Patient Reported Outcomes Burdens and Experiences - Phase 3
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: Quality of life measure (survey).
- Кому может быть актуально
- Состояния в реестре: Hemophilia, Chronic Disease. 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
- Канада
- 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
Patient Reported Outcomes Burdens and Experiences (PROBE) - Phase 3 - Longitudinal Data Collection
Обзор
The PROBE Phase-3 study will collect data on patient reported outcomes, burdens, and experiences in patients living with hemophilia. The investigators will perform comparisons among countries, within country over time, within country against national normative data.
Подробное описание
BACKGROUND
The PROBE questionnaire is a tool for the assessment of patient-reported outcome, burdens and experiences. Until now, it has been used in persons living with hemophilia (PWH) and healthy controls. In phase 1 of the study, the investigators developed the questionnaire. In phase 2 of the study, the investigators evaluated the reliability, reproducibility, responsiveness, and costs of PROBE. The tool has been tested across 21 countries and it has been shown that PROBE is a valid questionnaire for the evaluation of patient reported outcomes (PROs) in PWH and control populations. The questionnaire is available in 11 languages (with 20 localized versions worldwide), and another 17 languages and 45 more localizations are in the process of development.
CURRENT STUDY and FUTURE DIRECTIONS
Phase 3 is the natural prosecution of the project. In this phase, the investigators aim at maintaining the capacity to collect data on PROBE, and the infrastructure will also be modified in order to allow for longitudinal collection of PROBE data (in previous phases, the investigators only collected anonymized data).
The objective of the study is to compare data on PROBE between countries, within-countries over time, and within-countries against national normative data. Reports will be produced every 2 years. Data collected during phase 2 of the study will also be used.
At the same time, the research framework will have the potential for:
* Expanding country participation within existing and new regions. * Integrating the PROBE questionnaire in clinical trials, longitudinal studies, health technology assessment studies, routine clinical care, and registries. * Using PROBE in new countries * Testing the performance of the PROBE questionnaire in new patient populations
INVESTIGATION TEAM
Principal Investigator:
1. Mark Skinner JD, Institute for Policy Advancement Ltd. (US)
Co-Investigators: 2. Alfonso Iorio MD Ph.D. FRCPC, McMaster University, Department of Clinical Epidemiology and Biostatistics (Canada) 3. Randall Curtis MBA, Factor VIII Computing (US) 4. Neil Frick MS, National Hemophilia Foundation (US) 5. Michael Nichol Ph.D., University of Southern California, School of Policy and Planning Development (US) 6. Declan Noone, Irish Hemophilia Society (Ireland) 7. David Page, Canadian Hemophilia Society (Canada) 8. Jeff Stonebraker Ph.D., North Carolina State University Poole College of Management (US) 9. Brian O'Mahoney, Irish Hemophilia Society (Ireland) 10. Chatree Chai-Adisaksopha, MD MSc.
Вмешательства
- Другое Quality of life measure (survey)
The QoL tool is a questionnaire
Первичные конечные точки
- Between-countries variability of the PROBE score [Срок оценки: 2 years]
Вторичные конечные точки (2)
- Within-countries variability of the PROBE score [Срок оценки: 2 years]
- Within-countries comparison of the PROBE score in PWH against national normative data [Срок оценки: 2 years]
Критерии участия
Критерии включения
- PWH will be recruited through national hemophilia patient organizations utilizing their existing membership rosters, social media outlets and meetings / events. The investigators are not proposing a pre-determined method of PWH recruitment. They will utilize the information acquired in the workshop and take-home project to inform best practice in recruitment methodology for the study. The investigators may consider requesting different countries test different PWH recruitment strategies to test reproducibility.
In the future, the questionnaire might also be administered to patients with other chronic conditions.
Критерии исключения
- Disease severity and Age bands or age limits (e.g. ≥ Age 18) may be utilized to narrow the study population.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Модель наблюдения
- Когортное
Центры проведения
Канада · 1 центр
- McMaster University — Hamilton
Публикации
- Skinner MW, Chai-Adisaksopha C, Curtis R, Frick N, Nichol M, Noone D, O'Mahony B, Page D, Stonebraker JS, Iorio A. The Patient Reported Outcomes, Burdens and Experiences (PROBE) Project: development and evaluation of a questionnaire assessing patient reported outcomes in people with haemophilia. Pilot Feasibility Stud. 2018 Feb 27;4:58. doi: 10.1186/s40814-018-0253-0. eCollection 2018. PMID 29497561
Идентификаторы
NCT: NCT03549858 · PROBE-3