Clinical Trials Directory

Trials / Completed

CompletedNCT02427399

Conducting Outreach to Improve Cervical Cancer Screening Rates Among Underscreened Patients

Conducting Outreach to Improve Cervical Cancer Screening Rates Among Underscreened Patients at an Urban Community Health Center

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
1,100 (actual)
Sponsor
Fenway Community Health · Academic / Other
Sex
Female
Age
21 Years – 64 Years
Healthy volunteers
Accepted

Summary

The purpose of this project is to determine whether outreach to HIV-negative patients who are overdue for a Pap smear at a New England urban community health center can increase cervical cancer screening rates. It additionally seeks to determine which form of outreach - via letter, email, phone, or a mixture of those modalities- is most effective among these patients.

Detailed description

To the investigators' knowledge, this study will be the first to assess the efficacy of email in cervical cancer screening outreach in a randomized controlled trial. It will also be one of the few randomized controlled trials to directly compare different outreach media directly, as opposed to different variations within a single medium (e.g. two different types of letters). Lastly, given the unique patient demographic makeup at Fenway, including a significant number of lesbian, bisexual and transgender patients, secondary subanalyses have the potential to significantly add to the investigators' knowledge of what media work best in conducting cervical cancer screening outreach with sexual and gender minorities, who are disproportionately underscreened compared to heterosexual cis-gendered women.

Conditions

Interventions

TypeNameDescription
OTHERLetter and informational sheetThe patients in this group will be mailed a letter at time 0. The letter will inform the patient that she is overdue for a Pap and will also contain an informational sheet about cervical cancer and Pap tests.
OTHEREmailThe same text shared in the letter will be sent as an email to the patients in this intervention group, again at time 0, 1, and 2 months, as necessary for nonresponders.
OTHERPhoneThe patient will be telephoned and informed that they are due for a Pap, and given the opportunity to schedule an appointment over the phone immediately. Patients will be contacted at time 0, 1, and 2 months as necessary for nonresponders.
OTHERMultimodalThe patient will be sent a letter/informational sheet at time 0. If she does not respond within one month, she will be sent an email. If she does not respond by 2 months after the start of the intervention period, she will be called.

Timeline

Start date
2013-01-01
Primary completion
2014-12-01
Completion
2017-01-01
First posted
2015-04-28
Last updated
2017-06-22
Results posted
2017-06-22

Source: ClinicalTrials.gov record NCT02427399. Inclusion in this directory is not an endorsement.