Unidos Contra el VPH
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Self-sampling with urine, Self-sampling with swab, In-clinic Pap/HPV co-testing.
- Кому может быть актуально
- Состояния в реестре: Human Papilloma Virus (HPV), Cervical Cancers. Базовые параметры: 30 лет — 65 лет · Женщины.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- США
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Не всё понятно в терминах? Прочитайте наш гид для пациентов →
Официальное название
Unidos Contra el VPH: Screening Preference and Uptake of HPV Self-sampling Among Latinxs Along the US-Mexico Border
Обзор
The purpose of the Unidos Contra el VPH study is to help find options to screen, or check, for cervical cancer that individuals can do at home to help prevent and detect cervical cancer early. Usually, people get screened for cervical cancer with a Pap smear and human papillomavirus (HPV) test by a health care provider. This is not always easy for individuals who are not able to get to a clinic or feel uncomfortable having the procedure done. That is why we want to find other ways that may be easier and more comfortable for people to be screened for cervical cancer. The two main questions the study aims to answer are: 1. How do the following three cervical cancer screening methods compare for improving screening completion rates? o In-home HPV self-sampling with a vaginal swab * In-home HPV self-sampling with urine testing * In-clinic traditional Pap smear with HPV test 2. What are participant beliefs and preferences regarding these three screening methods? Participants in the study will be randomly assigned to one of three groups. This means each person has an equal chance of being placed in any group. They will also complete two surveys as part of the study. The three screening method groups are described below: Group 1: Urine Self-Sampling * Participants in this group will receive a kit with a urine sample cup to use at home, instructions explaining how to take the sample and a pre-paid mailing box to mail the urine sample to the lab. Group 2: Vaginal Swab Self-Sampling o Participants in this group will receive a kit with a vaginal swab and collection tube to use at home, instructions explaining how to take the sample and a pre-paid mailing box to mail the sample to the lab. Group 3: In-Clinic Screening * An in-clinic co-testing appointment is scheduled for a Pap smear and HPV test done together at Project Vida Health Center. By comparing these approaches, this study aims to improve access to cervical cancer screening and provide better options for those who face barriers to clinic-based screening.
Вмешательства
- Устройство Self-sampling with urine
Urine is self-collected at home using a urine sample cup. - Устройство Self-sampling with swab
A vaginal cell sample is self-collected at home using a swab and collection tube. - Устройство In-clinic Pap/HPV co-testing
Cervico-vaginal cell samples are collected by a clinician during a Pap smear/HPV co-test appointment.
Первичные конечные точки
- Comparison of Completion Rates Among Three Cervical Cancer Screening Methods [Срок оценки: Screening completion within 60 days of enrollment]
Вторичные конечные точки (1)
- Comparison of Participant Beliefs and Preferences for HPV Self-Collection Versus Clinician-Collected Samples [Срок оценки: Participants will complete surveys at two time points: baseline (at enrollment) and follow-up (within 2 weeks of screening completion).]
Критерии участия
Критерии включения
- Individuals with a cervix who are 30-65 years and have not undergone a Pap test in at least three years.
Критерии исключения
- Having had a hysterectomy or a personal history of cervical cancer.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Да
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Открытое
- Основная цель
- Скрининг
Центры проведения
США · 1 центр
- Project Vida Health Center — El Paso
Идентификаторы
NCT: NCT06825689 · CPRIT-RP240208 · STUDY00005986