- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT03355729
The Quebec Family Study (QFS): Role of Genetic Factors in Obesity and Its Related Risk Factors and Diseases (QFS)
27 de noviembre de 2017 actualizado por: Louis Pérusse
The Quebec Family Study: an Observational Study Aimed at Investigating the Role of Genetic Factors in Physical Fitness, Obesity and Risk Factors for Common Diseases and Health-related Behaviours
The Quebec Family Study (QFS) is an observational study that was planned to investigate the role of genetic factors in physical fitness, body composition, risk factors for common disease and health-related behaviour.
Descripción general del estudio
Estado
Terminado
Condiciones
Descripción detallada
The Quebec Family Study was an observational study with three cycles of data collection between 1978 and 1992.
During the first cycle of data collection (Phase 1: 1978-1982), a total of 1,650 subjects from 375 families were recruited.
During the second cycle (Phase 2: 1989-1997), 385 subjects from 105 phase 1 families were retested and an additional 372 subject from 74 families were recruited.
During the third cycle (Phase 3: 1998-2002), 204 subjects from phase 1 were tested a third time, 113 subjects from phase 2 were tested a second time and 194 new subjects from 44 families were recruited.
Tipo de estudio
De observación
Inscripción (Actual)
951
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
10 años y mayores (Niño, Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
N/A
Géneros elegibles para el estudio
Todos
Método de muestreo
Muestra no probabilística
Población de estudio
The QFS cohort is a mixture of random sampling and ascertainment through obese individuals.
In Phase 1 of the study, subjects were randomly selected from French-Canadian families living in the Quebec city area, In Phases 2 and 3 of the study, families with a least one obese parent and one obese offspring were recruited.
Descripción
Inclusion Criteria:
- Age over 10 years
Exclusion Criteria:
- Not applicable
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 |
---|---|---|
Body composition
Periodo de tiempo: Through study completion, an average of 24 years
|
Body composition as assessed by underwater weighing
|
Through study completion, an average of 24 years
|
Body mass index (kg/m^2)
Periodo de tiempo: Through study completion, an average of 24 years
|
Body mass index assessed from height and weight
|
Through study completion, an average of 24 years
|
Abdominal fat
Periodo de tiempo: Through study completion, an average of 24 years
|
Abdominal fat as assessed by commuted tomography
|
Through study completion, an average of 24 years
|
Waist and hip circumferences (cm)
Periodo de tiempo: Through study completion, an average of 24 years
|
Waist and hip circumferences (cm)
|
Through study completion, an average of 24 years
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Caloric intake
Periodo de tiempo: Through study completion, an average of 24 years
|
Total caloric intake and macronutrient intake using a 3-day dietary record
|
Through study completion, an average of 24 years
|
Eating behaviour
Periodo de tiempo: Through study completion, an average of 24 years
|
Eating behaviour assessed using the Three-Factor Eating questionnaire
|
Through study completion, an average of 24 years
|
Energy expenditure
Periodo de tiempo: Through study completion, an average of 24 years
|
Oxygen consumption at rest and during exercise
|
Through study completion, an average of 24 years
|
Physical activity level
Periodo de tiempo: Through study completion, an average of 24 years
|
Physical activity level assessed by questionnaire
|
Through study completion, an average of 24 years
|
Blood pressure (mm Hg)
Periodo de tiempo: Through study completion, an average of 24 years
|
Systolic and diastolic blood pressure
|
Through study completion, an average of 24 years
|
Plasma lipid levels (mmol/L)
Periodo de tiempo: Through study completion, an average of 24 years
|
Fasting levels of triglycerides, LDL-cholesterol and HDL-cholesterol in mmo/L
|
Through study completion, an average of 24 years
|
Glucose levels (mmol/L)
Periodo de tiempo: Through study completion, an average of 24 years
|
Plasma glucose levels in a fasting state and following an oral glucose tolerance test, inflammatory markers. Plasma glucose levels in a fasting state and during an oral glucose tolerance test |
Through study completion, an average of 24 years
|
Insulin levels (pmol/L)
Periodo de tiempo: Through study completion, an average of 24 years
|
Plasma insulin levels in a fasting state and following an oral glucose tolerance test.
|
Through study completion, an average of 24 years
|
C-reactive protein (CRP in mg/ml)
Periodo de tiempo: Through study completion, an average of 24 years
|
C-reactive protein (CRP in mg/ml)
|
Through study completion, an average of 24 years
|
Adiponectin levels (in micrograms/ml)
Periodo de tiempo: Through study completion, an average of 24 years
|
Adiponectin levels (in micrograms/ml)
|
Through study completion, an average of 24 years
|
Interleukin-6 (IL6) and tumor necrosis factor-alpha (TNF-alpha) in pg/ml
Periodo de tiempo: Through study completion, an average of 24 years
|
Interleukin-6 (IL6) and tumor necrosis factor-alpha (TNF-alpha) in pg/ml
|
Through study completion, an average of 24 years
|
Smoking habits (nb of cigarettes per day)
Periodo de tiempo: Through study completion, an average of 24 years
|
Smoking habits (nb of cigarettes per day)
|
Through study completion, an average of 24 years
|
Sleeping (hours/day)
Periodo de tiempo: Through study completion, an average of 24 years
|
Sleeping (hours/day)
|
Through study completion, an average of 24 years
|
Alcohol consumption
Periodo de tiempo: Through study completion, an average of 24 years
|
Alcohol consumption (nb of drinks per week)
|
Through study completion, an average of 24 years
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Claude Bouchard, Ph.D., Pennington Biomedical Center
- Director de estudio: Louis Perusse, Ph.D., Laval University
Publicaciones y enlaces útiles
La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.
Publicaciones Generales
- Chaput JP, Perusse L, Despres JP, Tremblay A, Bouchard C. Findings from the Quebec Family Study on the Etiology of Obesity: Genetics and Environmental Highlights. Curr Obes Rep. 2014 Jan 4;3(1):54-66. doi: 10.1007/s13679-013-0086-3. eCollection 2014.
- Jacob R, Drapeau V, Tremblay A, Provencher V, Bouchard C, Perusse L. The role of eating behavior traits in mediating genetic susceptibility to obesity. Am J Clin Nutr. 2018 Sep 1;108(3):445-452. doi: 10.1093/ajcn/nqy130.
Enlaces Útiles
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 (Actual)
1 de junio de 1978
Finalización primaria (Actual)
5 de septiembre de 2002
Finalización del estudio (Actual)
5 de septiembre de 2002
Fechas de registro del estudio
Enviado por primera vez
16 de noviembre de 2017
Primero enviado que cumplió con los criterios de control de calidad
27 de noviembre de 2017
Publicado por primera vez (Actual)
28 de noviembre de 2017
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
28 de noviembre de 2017
Última actualización enviada que cumplió con los criterios de control de calidad
27 de noviembre de 2017
Última verificación
1 de noviembre de 2017
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 2010-075 CG
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
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. .