Bridging the Gap From Postpartum to Primary Care
NCT05543265 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 360
Last updated 2024-09-19
Summary
Chronic health conditions affect most older adults. Preventative medicine and risk management strategies, especially when applied earlier in life, are essential to altering the trajectory of a disease and ultimately improving health outcomes. Primary care providers (PCP) often provide most of these services, though younger adults are the least likely to receive primary care. This project leverages a period of high engagement and health activation during an individual's life (pregnancy) to nudge her toward use of primary care after the pregnancy episode. This randomized controlled trial will test the hypothesis that a behavioral science-informed intervention, incorporating defaults and salience, can increase the rates of PCP follow-up within 4 months following a delivery for individual with hypertension, diabetes, obesity. If successful, this intervention could serve as a scalable solution to increase primary care use and preventative health services in a population that currently has low rates of engagement and utilization of these services.
Conditions
- Hypertension
- Hypertension in Pregnancy
- Diabetes Mellitus
- Gestational Diabetes
- Obesity
- Depressive Disorder
- Anxiety Disorders
Interventions
- BEHAVIORAL
-
Default appointment scheduling
Default primary care appointment scheduling
- BEHAVIORAL
-
Targeted messaging
Patient-specific messages about the importance of postpartum care transition
- BEHAVIORAL
-
Nudge Reminders
Primary care appointment reminders
Sponsors & Collaborators
-
National Institute on Aging (NIA)
collaborator NIH -
National Bureau of Economic Research, Inc.
collaborator OTHER -
Massachusetts Institute of Technology
collaborator OTHER -
Massachusetts General Hospital
lead OTHER
Principal Investigators
-
Mark A Clapp, MD, MPH · Massachusetts General Hospital
-
Jessica L Cohen, PhD · Harvard School of Public Health (HSPH)
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-11-03
- Primary Completion
- 2023-10-11
- Completion
- 2024-07-23
Countries
- United States
Study Locations
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