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Набор скоро начнётся NCT07531277

Developing Resource Interventions for Healthcare Professionals and Patients to Improve Knowledge About Fertility in Primary Ciliary Dyskinesia

Без фазы С лечением Primary Ciliary Dyskinesia (PCD) Fertility Pregnancy Health Information Exchange

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: Online educational resource, Toolkit for healthcare professionals.
Кому может быть актуально
Состояния в реестре: Primary Ciliary Dyskinesia (PCD), Fertility, Pregnancy, Health Information Exchange. Базовые параметры: от 18 лет · 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 →
Официальное название

REproductive Health in PRimary Ciliary Dyskinesia: Developing User-informed Clinical and Educational Resources (REPRoDUCE)

Обзор

This project will involve working with people with PCD and medical professionals to develop resources that will help patients and the people providing their care to better understand fertility and pregnancy safety in people with this condition.

Подробное описание

The study investigators will co-develop an online educational animation and text resource for patients and the public about PCD and fertility and pregnancy.

Development of patient resource:

The study investigators will conduct workshops with a group of approximately ten people including additional PPI representatives (adults with lived experience of PCD), representatives from PCD Support UK and medical professionals specialising in PCD. In stage 1 of the resource development, the study investigators will conduct an online workshop to identify priorities for information for inclusion in the resource. In stage 2 the study investigators will create a resource prototype based on the information gained in stage 1. In stage 3 the study investigators will conduct and record 1:1 online think aloud interviews to capture real-time reactions and gain evaluation of the resource prototype to identify areas for improvement. In stage 4, the study investigators will make further resource modifications. In stage 5 the intervention will be tested in a sample of men and women with PCD (n=10). The study investigators will then conduct an online quiz to measure pre- and post- resource use knowledge about PCD, fertility and pregnancy, and collect suggestions for improvement via a survey form. Feedback from stage 5 will be incorporated into the final resource prior to dissemination.

The resource will be translated into non-English languages spoken in the UK to aid inclusion of a wider audience.

Co-development of toolkit for medical professionals:

The study investigators will co-develop an online educational toolkit for medical professionals about fertility and pregnancy in patients with PCD. The study investigators will utilise the same group of approximately ten people including PPI representatives, representatives from PCD Support UK and medical professionals specialising in PCD as above. The study investigators will follow the above stages 1-4 for development of the toolkit. In stage 5, the study investigators will test the intervention in a sample of non-PCD specialists (n=10). During this stage an online quiz will be conducted to measure pre- and post- toolkit use knowledge about PCD, fertility and pregnancy, and collect suggestions for improvement via a survey form. Feedback from stage 5 will be incorporated into the final resource prior to dissemination.

Вмешательства

  • Другое Online educational resource
    Co-developed educational resource for patients
  • Другое Toolkit for healthcare professionals
    co-developed online educational toolkit for healthcare professionals

Первичные конечные точки

  • A resource for patients and a toolkit for medical professionals [Срок оценки: Duration of study (up to 3 years)]

Критерии участия

Критерии включения

  • Aged 18 years or older
  • 'Highly likely' or confirmed diagnosis of Primary Ciliary dyskinesia, or being a healthcare professional, or representative from a stakeholder group e.g. patient led charity
  • Able to understand and willing to sign the informed participant consent prior to participation

Критерии исключения

  • Unwilling to participate in the study
  • Not meeting inclusion criteria
  • Unable to understand or unwilling to sign the informed participant consent prior to participation

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Нерандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Другое

Центры проведения

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT07531277 · 107544

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗