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NCT05264779 · ClinicalTrials.gov registry record · NA

The Periviable GOALS Decision Support Tool

A NA study of Pregnancy Complications and Premature Birth, sponsored by Indiana University.

Recruiting
Registry status
NA
Development phase
216
Enrollment target
10
Study locations

NCT05264779: Recruiting NA study of Pregnancy Complications and Premature Birth, sponsored by Indiana University.

NCT05264779 is a NA study of Pregnancy Complications and Premature Birth that is actively recruiting participants, run by Indiana University. The registered enrollment target is 216 participants, below the 3,785-participant average among 39 other Pregnancy Complications trials with a reported enrollment target (94% lower). The trial reports 10 study locations across 9 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05264779, a NA study of Pregnancy Complications and Premature Birth, is actively recruiting participants, sponsored by Indiana University.

RECRUITING
Registry status
NA
Development phase
216 participants
Enrollment target
10
Study locations

Study Summary

The Periviable GOALS (Getting Optimal Alignment around Life Support) decision support tool (DST) is meant to facilitate informed shared decision-making regarding neonatal resuscitation for families facing the threat of a periviable delivery (deliveries occurring between 22 0/7 - 25 6/7 weeks gestational age). It is designed for parents to review independent of their clinician, and is intended to supplement, not replace, clinician counseling. The focus of the DST is the provision of patient-centered outcomes information and assistance with values clarification regarding neonatal outcomes. This is a multisite, randomized controlled trial to test the effect of the Periviable GOALS DST on shared decision making and decision satisfaction. The investigators hypothesize that participants who utilize the GOALS DST will have improved shared decision making and higher decision satisfaction.

Primary Outcome

9-item Shared Decision Making Questionnaire (SDM-Q-9) administered in-person or via phone/Zoom call. Scores range from 0 to 100, with a higher score correlating to higher shared decision making.

Conditions Studied

Pregnancy Complications Premature Birth Obstetric Labor, Premature Obstetric Labor Complications Pregnancy Preterm

Interventions

  • OTHER Periviable GOALS DST

Study Locations (10)

California

  • The University of California San Diego - San Diego
  • University of California San Francisco - San Francisco

Connecticut

  • Yale University - New Haven

Illinois

  • Northwestern University - Chicago

Indiana

  • Indiana University - Indianapolis

Kansas

  • The University of Kansas Medical Center - Kansas City

Massachusetts

  • University of Massachusetts - Worcester

Ohio

  • The Ohio State University - Columbus

Pennsylvania

  • University of Pennsylvania - Philadelphia

Trial Details

FieldValue
Enrollment Target 216 participants
Start Date 2022-06-06
Est. Completion 2027-02
Phase NA
Indiana University

890 total trials

What NCT05264779 shows while recruiting

NCT05264779 is an interventional study that assigns participants to a tested intervention. The registered 216 participants enrollment target is mid-sized for trials with a published cap, below the 3,785-participant average among 39 other Pregnancy Complications trials with a reported enrollment target (94% lower).

The record links to 5 conditions, with Pregnancy Complications appearing as the primary indexed condition, and to 1 intervention - of which Periviable GOALS DST is the first listed.

NCT05264779 lists 10 locations in 9 states (California, Connecticut, Illinois).

Frequently Asked Questions

What is clinical trial NCT05264779 about?

NCT05264779 is a clinical study titled "The Periviable GOALS Decision Support Tool". The Periviable GOALS (Getting Optimal Alignment around Life Support) decision support tool (DST) is meant to facilitate informed shared decision-making regarding neonatal resuscitation for families facing the threat of a periviable delivery (deliveries occurring between 22 0/7 - 25 6/7 weeks gestati...

What is the current status of trial NCT05264779?

This trial is currently recruiting. It is a NA study. The enrollment target is 216 participants. The study started on 2022-06-06. Estimated completion is 2027-02.

What conditions does trial NCT05264779 study?

This clinical trial studies the following conditions: Pregnancy Complications, Premature Birth, Obstetric Labor, Premature, Obstetric Labor Complications, Pregnancy Preterm.

What interventions are being tested in trial NCT05264779?

The interventions under investigation include: Periviable GOALS DST (OTHER).

Who is sponsoring clinical trial NCT05264779?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05264779 being conducted?

This trial has 10 study locations across California, Connecticut, Illinois, Indiana, Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Learn More About Clinical Trials

Similar trials for Pregnancy Complications

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05264779's enrollment target sits among peer trials

216 22nd of 39 higher than 18 of 39 other Pregnancy Complications trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Pregnancy Complications 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

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More recruiting context for NCT05264779

Source: ClinicalTrials.gov NCT05264779, the US trial registry maintained by the National Library of Medicine. NCT05264779 (mid enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.