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Clinical Trials/NCT03483610
NCT03483610
Completed
N/A

Piloting Interventions to Improve Adherence to Cervical Cancer Screening Recommendations Among Emergency Department Patients

University of Rochester1 site in 1 country95 target enrollmentJune 25, 2018
ConditionsCervical Cancer

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cervical Cancer
Sponsor
University of Rochester
Enrollment
95
Locations
1
Primary Endpoint
Number of Participants Who Scheduled or Completed Cervical Cancer Screening
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to learn methods to encourage women to get recommended cervical cancer screening. Cervical cancer screening is an important part of cervical cancer prevention. The study team will determine if the patient is currently up-to-date with cervical cancer screening recommendations. If the patient is not up-to-date, then they will be randomly assigned to one of two interventions. One intervention consists only of referral to a women's health care provider to obtain cervical cancer screening. The other intervention consists of receiving a total of 3 text messages at 30-day intervals encouraging follow-up for cervical cancer screening.

Registry
clinicaltrials.gov
Start Date
June 25, 2018
End Date
May 31, 2019
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

David Adler

Associate Professor of Emergency Medicine

University of Rochester

Eligibility Criteria

Inclusion Criteria

  • Registered patient in the Emergency Department of the University of Rochester Medical Center
  • Age 21 - 65

Exclusion Criteria

  • Past hysterectomy with cervical removal
  • Known infection with HIV (screening recommendations for women with HIV differ from the general population)
  • Non-English speaking
  • Inability to consent
  • Lack of text-capable mobile phone and/or inability to use text function

Outcomes

Primary Outcomes

Number of Participants Who Scheduled or Completed Cervical Cancer Screening

Time Frame: 150 days

Study Sites (1)

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