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Behavioural Intervention

Intervention arm - ChatGPT for Birth Control

N/A
Recruiting
Led By Premal Patel, MD
Research Sponsored by University of Manitoba
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion period, estimated to be 2 months
Awards & highlights

Study Summary

This trial aims to improve pre-vasectomy consultations by reducing time and increasing satisfaction.

Eligible Conditions
  • Birth Control
  • Vasectomy

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion period, estimated to be 2 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion period, estimated to be 2 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Length of Consultation
Number of questions asked
Satisfaction of patients assessed by Likert scale
Secondary outcome measures
Commonly asked questions
Incidence of inaccurate ChatGPT responses

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Intervention arm - ChatGPTExperimental Treatment1 Intervention
Patient's interested in participating in the intervention group will be provided a secure ChatGPT account. They will have the opportunity to converse with ChatGPT to ask any potential questions they may have regarding their upcoming vasectomy. Patient's will then be seen for the standard pre-vasectomy consultation.
Group II: Control arm - no ChatGPTActive Control1 Intervention
No intervention - standard of care

Find a Location

Who is running the clinical trial?

University of ManitobaLead Sponsor
597 Previous Clinical Trials
199,392 Total Patients Enrolled
Premal Patel, MDPrincipal InvestigatorAssistant Professor, Department of Surgery. Director, Undergraduate Urologic Medical Education
1 Previous Clinical Trials
150 Total Patients Enrolled
~23 spots leftby May 2025
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