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Идёт набор NCT07456566

Developing a Self-Management Intervention to Improve Health Outcomes for Patients With Inflammatory Bowel Disease

Без фазы С лечением Inflammatory Bowel Diseases Ulcerative Colitis Crohn Disease

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: Digital self-management program, Standard Care.
Кому может быть актуально
Состояния в реестре: Inflammatory Bowel Diseases, Ulcerative Colitis, Crohn Disease. 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
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Developing a Self-Management Intervention to Improve Health Outcomes for Patients With Inflammatory Bowel Disease: Part 3 Pilot Trial

Обзор

This research is studying whether changing an individual's behaviors may have an impact as a treatment or outcome for inflammatory bowel disease. This research will increase the understanding of the role of a self-management program in improving health and health-related quality of life for patients with inflammatory bowel disease. The study team hypothesizes: * the study will achieve a recruitment rate of 10 participants every 3 months * 70% participant retention at 24 weeks * 70% outcome data collection * 70% intervention completion * high acceptability

Вмешательства

  • Поведенческое Digital self-management program
    Participants will receive this 24-week digital self-management program that was developed for patients with inflammatory bowel disease in addition to standard care. The program will be accessed through the web or a mobile device and will include different modules that will help support in managing participant's symptoms and disease both in the short-term as well as helping to build habits and skills to support participants in managing disease long-term. Participants are not required to use the s
  • Поведенческое Standard Care
    Participants will have baseline assessment of symptoms both based on self-report and a clinician's assessment, and review the electronic health record for standard of care inflammatory biomarker measurements. In addition, questionnaires will be collected and visit completed at 8,12, and 24-week follow-ups.

Первичные конечные точки

  • Participant recruitment rate [Срок оценки: 2 years (during the recruitment period)]
  • The proportion of enrolled participants that complete the study without dropout [Срок оценки: 24 weeks]
  • The proportion of study assessments completed by the participant [Срок оценки: 24 weeks]
  • Qualitative interviews - self-management program group [Срок оценки: 24 weeks]
Вторичные конечные точки (3)
  • Theoretical Framework of Acceptability (TFA) [Срок оценки: 24 weeks]
  • Treatment Acceptability Adherence Scale (TAAS) [Срок оценки: 24 weeks]
  • Qualitative interviews - self-management program group [Срок оценки: 24 weeks]

Критерии участия

Критерии включения

  • Diagnosis of Inflammatory Bowel Disease (IBD) based on conventional clinical, endoscopic, and histopathological criteria, clinically active IBD
  • Impaired health-related quality of life
  • Clinically active IBD will be indicated by both a modified Harvey Bradshaw Index (HBI) ≥5 for Crohn's disease (CD) or a Simple Clinical Colitis Activity Index (SCCAI) ≥3 for ulcerative colitis (UC)
  • Fecal calprotectin > 250 microgram (ug/g)
  • Impaired IBD-specific health-related quality of life will be defined as a Short IBD Questionnaire score ≤ 60

Критерии исключения

  • Unable to speak and read English
  • Unable to access the internet regularly by phone or web as this will impair participants ability to engage with the intervention components
  • Have an ileostomy, colostomy, ileoanal pouch, or ileorectal anastomoses
  • Are planned for imminent surgery
  • Have short bowel syndrome
  • Uncontrolled medical or psychiatric disease

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

США · 1 центр
  • University of Micigan — Ann Arbor

Идентификаторы

NCT: NCT07456566 · HUM00246865 · 1K23DK136928-01A1

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗