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Decision Aid - Extreme Prematurity

NCT01713894 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2018-01-12

No results posted yet for this study

Summary

The purpose of this study is to assess in a pilot randomized controlled trial the following PICOT question: In parents facing extreme premature delivery, does the use of an existing validated visual decision aid as compared to standard counseling, reduce the primary outcome of parental decisional conflict? Furthermore, is such a decision aid understood and applicable across differing populations of different ethnic backgrounds and social classes?

Conditions

  • Prematurity; Decision Support

Interventions

OTHER

Decision Aid

OTHER

Standard

Sponsors & Collaborators

  • Virtua Health

    collaborator OTHER

  • University of Michigan

    collaborator OTHER

  • Endeavor Health

    collaborator OTHER

  • Christiana Care Health Services

    lead OTHER

Principal Investigators

  • Ursula Guillen, MD · Christiana Care Health Systems

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2017-10-15
Completion
2017-10-15

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01713894 on ClinicalTrials.gov