, PAT site).

Registry
clinicaltrials.gov
Start Date
February 3, 2020
End Date
March 31, 2025
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Deliver PAT at a site participating in the study
  • Provide informed consent

Exclusion Criteria

  • At least 18 years of age
  • For the participants:
  • Inclusion Criteria:
  • 18-45 years of age
  • overweight or obese (BMI over 25 kg/m2) before becoming pregnant
  • English or Spanish speaking
  • participating or willing to participate in PAT at a participating PAT site until baby turns 1
  • able to give informed consent for participation
  • Exclusion Criteria:
  • planning to become pregnant again before their baby turns 1

Outcomes

Primary Outcomes

Change in weight

Time Frame: 12 months postpartum

Mother's body weight

Secondary Outcomes

  • Fidelity of delivery to the intervention(throughout intervention delivery, which can range from 2-4 years for parent educators depending on when their site is randomized)

Study Sites (1)

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