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Portion Size Strategies for Management of Body Weight

14 de mayo de 2015 actualizado por: Barbara J. Rolls, Penn State University

The primary aim of this research is to determine the efficacy of two portion-control strategies to achieve sustainable dietary and behavior changes and to promote weight loss and maintenance. A randomized controlled trial will test two approaches to managing portion sizes: one that gives individuals skills and tools to help them make appropriate portion choices, and another that focuses on consumption of pre-portioned foods in order to limit exposure to large portions in the personal food environment. A third group will receive a basic nutritional program to promote weight loss.

The second aim of the research is to determine the effects of the programs on knowledge and consumption of appropriate portions, as assessed by innovative assessment methods and multiple-pass dietary recalls. The third aim is to conduct exploratory analyses of individual factors that may influence the response to the portion-control interventions, such as psychosocial indicators, blood biomarkers, and measures of adherence to the interventions. The expected outcome of the project is that it will lead to the development of specific, evidence-based strategies to help control portion sizes in order to manage weight.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Actual)

186

Fase

  • No aplica

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

    • Pennsylvania
      • University Park, Pennsylvania, Estados Unidos, 16803
        • Penn State University Laboratory for the Study of Human Ingestive Behavior

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

20 años a 65 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Femenino

Descripción

Inclusion Criteria:

  • Body mass index of 28 to 45 kg/m squared
  • Able to safely engage in physical activity (walking)
  • Able to attend regular instructional sessions at University Park, Pennsylvania

Exclusion Criteria:

  • have a medical condition diagnosed by a physician that precludes participation
  • report symptoms indicative of depression or disordered eating
  • report serious food allergies or intolerance
  • current or planned participation in a weight-loss program
  • pregnant or lactating or planning to become pregnant in the next 18 months

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

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Portion size instruction
Advice on diet, physical activity, and behavior change. Instruction in food portion size.
Individuals will participate in individual sessions with Registered Dietitians providing basic instruction in principles of weight loss. The program will instruct individuals on the principles of healthy eating and nutrition during calorie restriction. These materials include one module with general information on the importance of limiting portion sizes. The program will also include instruction on physical activity and behavioral strategies for weight loss.
Individuals assigned to this program will participate in individual instructional sessions with specialized materials and tools that address food selection and choosing appropriate portion sizes of various foods.
Experimental: Pre-portioned foods
Advice on diet, physical activity, and behavior change. Provision of pre-portioned foods.
Individuals will participate in individual sessions with Registered Dietitians providing basic instruction in principles of weight loss. The program will instruct individuals on the principles of healthy eating and nutrition during calorie restriction. These materials include one module with general information on the importance of limiting portion sizes. The program will also include instruction on physical activity and behavioral strategies for weight loss.
Individuals assigned to this program will be provided with commercially available pre-portioned foods and will be taught effective ways to incorporate them into their daily diet.
Comparador activo: Comparison
Advice on diet, physical activity, and behavior change. Advice on healthy eating for weight loss.
Individuals will participate in individual sessions with Registered Dietitians providing basic instruction in principles of weight loss. The program will instruct individuals on the principles of healthy eating and nutrition during calorie restriction. These materials include one module with general information on the importance of limiting portion sizes. The program will also include instruction on physical activity and behavioral strategies for weight loss.
Individuals assigned to this program will participate in individual instructional sessions that address principles of healthy eating while on a calorie-restricted diet.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in body weight
Periodo de tiempo: Months 0 to 12
Body weight will be measured at multiple time points during the 12-month trial; the main outcome will be the weight trajectory across this time
Months 0 to 12

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in portion size selection, perception, and knowledge
Periodo de tiempo: Months 0, 3, 6, & 12
Computerized assessment of various foods (for self-selected portion sizes, estimation of calorie content, and satiety value) and general knowledge about portion size
Months 0, 3, 6, & 12
Change in portion size consumption
Periodo de tiempo: Months 0, 3, 6, & 12
Portion sizes consumed in various food categories as assessed by diet recalls and diet records
Months 0, 3, 6, & 12
Change in blood biomarkers
Periodo de tiempo: Months 0, 3, 6, & 12
Fasting lipids, glucose, insulin, and calculated insulin resistance
Months 0, 3, 6, & 12
Change in waist circumference
Periodo de tiempo: Months 0, 3, 6, & 12
Months 0, 3, 6, & 12
Change in blood pressure
Periodo de tiempo: Months 0, 3, 6, & 12
Months 0, 3, 6, & 12
Change in dietary intakes
Periodo de tiempo: Months 0, 3, 6, 9, & 12
Energy intake, nutrient intakes, dietary energy density, food group intakes, and diet quality from three days of 24-hour diet recalls
Months 0, 3, 6, 9, & 12
Change in step counts
Periodo de tiempo: Months 0, 3, 6, 9, & 12
Daily step counts from pedometers
Months 0, 3, 6, 9, & 12
Change in attitudes and behaviors related to food and eating
Periodo de tiempo: Months 0, 1, 3, 6, & 12
Self-reported eating attitudes and behaviors on multiple questionnaires
Months 0, 1, 3, 6, & 12
Change in psychosocial characteristics
Periodo de tiempo: Months 0, 3, 6, & 12
Questionnaires measuring psychosocial characteristics including impulsivity, variety-seeking, and self-efficacy
Months 0, 3, 6, & 12
Intervention adherence
Periodo de tiempo: Month 12
Number of sessions attended, number of diet and activity records completed, and frequency of using intervention strategies during the entire trial
Month 12

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Barbara J. Rolls, PhD, Penn State 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.

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 julio de 2012

Finalización primaria (Actual)

1 de marzo de 2015

Finalización del estudio (Actual)

1 de marzo de 2015

Fechas de registro del estudio

Enviado por primera vez

15 de noviembre de 2011

Primero enviado que cumplió con los criterios de control de calidad

17 de noviembre de 2011

Publicado por primera vez (Estimar)

18 de noviembre de 2011

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

15 de mayo de 2015

Última actualización enviada que cumplió con los criterios de control de calidad

14 de mayo de 2015

Última verificación

1 de mayo de 2015

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • PortionSize101
  • R01DK059853 (Subvención/contrato del NIH 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. .

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