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Набор скоро начнётся NCT07632963

Addressing HPV Vaccine Hesitancy by Co-Designing a Digital Health Intervention

Без фазы С лечением HPV Vaccine Acceptance Vaccine Decision Making HPV Vaccination

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: HPV-Kompassen.
Кому может быть актуально
Состояния в реестре: HPV, Vaccine Acceptance, Vaccine Decision Making, HPV Vaccination. Базовые параметры: Без ограничений · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Список центров уточняется — проверьте первичный протокол.
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Официальное название

HPV-Kompassen: a Mixed-Methods Single-Arm Cluster Feasibility Study of a Co-Designed Web-Based Intervention To Strengthen HPV Vaccine Confidence and Uptake in Stockholm, Sweden

Обзор

This study looks at a digital platform that supports HPV vaccination in schools. The goal is to see if it is useful, easy to use, and practical in real school settings, especially in areas where fewer people get vaccinated. Researchers will give Year 5 pupils (aged 11-12) and their parents or caregivers access to the platform. It provides clear, trusted information about the HPV vaccine for young people, parents, and school nurses. The aim is to make the vaccine easier to understand and to help answer any questions or concerns. After using the platform, participants will be asked to share their thoughts.

Вмешательства

  • Поведенческое HPV-Kompassen
    HPV-Kompassen is a co-designed, web-based platform that provides tailored and synthesised information with the aim of strengthening confidence in and uptake of the HPV vaccine.

Первичные конечные точки

  • Feasibility of implementation: Acceptability, appropriateness and feasibility of implementation [Срок оценки: Shortly after the intervention period (i.e., 'end of treatment') at 7 months.]
  • Feasibility of implementation: Acceptability, appropriateness and feasibility of implementation [Срок оценки: Shortly after the intervention period (i.e., 'end of treatment') at 7 months.]
  • Acceptability of intervention: Intervention delivery strategy [Срок оценки: Throughout the intervention period (i.e., months 0-7).]
  • Acceptability of intervention: Usability of intervention [Срок оценки: Immediately after the intervention period (i.e., 'end of treatment') at 7 months.]
  • Acceptability of intervention: Perceptions of intervention [Срок оценки: Shortly after the intervention period (i.e., 'end of treatment') at 7 months.]
  • Acceptability of intervention: Intervention engagement [Срок оценки: Throughout the intervention period (i.e., months 0-7).]
  • Acceptability of intervention: Intervention engagement [Срок оценки: End of intervention period (i.e., 'end of treatment') at 7 months.]
  • Feasibility of trial protocol: Feasibility of recruitment [Срок оценки: From start of school enrollment (i.e., pre-intervention) and throughout the intervention period (i.e., months 0-7).]
  • Feasibility of trial protocol: Participant retention [Срок оценки: From school enrollment (i.e., 'baseline') and throughout the intervention period (i.e., months 0-7).]
  • Feasibility of trial protocol: Feasibility of data collection methods [Срок оценки: Shortly after the intervention period (i.e., 'end of treatment') at 7 months.]

Критерии участия

We will aim to recruit 6-8 compulsory schools in Stockholm County to serve as clusters.

All Year 5 pupils and their caregivers in the study schools are invited.

Критерии включения

  • The school provides education to pupils in school year 5 and is scheduled to be open throughout the pilot trial period
  • The school is located in an area with HPV vaccine uptake <85.2% (the Stockholm regional average)
  • The head principal and school nurse both consent to participate
  • The school has the capacity to implement the intervention

Критерии исключения

  • Failure to meet the inclusion criteria

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Другое

Центры проведения

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT07632963 · 2023-00331

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗