Reclutando

Psychological Benefits of a Normalized Camping Experience for Children With Cancer

0 criterios cumplidosConsulta de un vistazo cómo tu perfil cumple con cada criterio de elegibilidad.
Qué se está recopilando

Recolección de datos

Recopilados desde hoy en adelante - Prospectivo
Quiénes están siendo reclutados

Pediatric Cancer

De 7 a 25 años
+8 Criterios de eligibilidad
Cómo está diseñado el estudio

Cohorte

Seguimiento de la incidencia de una enfermedad para identificar factores de riesgo y comprender su progresión a lo largo del tiempo.
Observacional
Inicio del estudio: febrero de 1983

Resumen

Patrocinador PrincipalNational Cancer Institute (NCI)
Contacto del EstudioTammara Jenkins, R.N.
Última actualización: 1 de octubre de 2025
Extraido de una base de datos validada por el gobierno.Reclamar como socio
Fecha de inicio: 15 de febrero de 1983Fecha en la que se inscribió al primer participante.

Background: * Cancer has an enormous impact on the psychological and social well-being of the family unit. The life-threatening connotations of cancer single out the ill child from his peer/family group as one who is different, and often unable to maintain a normal lifestyle. Physical sequelae of cancer and its treatment accentuate the differences between these children and their normal peers/siblings. * It is important that children with cancer be prepared to function outside of protected situations and begin to develop skills of separation and independence. For healthy children, some of these latter skills are acquired by a camping experience. Such an experience for the patient with cancer is frequently precluded by their dependence on medical facilities and the physical limitations of their activities. * The goal of this study will be to assess the short and long term benefits of the "normalized" camping experience, provided in conjunction with Special Love, Inc., on the patients and staff. In particular, we will seek to determine whether such a comprehensive experience is capable of influencing the attitudes and life experiences of patients and staff in a positive manner. Objectives: -To evaluate the impact of an enriched normalized camping experience on the quality of life of the pediatric cancer patient. In particular, attempts will be made to measure the manner in which this experience influences the child's sense of well-being and self-esteem as well as his or her relationship with parents, family, and peers. Eligibility: * Children 7-17 years of age who are currently being treated for cancer or are up to 3 years post therapy OR Young adults with cancer (YACers) 18-25 years of age who are acting as counselors at Camp Fantastic * All children/young adults will be selected for camp after careful screening by a multidisciplinary committee consisting of medical and program directors. * At the discretion of the multidisciplinary committee consisting of medical and program directors, special exceptions may be made for children with extenuating circumstances. Design: * Assessment of benefit may include interviews with children and families before, during and following camp. Observational data on the child's performance at camp will be noted. * Medical and nursing personnel will consist of staff from the Pediatric Branch at the NCI, other units within the NIH, and participating institutions. * Special Love members, the Program Director at the 4-H Center camp (site of the camp) and Pediatric Branch staff at the NCI will coordinate the camp program, taking into account the medical needs of each camper. * Every attempt will be made to provide a full agenda of age appropriate activities for the patients. * The length of the camping experience for children with cancer will be for 7 days beginning on a Sunday and extending through the following Saturday morning. Patients will be transported to the camp from the NIH Clinical Center and the Virginia hospitals by bus. Background: * Cancer has an enormous impact on the psychological and social well-being of the family unit. The life-threatening connotations of cancer single out the ill child from his peer/family group as one who is different, and often unable to maintain a normal lifestyle. Physical sequelae of cancer and its treatment accentuate the differences between these children and their normal peers/siblings. * It is important that children with cancer be prepared to function outside of protected situations and begin to develop skills of separation and independence. For healthy children, some of these latter skills are acquired by a camping experience. Such an experience for the patient with cancer is frequently precluded by their dependence on medical facilities and the physical limitations of their activities. * The goal of this study will be to assess the short and long term benefits of the "normalized" camping experience, provided in conjunction with Special Love, Inc., on the patients and staff. In particular, we will seek to determine whether such a comprehensive experience is capable of influencing the attitudes and life experiences of patients and staff in a positive manner. Objectives: -To evaluate the impact of an enriched normalized camping experience on the quality of life of the pediatric cancer patient. In particular, attempts will be made to measure the manner in which this experience influences the child's sense of well-being and self-esteem as well as his or her relationship with parents, family, and peers. Eligibility: * Children 7-17 years of age who are currently being treated for cancer or are up to 5 years post therapy OR Young adults with cancer (YACers) 18-25 years of age who are acting as counselors at Camp Fantastic and are enrolled in another NIH protocol. * All children/young adults will be selected for camp after careful screening by a multidisciplinary committee consisting of medical and program directors. * At the discretion of the multidisciplinary committee consisting of medical and program directors, special exceptions may be made for children with extenuating circumstances. Design: * Assessment of benefit may include interviews with children and families before, during and following camp. Observational data on the child's performance at camp will be collected. * Medical and nursing personnel will consist of staff from the Pediatric Oncology Branch at the NCI, other units within the NIH, and participating institutions. * Special Love members, the Program Director at the 4-H Center camp (site of the camp) and Pediatric Oncology Branch staff at the NCI will coordinate the camp program, taking into account the medical needs of each camper. * Every attempt will be made to provide a full agenda of age appropriate activities for the patients. * The length of the camping experience for children with cancer will be for 7 days beginning on a Sunday and extending through the following Saturday morning. Patients will be transported to the camp from the NIH Clinical Center and the Virginia hospitals by bus.

Título OficialPsychological Benefits of a Normalized Camping Experience for Children With Cancer 
Patrocinador PrincipalNational Cancer Institute (NCI)
Contacto del EstudioTammara Jenkins, R.N.
Última actualización: 1 de octubre de 2025
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Protocolo

Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.
Detalles del Diseño
Se reclutarán 5000 pacientesNúmero total de participantes que el ensayo clínico espera reclutar.
Cohorte
Estos estudios siguen a un grupo de personas con características comunes (como una condición o año de nacimiento) durante un periodo específico para analizar resultados de salud o exposiciones.

Cómo se seleccionan los participantes
Los participantes se seleccionan sin utilizar un método aleatorio. Pueden ser elegidos por conveniencia, acceso o disposición a participar. Este enfoque es común cuando la selección aleatoria no es práctica.
Otra forma de seleccionar participantes es mediante una muestra probabilística, donde los participantes se eligen aleatoriamente y todos tienen la misma probabilidad de ser incluidos.

Cómo se recopila la información
Los investigadores comienzan a recopilar datos desde el presente en adelante, siguiendo a los participantes a lo largo del tiempo para observar los resultados. Este enfoque ayuda a identificar cómo las exposiciones o comportamientos pueden derivar en eventos de salud futuros.Otras formas de recopilar datos
Retrospectivo
: Estos estudios utilizan historiales médicos u otros datos pasados.

Transversal
: Estos estudios recopilan datos en un momento específico.

Otros
: Algunos estudios combinan varios enfoques o utilizan diseños menos comunes, según el objetivo de la investigación.

Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios
Cualquier sexoSexo biológico de los participantes elegibles para inscribirse.
De 7 a 25 añosRango de edades de los participantes que pueden unirse al estudio.
Voluntarios sanos no permitidosIndica si personas sanas, sin la condición que se estudia, pueden participar.
Condiciones
Patología
Pediatric Cancer
Criterios
7 criterios de inclusión requeridos para participar
A discreción del comité multidisciplinario compuesto por directores médicos y de programa, se pueden hacer excepciones especiales para pacientes con circunstancias excepcionales.

Si bien se considerará el estado de salud del niño, no habrá exclusiones para: * Pacientes que estén recibiendo medicamentos o productos sanguíneos por vía intramuscular, intratecal, oral o intravenosa. * Pacientes que hayan tenido amputaciones u otros defectos físicos. * Pacientes que presenten fiebre y neutropenia al inicio o durante la semana de campamento podrán permanecer en el campamento bajo terapia antibiótica, siempre y cuando su condición se mantenga estable.

El registro de un niño, la firma del consentimiento del protocolo y la finalización de los documentos de admisión se realizan en persona, pero en circunstancias excepcionales, pueden realizarse por teléfono después de que los documentos hayan sido enviados por correo al padre/tutor. Las circunstancias excepcionales incluirían una solicitud de último momento para el campamento después de que se hayan completado las evaluaciones para el campamento en Norfolk o Richmond.

Niños de 7 a 17 años de edad que actualmente están siendo tratados por cáncer o que están hasta 5 años después de la terapia.


Un criterio de exclusión impide participar
Niños con un diagnóstico médico distinto al cáncer o sus trastornos relacionados.

Plan de Estudio

Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.
Grupos de Tratamiento
Objetivos del Estudio
2 grupos de intervención 

están designados en este estudio

0% de probabilidad 

de ser asignado al grupo placebo

Grupos de Tratamiento
Grupo I
Children 7-17 years of age who are currently being treated for cancer or are up to 5 years post therapy.
Grupo II
Young adults with cancer (YACers) 18-25 years of age acting as counselors at Camp Fantastic and are enrolled in another NIH protocol.
Objetivos del Estudio
Objetivos Primarios

Psychological benefit
Objetivos Secundarios

Psychological benefit

Centros del Estudio

Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.
Este estudio tiene una ubicación
Reclutando
National Institutes of Health Clinical CenterBethesda, United StatesVer ubicación

Reclutando
1 Centros de Estudio