Precision Nudging Drives Wellness Visit Attendance at Scale
- Conditions
- PreventionWell VisitWomen's HealthAnnual VisitHealth Behavior
- Interventions
- Other: Precision nudgingOther: Standard of care
- Registration Number
- NCT05509049
- Lead Sponsor
- Lirio
- Brief Summary
The purpose of the present randomized controlled trial is to explore the effectiveness of a 12-month well woman digital health intervention leveraging Precision Nudging - the application of behavioral science and reinforcement learning to create individualized, tailored health messaging at scale that matches the right message to the right person at the right time - in promoting behavior change. Specifically, it is hypothesized that scaling behavioral science through reinforcement learning will be more effective at motivating participants to engage with well woman messages and to schedule and to attend a well woman visit compared to a standard of care message.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 30068
- Patient of health care system.
- Visit with OBGYN office in the last 36 months.
- OBGYN office provider is a Women's Wellness group approved provider.
- Completed a women's wellness within the last 366 days.
- Upcoming women's wellness appointment.
- Had a childbirth episode (e.g., C-section vaginal delivery, or other event, including stillbirth) within the last 3 months or has a pregnancy due date in the future.
- Unsubscribed.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Treatment Precision nudging Behavioral science and reinforcement learning-driven hyper-personalized messages Control Standard of care Standard of care message
- Primary Outcome Measures
Name Time Method Proportion of participants who scheduled a well woman visit 12 months Proportion of participants who attended a well woman visit 12 months Proportion of participants who scheduled a well woman visit and did not attend (and did not Cancel and/or Reschedule) 12 months
- Secondary Outcome Measures
Name Time Method Proportion of participants who opened and/or clicked Call-to-Action, or otherwise engaged with the communication(s) 12 months
Trial Locations
- Locations (1)
Rochester Regional Health
🇺🇸New York, New York, United States