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"Vasectomy: Right for Me?" Decision Support Tool

NCT07451067 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 750

Last updated 2026-07-23

No results posted yet for this study

Summary

The goal of this trial is to learn if a web-based decision aid designed to provide evidence-based information about vasectomy and other birth control options helps improve users' decision-making about birth control. The main questions it aims to answer are:

* Do people who use the decision aid have better knowledge about vasectomy?
* Do people who use the decision aid have lower conflict with their decision?

Participants will:

* Use the decision aid (if they are assigned to the intervention arm).
* Answer survey questions about their knowledge, decision-making, interest in vasectomy, and healthcare navigation experiences.

Conditions

  • Vasectomy
  • Contraception
  • Contraception Behavior
  • Reproductive Behavior

Interventions

BEHAVIORAL

"Vasectomy: Right for Me?" decision aid

The vasectomy decision aid is a web-based decision aid designed to help men make informed and value-concordant decisions about vasectomy.

Sponsors & Collaborators

  • University of Pittsburgh

    lead OTHER

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    collaborator NIH

  • Resound Research for Reproductive Health

    collaborator UNKNOWN

Principal Investigators

  • Sonya Borrero, MD, MS · University of Pittsburgh

  • Kari White, PhD, MPH · Resound Research for Reproductive Health

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
55 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-06-20
Primary Completion
2027-08-31
Completion
2027-08-31

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 NCT07451067 on ClinicalTrials.gov