Mobile app for tracking pregnancy symptoms
Piloting of JUN to Enhance Self-Efficacy Pregnant Women
This study is testing a mobile app designed to help pregnant women track their symptoms and see if it works better for those under community supervision compared to those who aren't.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years to 50 Years |
| Sex | Female |
| Sponsor | The University of Texas Health Science Center at San Antonio Academic / other |
| Locations | 1 site (San Antonio, Texas) |
| Trial ID | NCT06636110 on ClinicalTrials.gov |
What this trial studies
This pilot study evaluates the safety and effectiveness of the JUN mobile health app, which utilizes artificial intelligence to monitor symptoms and provide timely feedback to pregnant women. The research will compare the experiences of pregnant women with and without criminal justice oversight over a three-month period. The study will take place across three diverse locations: Texas, Oregon, and Minnesota, focusing on self-efficacy in using the app. The goal is to understand how community supervision impacts the use of this digital health intervention during pregnancy.
Who should consider this trial
Good fit: Ideal candidates are pregnant women aged 18-50 in their first six months of pregnancy, either on community supervision or without criminal system involvement.
Not a fit: Patients who are not pregnant or are beyond the first six months of pregnancy will not benefit from this study.
Why it matters
Potential benefit: If successful, this app could enhance pregnancy care and decision-making for women, particularly those under criminal justice supervision.
How similar studies have performed: While the use of mobile health apps in pregnancy care is growing, this specific approach focusing on criminal justice oversight is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Pregnant female 18-50 years 2. Within first 6 months of pregnancy 3. Either on community supervision or without criminal system involvement 4. Located in Texas, Minnesota or Oregon Exclusion Criteria: 1. Individuals who do not identify as women 2. Later pregnancy, beyond the first 6 months
Where this trial is running
San Antonio, Texas
- University of Texas Health Science Center at San Antonio — San Antonio, Texas, United States (Recruiting)
Study contacts
- Principal investigator: Allison Crawford, PhD — The University of Texas Health Science Center at San Antonio
- Study coordinator: Allison Crawford, PhD
- Email: crawfordad@uthscsa.edu
- Phone: 210-739-9921
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.