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Clinical Trials/NCT03483610
NCT03483610CompletedNot Applicable

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

University of Rochester1 site in 1 country95 target enrollmentStarted: June 25, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
95
Locations
1
Primary Endpoint
Number of Participants Who Scheduled or Completed Cervical Cancer Screening

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
21 Years to 65 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

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

Arms & Interventions

screening and referral

Active Comparator

Intervention: Provider Referral (Behavioral)

behavioral intervention

Active Comparator

Intervention: Text Messaging (Behavioral)

Outcomes

Primary Outcomes

Number of Participants Who Scheduled or Completed Cervical Cancer Screening

Time Frame: 150 days

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

David Adler

Associate Professor of Emergency Medicine

University of Rochester

Study Sites (1)

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