- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02151032
Using Multimedia Approaches to Communicate Probabilities in Patient Decision Aids for Low-Literacy Populations: Randomized Trial
Descripción general del estudio
Estado
Condiciones
Descripción detallada
If you agree to take part in this study, you will be randomly assigned (as in a roll of dice) to 1 of 3 study groups. Neither you nor the study staff will be able to choose which group you will be in:
- If you are in Group 1, you will read a booklet about colorectal cancer screening tests. While reading the booklet, you will also listen to an audio CD that will narrate the booklet.
- If you are in Group 2, you will watch a video with non-moving images about colorectal cancer screening tests on an iPad.
- If you are in Group 3, you will watch a video with animated images about colorectal cancer screening tests on an iPad.
You will complete questionnaires before and after viewing the program that will contain questions about:
- Your age and what language you speak
- Your math and reading comprehension
- Your knowledge of colorectal cancer and colorectal cancer screening
- Your thoughts about colorectal cancer screening
- Your opinions about this study, and
- How well you understand the booklet/video you view as part of this study
It will take about 1 hour to complete all the questionnaires. In total, the study will take about 1 ½ to 2 hours to complete. After you have completed the questionnaires, your participation in the study will be over.
This is an investigational study.
Up to 201 people will take part in this multicenter study. Up to 67 will be enrolled at MD Anderson.
Tipo de estudio
Inscripción (Actual)
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Texas
-
Houston, Texas, Estados Unidos, 77030
- University of Texas MD Anderson Cancer Center
-
Houston, Texas, Estados Unidos, 77042
- Literacy Advance of Houston
-
Houston, Texas, Estados Unidos, 77035
- Bethel's Heavenly Hands
-
Houston, Texas, Estados Unidos, 77071
- Ephiphany Community Health Outreach Services
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria:
- Men and women 45 to 75 years of age.
- Participant must speak English.
Exclusion Criteria:
1) Self-reported diagnosis of colon cancer.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
|---|---|
|
Colorectal Cancer Screening Booklet + Audio CD
Participants read the booklet about colorectal cancer screening tests, and listen to an audio CD that will narrate the booklet.
Questionnaire completion before and after viewing the program.
|
Participants read a booklet about colorectal cancer screening tests.
Otros nombres:
Participants listen to an audio CD that will narrate the colorectal cancer screening tests booklet.
Questionnaire completion before and after viewing the program.
Otros nombres:
|
|
Video with Non-Moving Images on iPad
Participants watch a video with non-moving images about colorectal cancer screening tests on an iPad.
Questionnaire completion before and after viewing the program.
|
Questionnaire completion before and after viewing the program.
Otros nombres:
Participants watch a video with non-moving images about colorectal cancer screening tests on an iPad.
|
|
Video with Animated Images on iPad
Participants watch a video with animated images about colorectal cancer screening tests on an iPad.
Questionnaire completion before and after viewing the program.
|
Questionnaire completion before and after viewing the program.
Otros nombres:
Participants watch a video with animated images about colorectal cancer screening tests on an iPad.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Gist and Verbatim Knowledge for a Colorectal Cancer Screening Program
Periodo de tiempo: 1 day
|
The fixed effects analysis of variance (ANOVA) will utilize a factorial design with two factors: content presentation type (standard, animated, interactive) and numeracy status (high and low based on US population scores).
Main dependent measures are gist and verbatim knowledge.
Gist and verbatim knowledge scores (0-100) looked at separately as well as combined.
|
1 day
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Robert Volk, PHD, M.D. Anderson Cancer Center
Publicaciones y enlaces útiles
Publicaciones Generales
- Housten AJ, Kamath GR, Bevers TB, Cantor SB, Dixon N, Hite A, Kallen MA, Leal VB, Li L, Volk RJ. Does Animation Improve Comprehension of Risk Information in Patients with Low Health Literacy? A Randomized Trial. Med Decis Making. 2020 Jan;40(1):17-28. doi: 10.1177/0272989X19890296. Epub 2019 Dec 3.
- Housten AJ, Lowenstein LM, Hoover DS, Leal VB, Kamath GR, Volk RJ. Limitations of the S-TOFHLA in measuring poor numeracy: a cross-sectional study. BMC Public Health. 2018 Mar 27;18(1):405. doi: 10.1186/s12889-018-5333-9.
Enlaces Útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
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
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 2011-0632
- 0619-1 (Otro número de subvención/financiamiento: Foundation for Informed Medical Decision Making)
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. .