Video-Tumorboard PLUS
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
- Это наблюдательное исследование: исследуемое лечение участникам по протоколу не назначают.
- Кому может быть актуально
- Состояния в реестре: Malignant Melanoma, Telemedicine. 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
- Германия
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Обзор
In weekly expert meetings for oncological diagnostics and therapy, known as tumor boards, individual therapy recommendations are developed for cancer patients. By further developing and optimizing the CCCs' video tumor boards, initially using skin cancer as an example, we want to ensure that more patients can benefit from the expertise of several specialist disciplines and innovations - regardless of where they live.
Первичные конечные точки
- Presentation of external patients in the video-tumorboard [Срок оценки: Day 365]
Вторичные конечные точки (5)
- Increase in the proportion of external patients invited to a clinical study [Срок оценки: Day 365]
- Adherence to tumorboard recommendations for external patients [Срок оценки: Up to two weeks after inclusion]
- Offer of supportive therapies by the comprehensive cancer center [Срок оценки: Up to two days after inclusion]
- Duration of the transmission of the tumorboard recommendations [Срок оценки: Up to two weeks after inclusion]
- "Time to integration" into palliative care [Срок оценки: Once per patient within two weeks after transmission of the tumorboard recommendation if applicable]
Критерии участия
Критерии включения
- The study includes adult, external patients who, according to the certification requirements of the German Cancer Society, should be presented to the CCCs in a tumor board .
Inclusion criteria for patients:
- Minimum age 18 years
- Consent to participate in the study (signing of patient consent) should be presented in vTB+ according to the doctor, based on the disease/diagnosis, especially in the case of:
- Malignant melanoma from stage IIB
- Malignant melanoma and stage shift/recurrence o Extracutaneous melanoma o Cutaneous lymphoma from stage Ib o Problem cases with malignant, epithelial tumors (BCC, SCC) with interdisciplinary issues, e.g. complicated localization, extension/ infiltration (e.g. Ulcus rodens, Ulcus terebrans), metastasized tumors, immunosuppressed patients o all rare malignant skin tumors (including Merkel cell carcinoma, DFSP, MFH, leiomyosarcoma, S., Kaposi's sarcoma, angiosarcoma), regardless of stage o severe side effects from drug-based tumor therapy • is an external patient: An external patient is someone who receives tumor therapy exclusively or in co-treatment in the branch or in an external clinic (in distinction to patients without prior treatment for initial presentation at the CCC) . This also applies to patients who are only seen once at the vTB.
In this case, revenue/cost aspects and the DKG requirement are ignored. This means that so-called external patients can also be treated at the center, including initiation of therapy. The decisive factor is the presentation of the external patient (personal presentation of the external patients is not mandatory) and that external co-treaters are consistently informed and involved.
Inclusion criteria for external doctors:
- has a medical license
- has dermatological patients who are eligible to be presented in the vTB+
Критерии исключения
Patients will be excluded from the study if they meet the following criteria:
- Linguistic or other limitations (such as dementia) that prevent independent consent to the privacy policy.
- No consent to participate in the study (patient consent) or withdrawal of consent during the course of the study In addition, external physicians will be excluded from the study if no joint cooperation agreement can be negotiated and signed.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Модель наблюдения
- Когортное
Центры проведения
Германия · 3 центра
- Abteilung für Integrierte Onkologie - CIO Bonn, Universitätsklinikum Bonn — Bonn
- Nationales Centrum für Tumorerkrankungen Klinik u. Poliklinik für Dermatologie, Universitä — Dresden
- Westdeutsches Tumorzentrum Münster, Universitätsklinikum Münster — Münster
Идентификаторы
NCT: NCT06980740 · BO ff (Multi)-EK-16012025 · 2025-275-b-S