Nurse-led Proactive Telephone Follow-up With Patients After Completion of Primary Cancer Treatment
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: Proactive nurse-led telephone follow-up.
- Кому может быть актуально
- Состояния в реестре: Breast Cancer, Colorectal Cancer, Prostate Cancer. 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
- Швеция
- 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
How Are You Getting on? Nurse-led Proactive Telephone Follow-up With Patients After Completion of Primary Cancer Treatment Increases Their Sense of Security and Well-being
Обзор
The goal of this randomized study is to test and evaluate nurse-led telephone follow-up intervention in patients primarily curatively treated for breast cancer, colorectal cancer, and prostate cancer. The main question aims to answer: Does this nurse-led telephone follow-up improve patients' quality of life? Participants in both groups will be asked to fill in questionnaires regularly. The intervention group will get a telephone follow-up at predetermined intervals, while the control group will get the care as usual.The investigators will compare intervention and control groups to see if predetermined regular nurse-led telephone follow-up improves quality of life.
Подробное описание
The hypothesis is that nurse-led telephone follow-up will improve the quality of life in patients primarily curatively treated for breast cancer, colorectal cancer, and prostate cancer.
Participants in both groups will respond to a survey regularly during one year from inclusion. The intervention group will get a telephone follow-up at predetermined intervals (1, 3, 6, 9, 12 months) while the control group will get the care as usual. The usual care means that no proactive support is offered to patients from health care while they wait for follow-up, but patients are of course allowed to contact health care if they needed.
Participants in both groups are asked to respond on a survey concerning their quality of life, feelings of anxiety and depression, perception of illness, and experienced symptoms and discomfort regarding to cancer. Additionally, the number of visits at the health care during the waiting for follow-up will be collected from both group.
Вмешательства
- Поведенческое Proactive nurse-led telephone follow-up
An intervention nurse call the patients regularly with predetermined intervals and give support
Первичные конечные точки
- Patients' reported Quality of life [Срок оценки: Baseline, 3 months, 6 months and 12 months from inclusion]
Вторичные конечные точки (6)
- Patients' reported anxiety and depression [Срок оценки: Baseline, 3 months, 6 months and 12 months from inclusion]
- Patients' reported quality [Срок оценки: Baseline, 3 months, 6 months and 12 months from inclusion]
- Patients' perceptions of illness [Срок оценки: Baseline, 3 months, 6 months and 12 months from inclusion]
- Patients' experiences of breast cancer related to body image, sexual functioning, systemic therapy side effects and symptoms [Срок оценки: Baseline, 3 months, 6 months and 12 months from inclusion]
- Patients' experiences of colorectal cancer related to symptoms and side effects of treatment and diagnosis. [Срок оценки: Baseline, 3 months, 6 months and 12 months from inclusion]
- Patients' experiences of prostata cancer related to symptoms and side effects of treatment and diagnosis. [Срок оценки: Baseline, 3 months, 6 months and 12 months from inclusion]
Критерии участия
Критерии включения
- Being primarily curatively treated for breast, colorectal-, or prostate cancer
Критерии исключения
- no adjuvant treatment
- no cognitive impairment
- no known alcohol or other misuse
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
- Двойное слепое
- Основная цель
- Поддерживающая терапия
Центры проведения
Швеция · 1 центр
- Norrlands universitetssjukhus — Umeå
Идентификаторы
NCT: NCT06223022 · Department of Nursing