Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04584294 · ClinicalTrials.gov registry record · NA

Patient-Centered Reproductive Decision Support Tool for Women Veterans

A NA study of Contraception and Contraception Behavior, sponsored by VA Office of Research and Development.

Completed
Registry status
NA
Development phase
465
Enrollment target
12
Study locations

NCT04584294: Completed NA study of Contraception and Contraception Behavior, sponsored by VA Office of Research and Development.

NCT04584294 is a NA study of Contraception and Contraception Behavior that has completed, run by VA Office of Research and Development. The registered enrollment target is 465 participants, roughly in line with the 448-participant average among 72 other Contraception trials with a reported enrollment target. The trial reports 12 study locations across 9 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04584294, a NA study of Contraception and Contraception Behavior, has completed, sponsored by VA Office of Research and Development.

COMPLETED
Registry status
NA
Development phase
465 participants
Enrollment target
12
Study locations

Study Summary

The investigators have developed a web-based decision support tool to help women Veterans get the information and care they need to achieve their reproductive goals, whether that includes optimizing their health before desired pregnancies or birth control to avoid unwanted pregnancies. The study will test the effect of sending a weblink to the decision tool to women Veterans prior to primary care visits at the VA. Half of participants will be sent a weblink before their appointment, and half will not be sent the link. The investigators hypothesize that participants who are sent the link will be more likely to report patient-centered discussions of their reproductive needs at visits, feel confident in communicating with their health care providers, have accurate knowledge about reproductive health, and choose birth control methods that best fit their preferences and needs.

Primary Outcome

Self-report of whether a discussion occurred during the scheduled primary care visit about pregnancy goals, prepregnancy health, or contraception that included shared decision making (SDM). SDM is measured by participant self-report with the CollaboRATE scale, which uses three 5-point Likert scale questions to assess SDM (score 0-12, with higher scores indicating more shared decision making; SDM defined using a top box score).

Interventions

  • BEHAVIORAL MyPath Web-Based Informational and Decision Support Tool

Study Locations (12)

Texas

  • El Paso VA Health Care System, El Paso, TX - El Paso
  • Michael E. DeBakey VA Medical Center, Houston, TX - Houston
  • South Texas Health Care System, San Antonio, TX - San Antonio
  • Central Texas Veterans Health Care System, Temple, TX - Temple

California

  • VA San Diego Healthcare System, San Diego, CA - San Diego

Colorado

  • Rocky Mountain Regional VA Medical Center, Aurora, CO - Aurora

Florida

  • Orlando VA Medical Center, Orlando, FL - Orlando

Georgia

  • Atlanta VA Medical and Rehab Center, Decatur, GA - Decatur

North Carolina

  • Durham VA Medical Center, Durham, NC - Durham

Pennsylvania

  • VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA - Pittsburgh

Utah

  • VA Salt Lake City Health Care System, Salt Lake City, UT - Salt Lake City

Trial Details

FieldValue
Enrollment Target 465 participants
Start Date 2021-03-01
Est. Completion 2025-09-30
Phase NA
VA Office of Research and Development

1,668 total trials

What the finished NCT04584294 record still lists

NCT04584294 is an interventional study that assigns participants to a tested intervention. The registered 465 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 448-participant average among 72 other Contraception trials with a reported enrollment target.

The record links to 4 conditions, with Contraception appearing as the primary indexed condition, and to 1 intervention - of which MyPath Web-Based Informational and Decision Support Tool is the first listed.

NCT04584294 lists 12 locations in 9 states (Texas, California, Colorado).

Frequently Asked Questions

What is clinical trial NCT04584294 about?

NCT04584294 is a clinical study titled "Patient-Centered Reproductive Decision Support Tool for Women Veterans". The investigators have developed a web-based decision support tool to help women Veterans get the information and care they need to achieve their reproductive goals, whether that includes optimizing their health before desired pregnancies or birth control to avoid unwanted pregnancies. The study wil...

What is the current status of trial NCT04584294?

This trial is currently completed. It is a NA study. The enrollment target is 465 participants. The study started on 2021-03-01. Estimated completion is 2025-09-30.

What conditions does trial NCT04584294 study?

This clinical trial studies the following conditions: Contraception, Contraception Behavior, Reproductive Health, Prepregnancy Health.

What interventions are being tested in trial NCT04584294?

The interventions under investigation include: MyPath Web-Based Informational and Decision Support Tool (BEHAVIORAL).

Who is sponsoring clinical trial NCT04584294?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04584294 being conducted?

This trial has 12 study locations across California, Colorado, Florida, Georgia, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Contraception

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 NCT04584294's enrollment target sits among peer trials

465 23rd of 72 higher than 50 of 72 other Contraception trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Contraception 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

  • NCT06717698 · 465 participants · Phase 2

    A Research Study Comparing How Well Different Doses of the Medicine NNC0519-0130 Can Reduce Kidney Damage in People Living With Chronic Kidney Disease

  • NCT07420283 · 465 participants · Phase 2

    A Study of Brenipatide in Participants With Opioid Use Disorder

  • NCT05312879 · 466 participants · Phase 2

    Phase 2/3 Adaptive Study of VX-147 in Adult and Pediatric Participants With APOL1- Mediated Proteinuric Kidney Disease

  • NCT06917404 · 466 participants · Phase 3

    A Study to Investigate the Treatment Effect of Subcutaneous Injections of Pentosan Polysulfate Sodium Compared With Placebo in Adult Participants With Knee Osteoarthritis Pain.

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

Source: ClinicalTrials.gov NCT04584294, the US trial registry maintained by the National Library of Medicine. NCT04584294 (mid enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.