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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03483610
Other study ID # RSRB00070962
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 25, 2018
Est. completion date May 31, 2019

Study information

Verified date August 2019
Source University of Rochester
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 450
Est. completion date May 31, 2019
Est. primary completion date May 31, 2019
Accepts healthy volunteers No
Gender Female
Age group 21 Years to 65 Years
Eligibility Inclusion Criteria:

- Registered patient in the Emergency Department of the University of Rochester Medical Center

- Women

- 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Provider Referral
Participants will be asked if they are up-to-date on their cervical cancer screening. If not they will be referred to a provider. At the end of the study they will receive a 10 minute follow up telephone survey to collect data screening status and views on cervical cancer screening.
Text Messaging
Participants will be asked if they are up-to-date on their cervical cancer screening. If not they will be referred to a provider. They will also receive a total of 3 text messages at 30-day intervals encouraging follow-up for cervical cancer screening. They will receive a 10 minute follow up telephone survey to collect data screening status and views on cervical cancer screening.

Locations

Country Name City State
United States University of Rochester, Department of Emergency Medicine Rochester New York

Sponsors (2)

Lead Sponsor Collaborator
University of Rochester National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of participants who scheduled or completed cervical cancer screening 150 days
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