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Implementation of Uterine Fibroid Option Grid Patient Decision Aids Across Five Organizational Settings

NCT03985449 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 748

Last updated 2023-02-28

No results posted yet for this study

Summary

UPFRONT is a study that aims to use two implementation frameworks - the Consolidated Framework for Implementation Research and the Normalization Process Theory - to guide the implementation of a uterine fibroid patient decision aid, known as Option Grid, at five diverse gynecology settings across the United States. Option Grid provides evidence-based information on the various treatment options to help women across socioeconomic strata with symptomatic uterine fibroids make a preference-sensitive decision.

Conditions

  • Uterine Fibroid

Interventions

OTHER

Uterine Fibroid Option Grid encounter patient decision aid (text only)

The uterine fibroid Option Grid patient decision aid facilitates choice awareness and deliberation about treatment options when clinicians and patients discuss the management of uterine fibroids. The content is organized in a tabular format and is based on patients' frequently asked questions.

OTHER

Uterine Fibroid Option Grid encounter patient decision aid (text + Pictures)

The Picture Option Grid uses the same evidence as the text version while integrating images and simpler text, thus utilizing pictorial superiority to help patients better understand and remember information more easily compared to just using words.

OTHER

Uterine Fibroid Option Grid encounter patient decision aid (online)

Clinicians can click a link in the electronic health record that will lead them to the EBSCO Health website where they can click the treatment options relevant to the patient and generate a decision aid.

Sponsors & Collaborators

  • Brigham and Women's Hospital

    collaborator OTHER

  • Mayo Clinic

    collaborator OTHER

  • Montefiore Medical Center

    collaborator OTHER

  • Barnes-Jewish Hospital

    collaborator OTHER

  • Patient-Centered Outcomes Research Institute

    collaborator OTHER

  • Dartmouth-Hitchcock Medical Center

    lead OTHER

Principal Investigators

  • Glyn Elwyn, MD, PhD · Dartmouth College

Study Design

Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-08-01
Primary Completion
2022-12-15
Completion
2023-01-15

Countries

  • United States

Study Locations

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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 NCT03985449 on ClinicalTrials.gov