Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT04092530 · ClinicalTrials.gov registry record · NA
Linking Inter-professional Newborn and Contraception Care
A NA study, sponsored by Rush University Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 2,518
- Enrollment target
NCT04092530: Completed NA study, sponsored by Rush University Medical Center.
NCT04092530 is a NA study that has completed, run by Rush University Medical Center. The registered enrollment target is 2,518 participants, above the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (79% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04092530, a NA study, has completed, sponsored by Rush University Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 2,518 participants
- Enrollment target
Study Summary
Pregnancies conceived within 18 months of a prior delivery (termed short inter-pregnancy interval \[IPI\]) place mothers and infants at high risk for poor health outcomes and affect nearly one third of women in the U.S. Rates of postpartum (PP) contraception use remain low, particularly among low-income minority women, leading to high rates of short IPI pregnancies. This proposed study aims to address the gap in the current model of PP contraception care, by developing and implementing a novel approach to link (co-schedule) PP contraception care with newborn well-baby care with the goal of improving access to timely PP contraception.
Primary Outcome
Using de-identified patient data collected through clinic's Electronic Health Record (EHR) system (i.e., visit type attended, billing codes for contraception) we will measure receipt of all methods of contraception by two months postpartum
Interventions
- BEHAVIORAL LINCC intervention - enable co-schedule feature
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,518 participants |
| Start Date | 2021-04-01 |
| Est. Completion | 2024-06-30 |
| Phase | NA |
What the finished NCT04092530 record still lists
NCT04092530 is an interventional study that assigns participants to a tested intervention. Its 2,518 participants enrollment target places it among the larger protocols in the corpus, above the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (79% higher).
The record links to 0 conditions, and to 1 intervention - of which LINCC intervention - enable co-schedule feature is the first listed.
NCT04092530 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT04092530 about?
NCT04092530 is a clinical study titled "Linking Inter-professional Newborn and Contraception Care". Pregnancies conceived within 18 months of a prior delivery (termed short inter-pregnancy interval \[IPI\]) place mothers and infants at high risk for poor health outcomes and affect nearly one third of women in the U.S. Rates of postpartum (PP) contraception use remain low, particularly among low-in...
What is the current status of trial NCT04092530?
This trial is currently completed. It is a NA study. The enrollment target is 2,518 participants. The study started on 2021-04-01. Estimated completion is 2024-06-30.
What interventions are being tested in trial NCT04092530?
The interventions under investigation include: LINCC intervention - enable co-schedule feature (BEHAVIORAL).
Who is sponsoring clinical trial NCT04092530?
This trial is sponsored by Rush University Medical Center, which has 320 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT04092530's enrollment target sits among peer trials
2,518 44th of 2000 higher than 1,957 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT04142177 · 2,529 participants · NA
Sequential and Comparative Evaluation of Pain Treatment Effectiveness Response
- NCT00018057 · 2,530 participants · Phase 2
Study of Neuro-Cognitive Correlates of Pediatric Anxiety Disorders
- NCT00001160 · 2,500 participants
Studies on Tumors of the Thyroid
- NCT01904188 · 2,500 participants
Clinical Microbial Species & Antibiotic Resistance ID in ED Patients Presenting With Infection - is Rapid ID Possible & Accurate?
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI