Programa de mSalud para la Calidad de Vida en Supervivientes de Cáncer Colorrectal
Intervention Group
Enfermedades del colon+11
+ Enfermedad
+ Enfermedades del Sistema Digestivo
Estudio de Cuidados de Apoyo
Resumen
Fecha de inicio: 1 de septiembre de 2025
Fecha en la que se inscribió al primer participante.This study is focused on improving the quality of life for people who have survived colorectal cancer. As the number of colorectal cancer survivors grows, many face challenges in maintaining a good quality of life due to limited healthcare support. This is particularly important because colorectal cancer is one of the most common cancers worldwide. The study aims to use a mobile health program, which follows guidelines from well-respected organizations like the American Cancer Society, to provide ongoing support and resources. By doing so, the study hopes to address the gaps in current care and improve the overall well-being of survivors. Participants in this study will be divided into two groups. One group will use the new mobile health program, while the other group will continue with their usual care. This app-based program will offer education on managing symptoms, nutrition, and exercise, as well as health coaching from nurses. The study will involve 210 participants and measure their progress at different times: when they start the study, right after the program ends, and one month later. The effectiveness of the program will be analyzed using statistical methods to ensure that the results are reliable. This approach aims to provide a more comprehensive support system for colorectal cancer survivors.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 210 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Estudio de Cuidados de Apoyo
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.A partir de 18 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
Inclusion Criteria: * be 18 or older (1); * Vietnamese-speaking CRC patients who have completed active treatment and are preparing for discharge (2); * provide consent and complete questionnaires independently (3); * no metastatic and second cancers (4); * using the Android smartphone (5). Exclusion Criteria: * mental health diseases; * receiving anxiety or depression treatment or cognitive/learning problems.
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.Un solo grupo de intervención está designado en este estudio
0% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
Grupo I
Comparador ActivoObjetivos del Estudio
Objetivos Primarios
Objetivos Secundarios