Post-Op Quality of Life After Colorectal Surgery
12 de diciembre de 2014 actualizado por: Conor Delaney, MD, PhD, University Hospitals Cleveland Medical Center
Postoperative Quality of Life: Development and Assessment of a Novel Tool to Assess Quality of Life Following Colorectal Surgery
The purpose of this study is to produce a user-friendly tool- in the form of a questionnaire - to accurately assess early quality of life in patients after abdominal colorectal surgery from the first day after surgery to 6 months after.
The study will also compare this questionnaire to the other currently available assessment tools.
Patients are invited to participate if they are undergoing abdominal colorectal surgery at University Hospitals of Cleveland.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Descripción detallada
The purpose of this study is to produce a user-friendly tool to accurately assess early quality of life in postoperative patients following abdominal colorectal surgery in the early postoperative period (from surgery to 6 months) that is practical for routine application.
The study will also compare this tool to the current available tools, namely the Short Form (SF-36), the short form inflammatory bowel disease questionnaire (IBDQ), the Cleveland Clinic Global Quality of Life (CGQOL).
Patients will be invited to participate if they are undergoing abdominal colorectal surgery at University Hospitals of Cleveland.
Tipo de estudio
De observación
Inscripción (Actual)
100
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
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Ohio
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Cleveland, Ohio, Estados Unidos, 44106
- University Hospitals of Cleveland
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
18 años a 85 años (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Todos
Método de muestreo
Muestra no probabilística
Población de estudio
Patients scheduled to undergo laparscopic or open procedures from the Deopartment of Surgery at University Hospitals of Cleveland.
Descripción
Inclusion Criteria:
- Subjects who are 18 years of age and older
- Subjects of either sex
- Subjects who will undergo any colorectal abdominal surgery at University Hospitals of Cleveland
- Subjects who agree to participate in the study program and provide written informed consent
- Diagnoses of Crohn's disease, ulcerative colitis, rectal or colon cancer, colon or rectal polyps and diverticulitis
Exclusion Criteria:
- Patients in the middle of three part surgery or had recent surgery (i.e., back for stoma closure for J-pouch)
- Patients with diagnosis of rectal prolapse, condyloma or any other condition that cannot be performed abdominally with an open or laparoscopic procedure
- Patient who have undergone major surgery within the month prior to this colorectal surgery
- Pregnant women, minors, psychiatric patients and prisoners
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Evaluate the quality of life in patients with abdominal wall hernias using a user-friendly survey that is designed specifically for this population of patients.
Periodo de tiempo: 1 month to 1 hour prior to surgery
|
The aim of this study is to evaluate the quality of life in patients with abdominal wall hernias using a user-friendly survey that is designed specifically for this population of patients.
We would like to use this survey to elucidate how quality of life of the patient is changed with the presence of an abdominal wall hernia.
|
1 month to 1 hour prior to surgery
|
|
Evaluate the quality of life in patients with abdominal wall hernias using a user-friendly survey that is designed specifically for this population of patients.
Periodo de tiempo: 2 weeks post operatively
|
The aim of this study is to evaluate the quality of life in patients with abdominal wall hernias using a user-friendly survey that is designed specifically for this population of patients.
We would like to use this survey to elucidate how quality of life of the patient is changed with the presence of an abdominal wall hernia.
|
2 weeks post operatively
|
|
Evaluate the quality of life in patients with abdominal wall hernias using a user-friendly survey that is designed specifically for this population of patients.
Periodo de tiempo: 4 weeks post operatively
|
The aim of this study is to evaluate the quality of life in patients with abdominal wall hernias using a user-friendly survey that is designed specifically for this population of patients.
We would like to use this survey to elucidate how quality of life of the patient is changed with the presence of an abdominal wall hernia.
|
4 weeks post operatively
|
|
Evaluate the quality of life in patients with abdominal wall hernias using a user-friendly survey that is designed specifically for this population of patients.
Periodo de tiempo: 6 months post-operatively
|
The aim of this study is to evaluate the quality of life in patients with abdominal wall hernias using a user-friendly survey that is designed specifically for this population of patients.
We would like to use this survey to elucidate how quality of life of the patient is changed with the presence of an abdominal wall hernia.
|
6 months post-operatively
|
|
Evaluate the quality of life in patients with abdominal wall hernias using a user-friendly survey that is designed specifically for this population of patients
Periodo de tiempo: 1 year post-operatively
|
The aim of this study is to evaluate the quality of life in patients with abdominal wall hernias using a user-friendly survey that is designed specifically for this population of patients.
We would like to use this survey to elucidate how quality of life of the patient is changed with the presence of an abdominal wall hernia.
|
1 year post-operatively
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Investigadores
- Investigador principal: Conor Delaney, MD, PhD, University Hospitals of Cleveland/ Institute for Surgical Innovation
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio
1 de octubre de 2005
Finalización primaria (Actual)
1 de abril de 2008
Finalización del estudio (Actual)
1 de mayo de 2008
Fechas de registro del estudio
Enviado por primera vez
1 de mayo de 2007
Primero enviado que cumplió con los criterios de control de calidad
1 de mayo de 2007
Publicado por primera vez (Estimar)
2 de mayo de 2007
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
15 de diciembre de 2014
Última actualización enviada que cumplió con los criterios de control de calidad
12 de diciembre de 2014
Última verificación
1 de diciembre de 2014
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Enfermedades del Sistema Digestivo
- Neoplasias
- Neoplasias por sitio
- Neoplasias Gastrointestinales
- Neoplasias del Sistema Digestivo
- Enfermedades Gastrointestinales
- Gastroenteritis
- Enfermedades del Colon
- Enfermedades intestinales
- Condiciones Patológicas, Anatómicas
- Neoplasias Intestinales
- Enfermedades Rectales
- Enfermedades inflamatorias del intestino
- Pólipos
- Pólipos intestinales
- Enfermedades diverticulares
- Colitis
- Neoplasias colorrectales
- Enfermedad de Crohn
- Pólipos colónicos
- Colitis Ulcerativa
- Diverticulitis
Otros números de identificación del estudio
- 10-05-17
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