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Educational Material for Cervical Cancer Screening Adherence
N/A
Recruiting
Led By Lindsay M Kuroki, M.D.
Research Sponsored by Washington University School of Medicine
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up day 1
Awards & highlights
Study Summary
This trial aims to create an educational program to help patients better understand cervical cancer prevention and improve their adherence to colposcopy. #CervicalCancer
Who is the study for?
This trial is for individuals aged 21 or older who have had an abnormal cervical screening and are referred to the WUSM colposcopy clinic. It's not open to those who cannot consent or have a history of cervical cancer.Check my eligibility
What is being tested?
The study is testing patient-centered educational materials designed to improve understanding and adherence to colposcopy procedures, which are important in preventing cervical cancer.See study design
What are the potential side effects?
Since this trial involves educational material rather than medical treatment, there are no direct side effects associated with it.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ day 1
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 1
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in participant knowledge of colposcopy
Secondary outcome measures
Acceptability of educational material as measured by the Acceptability of Intervention Measure
Appropriateness of educational material as measured by the Intervention Appropriateness Measure
Feasibility of educational material as measured by the Feasibility of Intervention Measure
+1 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: Colposcopy educational materialExperimental Treatment1 Intervention
Participants will complete a 9-question quiz that will assess knowledge of colposcopy. They will then view the colposcopy educational material and answer the same 9-question quiz to assess their knowledge of colposcopy. Participants will complete the Acceptability Intervention Measure, the Intervention Appropriateness Measure, and the Feasibility of Intervention Measure. Participants will also be asked whether the educational material influences their intention to adhere to colposcopy.
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Who is running the clinical trial?
American Association of Obstetricians and GynecologistsUNKNOWN
Washington University School of MedicineLead Sponsor
1,937 Previous Clinical Trials
2,299,677 Total Patients Enrolled
Lindsay M Kuroki, M.D.Principal InvestigatorWashington University School of Medicine
2 Previous Clinical Trials
177 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I have had cervical cancer in the past.I am unable to give consent by myself.I am 21 years old or older.
Research Study Groups:
This trial has the following groups:- Group 1: Colposcopy educational material
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Has recruitment begun for this experiment?
"Accessible information on clinicaltrials.gov reveals this study is no longer open for recruitment. The trial was initially posted in November 30th 2023, and the most recent update was issued on March 6th of last year. However, there are still 317 other medical studies actively searching for patients at present."
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