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Text Message Reminders for Cervical Cancer Screening
Study Summary
This trial will test whether text message reminders can help women keep up with recommended cervical cancer screenings.
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- You are a woman.If you are a transwoman and have had surgery to remove your cervix, you cannot participate in this trial.
- Group 1: In-person Treatment
- Group 2: in-person control
- Group 3: Self-Administered Control
- Group 4: Self-Administered Treatment
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- 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
Does this research endeavor currently have capacity for new participants?
"Affirmative, the information hosted on clinicaltrials.gov reveals that this examination is currently seeking participants. The investigation was initially posted in December of 2020 and most recently updated in May 2022- with a goal of recruiting 1460 individuals from 2 sites."
Who qualifies to partake in this research initiative?
"For this research undertaking, 1460 participants aged 21 - 65 years old and of the female gender will be accepted. Additionally, these individuals must have decisional capacity to consent to participation in order to qualify for inclusion."
Does this research trial accommodate geriatric volunteers aged 75 or below?
"The eligibility requirements for this clinical investigation necessitate that candidates are between the ages of 21 and 65."
How many subjects have participated in this research endeavor?
"Confirmed. Clinicaltrials.gov data shows that this medical trial, initiated on December 3rd 2020, is currently looking for volunteers to join the study. Specifically, 1460 participants are needed from 2 separate sites."
Who else is applying?
What state do they live in?
How old are they?
What site did they apply to?
What portion of applicants met pre-screening criteria?
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