- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT04093401
The VIDYA Study-designed to Determine if Patients With a History of Basal Cell Carcinoma Are More Inclined to Return for Follow-up if Their Risk of a Subsequent Basal Cell Carcinoma is Quantitated.
An Open-Label, Single Blind Study of How Knowledge of Risk of Subsequent Basal Cell Carcinoma Affects Compliance With Requested Follow-Up in Patients With First Basal Cell Carcinoma
While current guidelines call for annual follow-up for patients with a history of basal cell carcinoma, compliance with these guidelines is imperfect. It is hypothesized that if patients are informed of the quantitative risk of a subsequent basal cell carcinoma based on individualized risk factors, the compliance rate for follow-up will improve.
The primary objective of this study is to assess one-year compliance with requested follow-up for patients with recent history of basal cell carcinoma, among those who receive standard sun avoidance counseling and request for follow-up compared to those who receive, in addition, an estimate of their mathematical risk of a subsequent basal cell carcinoma based on individualized risk factors.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
This is an open-label, single-blind study to evaluate the effect of informing subjects of their individualized risk of a subsequent basal cell carcinoma on proportion of subjects who achieve compliance with requested follow-up with a dermatology healthcare provider, defined as in-person follow-up within 365 days following diagnosis of initial basal cell carcinoma.
Subjects will be randomized 1:1 to "intervention" (knowledge of individualized risk) or "control" (lack of awareness of individualized risk). Investigators will be aware of the modelled risk of a subsequent basal cell carcinoma for all subjects, but only subjects randomized to the "intervention" arm will be informed of their modelled risk. All subjects will receive standard sun avoidance counseling and will be requested to follow-up no later than 365 days from initial basal cell carcinoma diagnosis.
Tipo de estudio
Fase
- No aplica
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Age 18 years or older
- Diagnosed with at least one Basal Cell Carcinoma within 30 days prior to enrollment
- Able and willing to answer all questions accurately in the Individualized Risk Assessment
Exclusion Criteria:
- History of Basal Cell Carcinoma 31 or more days prior to enrollment
- Solid Organ Transplant Recipient
- History of Immunodeficiency (e.g., HIV infection, AIDS, genetic immunodeficiency
- Prisoner
- Psychiatric inpatients or people who are institutionalized
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Cuidados de apoyo
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
---|---|
Sin intervención: Control
Subjects will be assigned to the control arm if their subject ID is an odd number.
Control arm subjects will not receive counseling for individualized risk assessment for developing a second basal cell carcinoma.
|
|
Experimental: Individualized risk assessment
Subjects will be assigned to the intervention arm (i.e., informed of their individualized risk assessment) if their subject ID is an even number.
Subjects in the intervention arm will be informed of their estimated 1-year, 3-year, and 5-year risk of developing a second basal cell carcinoma.
|
Individualized risk assessment of developing a second basal cell carcinoma
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Number of participants who have a followup second skin exam by a dermatologist within 1 year of diagnosis of their first basal cell carcinoma (BCC)
Periodo de tiempo: up to 13 months
|
Number of participants who have a followup second skin exam by a dermatologist within 1 year of diagnosis of their first basal cell carcinoma (BCC)
|
up to 13 months
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Frequency of sunscreen use when out in sun
Periodo de tiempo: up to 13 months
|
Frequency of sunscreen use when out in sun Participants will be instructed to use sunscreen on a daily basis during April - October.
Regularity of sunscreen use will be queried during sunny parts of the year (spring to fall).
Frequency of sunscreen use will be measured as daily use during the months of April - October
|
up to 13 months
|
Frequency of sunburns within the past year
Periodo de tiempo: up to 13 months
|
Frequency of sunburns within the past year
|
up to 13 months
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Robert J Glinert, MD, clinical professor
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Anticipado)
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- UW19002
- A534300 (Otro identificador: UW Madison)
- 2019-0077 (Otro identificador: Institutional Review Board)
- SMPH/DERMATOLOGY/DERMATOLOG (Otro identificador: UW Madison)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .
Ensayos clínicos sobre Carcinoma de células basales
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University Medical Center GroningenFresenius Medical Care North AmericaTerminadoGlomerulonefritis Anti-Membrana Basal GlomerularPaíses Bajos
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Mårten SegelmarkHansa Biopharma ABTerminadoEnfermedad por anticuerpos contra la membrana basal glomerularAustria, Chequia, Dinamarca, Francia, Suecia
Ensayos clínicos sobre individualized risk assessment
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Centre Francois BaclesseTerminado
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University of CataniaUniversity of Roma La Sapienza; Hospital General Universitario Santa Lucia; Klinik...Aún no reclutandoEsclerosis múltipleItalia
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University Hospital, CaenDesconocido