Mobile Web App for Cervical Cancer Screening

(wPap Trial)

SR
ST
Overseen BySasheen T Stone, BA
Age: 18+
Sex: Female
Trial Phase: Academic
Sponsor: University of South Dakota
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

The overarching goal of this study is to increase cervical cancer (CC) screening rates among Indigenous women in the U.S. Specifically, the study aims to develop and evaluate a culturally tailored, multilevel, multimedia mobile web app intervention (wPap) for women of the Yankton Sioux Tribe (YST) living on the YST Reservation in South Dakota.

The wPap intervention will be tested in a randomized clinical trial (RCT) involving 120 YST women aged 25-65. Participants will be randomly assigned to either: (a) the wPap intervention group (n = 60), receiving personalized, culturally tailored multilevel multimedia messages through a mobile web app along with health navigator support, or (b) a waitlist control group (n = 60), receiving printed educational materials on cervical cancer and screening guidelines along with health navigator support. The intervention will last seven days, with assessments conducted at baseline, one week post-intervention, and six months post-intervention via surveys and telephone follow-up.

The study tests the following hypotheses:

(H1) women in the wPap intervention group will achieve higher CC screening rates than the waitlist control group; (H2) the wPap group will demonstrate greater improvements in knowledge, attitudes/beliefs, self-efficacy, and intention to undergo CC screening; and (H3) the wPap group will report higher satisfaction and acceptance of the intervention compared with the waitlist control group. Findings will inform the feasibility, acceptability, and efficacy of mobile web app interventions tailored to Indigenous communities to improve CC screening.

Who Is on the Research Team?

SR

Soonhee Roh, PhD

Principal Investigator

University of South Dakota

Are You a Good Fit for This Trial?

Inclusion Criteria

Women who are self-identified AI women of the YST in SD
I am a woman between 25 and 65 years old.
I have not had a Pap or HPV test in the past few years.
See 1 more

Exclusion Criteria

I am a woman younger than 25 or older than 65.
I have been diagnosed with cervical cancer in the past.
I am up to date with my cervical cancer screening tests.
See 2 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Intervention

Participants receive a seven-day mobile web app intervention designed to promote cervical cancer screening, including daily educational modules and health navigator support.

1 week
Daily engagement via mobile app

Post-Intervention Assessment

Assessments conducted to evaluate knowledge, attitudes, self-efficacy, and intent to undergo screening.

1 week post-intervention
Surveys and telephone follow-up

Follow-up

Participants are monitored for cervical cancer screening completion and other secondary outcomes.

6 months
Telephone follow-up

What Are the Treatments Tested in This Trial?

Interventions

  • wPap Mobile Web App Intervention

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Experimental: InterventionExperimental Treatment1 Intervention
Group II: Control groupActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of South Dakota

Lead Sponsor

Trials
16
Recruited
2,000+