Evidence map›Paper›PMID 42819737›Full record

ArticlePregnancy (Hoboken, N.J.)2026

Optimizing outpatient cervical ripening: A mixed-methods study identifying implementation drivers during a multisite, randomized trial.

Rebecca F Hamm, Anthony C Sciscione, Brett D Einerson, Matthew K Hoffman, Robert M Silver, Miriam J Alvarez, Alison G Cahill, Lisa D Levine

Abstract read
In one paragraph

Article in Pregnancy (Hoboken, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

8 authors.

Rebecca F HammDepartment of Obstetrics & Gynecology Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA.ORCID https://orcid.org/0000-0002-2587-2054
Anthony C SciscioneDepartment of Obstetrics & Gynecology Christiana Care Health System Newark Delaware USA.
Brett D EinersonDepartment of Obstetrics & Gynecology University of Utah Health Salt Lake City Utah USA.ORCID https://orcid.org/0000-0003-1928-4333
Matthew K HoffmanDepartment of Obstetrics & Gynecology Columbia University New York New York New York USA.ORCID https://orcid.org/0000-0002-2927-8693
Robert M SilverDepartment of Obstetrics & Gynecology University of Utah Health Salt Lake City Utah USA.ORCID https://orcid.org/0000-0002-5794-3152
Miriam J AlvarezDepartment of Obstetrics & Gynecology Dell Medical School University of Texas Austin Texas USA.
Alison G CahillDepartment of Obstetrics & Gynecology Dell Medical School University of Texas Austin Texas USA.
Lisa D LevineDepartment of Obstetrics & Gynecology Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA.

Funding

A multicenter pragmatic randomized trial evaluating effectiveness and safety of outpatient Foley catheter for cervical ripening in nulliparous women: a Type 1 hybrid effectiveness-implementation studyR01HD109229 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI ALISON G CAHILL, LISA Danielle LEVINE · 2022 to 2026
$3.4M
NICHD NIH HHS R01 HD109229
6 · The paper itself

Abstract

Introduction: Data have demonstrated decreased time in the hospital and improved patient satisfaction when using outpatient cervical ripening with a Foley catheter as compared to routine in-hospital induction. An ongoing multisite trial (the COMFORT trial) is evaluating the impact of outpatient ripening on cesarean delivery, maternal and neonatal morbidity rates. Here, we aimed to characterize provider and organizational level determinants of implementation related to outpatient cervical ripening with a Foley catheter during the COMFORT trial. Methods: This sequential mixed-methods study (quan- > QUAL; December 2022 to January 2025) was embedded into an ongoing five-site randomized clinical trial comparing outpatient versus inpatient cervical ripening. Prior to trial initiation, surveys (quan) were distributed to obstetric clinicians at all sites. The survey collected demographics, Foley placement experience, perceived acceptability, and feasibility of outpatient Foley via validated measures [Likert; total 4-20]. One year into the trial, clinician focus groups (QUAL) assessed barriers, facilitators, and sustainability of outpatient Foley, guided by the Consolidated Framework for Implementation Research 2.0 and coded in an integrated approach. Results: A total of 396 clinicians (64% physicians, 22% nurses, 10% certified nurse midwives [CNMs], 4% nurse practitioners [NPs]/physician assistants [PAs]) completed the pre-trial survey; 29.2% had previously used outpatient ripening. Acceptability (19/20 interquartile range [IQR] [16-20]) and feasibility (16/20 IQR [15-20]) were high overall but varied by site ( Conclusion: This work identified key determinants influencing the implementation of outpatient cervical ripening with a Foley catheter. Findings (1) allowed for real-time adaptations to intervention workflow and utilization of new implementation strategies during the course of the multisite trial, and (2) can be utilized to drive success for current and future sites implementing outpatient Foley cervical ripening clinically.

Indexed as

cervical ripeningFoley catheterimplementation sciencelabor inductionmixed‐methodsorganizational determinantsprovider attitudes

Identifiers

PMID42819737
PMCPMC13624844

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.