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Patient-centered Educational Material to Improve Colposcopy Adherence

Patient-centered Educational Material to Improve Colposcopy Adherence

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05762757
Enrollment
25
Registered
2023-03-10
Start date
2024-01-30
Completion date
2024-09-06
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Cancer Screening

Keywords

cervical cancer screening, colposcopy, patient education

Brief summary

The long-term goal is to develop, test, and disseminate a social needs navigator intervention that improves colposcopy adherence. Based on stakeholder feedback, this study addresses the need to include patient-centered educational material to the navigator program in order to improve patients' health literacy regarding cervical cancer prevention.

Detailed description

The investigators will evaluate the effectiveness of the colposcopy educational material. The investigators aim to recruit 25 newly referred colposcopy patients before their appointment, ask them to take a 5-minute test about their knowledge of colposcopy, have them view an online demo of the educational resources, and then retake the test.

Interventions

OTHERColposcopy educational material

-Will consist of a handout featuring education and information regarding colposcopies.

Sponsors

American Association of Obstetricians and Gynecologists
CollaboratorUNKNOWN
Washington University School of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 21 years or older * Abnormal cervical screen confirmed by cytology or pathology * Referred to Washington University School of Medicine (WUSM) colposcopy clinic

Exclusion criteria

* History of cervical cancer * Unable to consent

Design outcomes

Primary

MeasureTime frameDescription
Change in participant knowledge of colposcopyPrior to viewing educational material and after viewing educational material (Day 1)-9 question questionnaire that will assess patient knowledge of colposcopy

Secondary

MeasureTime frameDescription
Feasibility of educational material as measured by the Feasibility of Intervention MeasureDay 1
Acceptability of educational material as measured by the Acceptability of Intervention MeasureDay 1This is a 4-item measure of perceived intervention acceptability. Items are measured on a 5-point Likert scale (Completely disagree-completely agree). Mean score is calculated.
Appropriateness of educational material as measured by the Intervention Appropriateness MeasureDay 1This is a 4-item measure of perceived intervention appropriateness. Items are measured on a 5-point Likert scale (Completely disagree-completely agree). Mean score is calculated.
Number of participants who stated that the educational material will influence their intention to adhere to colposcopyDay 1This is a 4-item measure of perceived intervention feasibility. Items are measured on a 5-point Likert scale (Completely disagree-completely agree). Mean score is calculated.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026