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Effects of Journaling on Weight Loss

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

Tracking

+ Journaling

+ Website

Conductual
Quiénes están siendo reclutados

Peso Corporal+5

+ Cambios en el Peso Corporal

+ Trastornos de la Nutrición

De 21 a 65 años
+17 Criterios de eligibilidad
Ver todos los criterios de elegibilidad
Cómo está diseñado el estudio

Estudio de Tratamiento

Intervencional
Inicio del estudio: agosto de 2012
Ver detalles del protocolo

Resumen

Patrocinador PrincipalMilton S. Hershey Medical Center
Última actualización: 4 de febrero de 2013
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Fecha de inicio: 1 de agosto de 2012

Fecha en la que se inscribió al primer participante.

Participants will call study line given on recruitment materials and be screened over the phone. Baseline visit: Individuals who meet the screening criteria will be invited to a one-hour training session about the website and diet plan book. During the training, a coordinator will review the consent form with the participants and ask if they have any questions. The coordinator will take consented individuals' height, weight and blood pressure measurements. Participants will be given a pedometer to use during physical activities and a meal replacement book to use as a resource. After baseline visit: All participants will complete surveys online (Demographics, Three-Factor Eating Questionnaire, Motivation, Weight Loss Habits, Medication log, International Physical Activity Questionnaire) and be randomized into one of two groups. The intervention group will be asked to record their weight, physical activity steps, pre-portioned food items and journal entries on a daily basis. The control group will be sent an email informing them they will have access to the tracking, journals and website in three months. Intervention Group: Participants will receive daily emails with links to record their weight, physical activity steps and pre-portioned food items; participants will also complete a journaling response to two writing prompts. The emails will contain links to the website to be used as a resource. Every week, participants will enter whether they have an appointment with primary care provider in the next week. Participants will also receive weekly blogs from the principal investigator; participants can opt out of receiving the blog emails at any time. Coordinators will review the database weekly. If a participant has lost ten pounds, they will be emailed to call their doctor since weight loss can affect blood pressure and medication needs. If a participant has an upcoming primary care provider appointment, they will be emailed to print out their tracking graphs (weight, steps taken, meal replacements). Coordinators will also monitor journal responses; coordinators will contact participants who wrote useful entries to ask if the participant's responses can be shared with other participants. Shared posts will be anonymous; only the age of the individual will be given. Month one and two visits: Participants from both groups will be asked to come to Hershey Medical Center to have their height, weight and blood pressure measured. Month three visit: Participants from both groups will be asked to come to Hershey Medical Center to have their height, weight and blood pressure measured. Prior to their visit, participants will be asked to complete a series of surveys online (Three-Factor Eating Questionnaire, Motivation, Weight Loss Habits, Medication log, International Physical Activity Questionnaire, Satisfaction). Participants in the control group will be given a booklet containing the writing prompts, tracking and website address to complete on their own if they so choose. Participants will be asked if they would like to come back for an optional video interview. The interview will consist of six questions about their experience with the study.

Patrocinador PrincipalMilton S. Hershey Medical Center
Última actualización: 4 de febrero de 2013
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 100 pacientes

Número total de participantes que el ensayo clínico espera reclutar.

Estudio de Tratamiento

Estos estudios prueban nuevas formas de tratar una enfermedad, condición o problema de salud. El objetivo es determinar si un nuevo medicamento, terapia o enfoque funciona mejor o tiene menos efectos secundarios que las opciones existentes.



Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios

Cualquier sexo

Sexo biológico de los participantes elegibles para inscribirse.

De 21 a 65 años

Rango de edades de los participantes que pueden unirse al estudio.

Voluntarios sanos no permitidos

Indica si personas sanas, sin la condición que se estudia, pueden participar.

Condiciones

Patología

Peso CorporalCambios en el Peso CorporalTrastornos de la NutriciónEnfermedades Nutricionales y MetabólicasSignos y SíntomasCondiciones Patológicas, Signos y SíntomasObesidadPérdida de peso

Criterios

4 criterios de inclusión requeridos para participar
21 to 65 years old

Able to read, write, and understand English

Body mass index between 27 and 45

E-mail and Internet access

13 criterios de exclusión impiden participar
Been told by doctor of heart trouble

Bone or joint problem that has been or might be aggravated by exercise

Current use of weight loss medication or program

Frequent pains in heart and chest

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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

Experimental
In addition to standard care, participants will complete daily tracking and journaling and receive weekly feedback based on their individual entries.

Grupo II

Comparador Activo
Participants receive standard care

Objetivos del Estudio

Objetivos Primarios

Objetivos Secundarios

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

Penn State Milton S. Hershey Medical Center

Hershey, United StatesAbrir Penn State Milton S. Hershey Medical Center en Google Maps
Completado1 Centros de Estudio