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Educational Video's Impact on Knowledge Regarding Cervical Cancer Screening

Not Applicable
Completed
Conditions
Cervical Dysplasia
Human Papilloma Virus
Interventions
Other: Educational video
Registration Number
NCT05756192
Lead Sponsor
George Washington University
Brief Summary

The researchers will be conducting a prospective randomized trial where the researchers will be introducing an educational video to see whether there is an increase in knowledge scores surrounding cervical cancer, cervical cancer screening, and prevention with HPV vaccinations.

Detailed Description

The researchers are conducting a single-blinded randomized controlled trial. All patients who meet exclusion criteria will be recruited at the time of their visit where a Pap smear will be collected at an ob/gyn clinic. If patients agree to participate in the study, they will be randomized into one of two arms. A control arm or an interventional arm. The control arm just includes physician counseling regarding cervical cancer screening/prevention, while the interventional arm includes patient's watching a video on cervical cancer screening/prevention as well as physician counseling. Patient will be administered a survey before and after to assess knowledge and satisfaction scores.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
200
Inclusion Criteria
  • Female patient
  • Hispanic patients
  • Between age 21-65 y/o
  • Receiving pap smear during clinic appointment
Read More
Exclusion Criteria
  • Non-female patients
  • Non-Hispanic patients
  • Age less than 21
  • Age greater than 65
  • not receiving pap smear
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Video and physician counseling armEducational videoThis groups will complete a pre survey and will then watch the 10-minute educational video on cervical cancer screening and prevention prior to seeing their provider. Patients will then see the provider and will complete a post survey following appointment.
Primary Outcome Measures
NameTimeMethod
Pre Knowledge scoreWill be measured immediately before the appointment.

Knowledge scores regarding cervical cancer screening and prevention. This will be scored as percentage correct out of 13 questions.

Post knowledge scoreWill be measured immediately after the appointment.

Knowledge scores regarding cervical cancer screening and prevention. This will be scored as percentage correct out of 13 questions.

Secondary Outcome Measures
NameTimeMethod
Post Satisfaction scoresWill be measured immediatley after the provider visit and/or administration or video based educational tool (if randomized to the intervention line).

Satisfaction scores regarding intervention and appointment. Satisfaction questions will be scored on Likert scale from 1-5 with 5 being most satisfied and 1being the least sat

Trial Locations

Locations (1)

Stephanie Wang

🇺🇸

Washington, District of Columbia, United States

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