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Supplements for Controlling Resistance to Insulin

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StatusRescindido
Patrocinadores
University of Southern California
Colaboradores
InterHealth Nutraceuticals, Inc.

Palavras-chave

Resumo

The purpose of this study is to evaluate the effects of a combination of hydroxcycitrate (HCA) and niacin-bound chromium, in conjunction with nutrition education, over a twelve week period. Participants will be evaluated with regard to BMI, percent body fat, insulin activity, and hunger.

Descrição

The prevalence of obesity among youth has increased dramatically in recent years. Parallel to the increased rates of pediatric obesity, overweight children present clinically with adiposity related comorbidities such as insulin resistance and type 2 diabetes. The prevailing recommendations for overweight youth are to increase physical activity levels and limit energy intake in order to improve body composition. Currently there is little empirical evidence to support the efficacy of these recommendations. Alternatively, evidence in adults suggests that nutritional supplementation with (-) hydroxycitric acid (HCA), an organic acid found naturally in citrus fruits, and chromium may lead to favorable changes in body composition and improve glucose regulation. To date, these issues have not been tested in youth. Therefore, the purpose of the present investigation is to examine the effects of a nutritional education program combined with either HCA + chromium or placebo on measures of body composition and glucose regulation in overweight adolescents.

datas

Última verificação: 04/30/2019
Enviado pela primeira vez: 06/15/2008
Inscrição estimada enviada: 06/16/2008
Postado pela primeira vez: 06/17/2008
Última atualização enviada: 05/30/2019
Última atualização postada: 06/24/2019
Data dos primeiros resultados enviados: 09/22/2011
Data dos primeiros resultados de QC enviados: 03/28/2017
Data dos primeiros resultados postados: 05/10/2017
Data real de início do estudo: 01/31/2008
Data Estimada de Conclusão Primária: 07/31/2008
Data Estimada de Conclusão do Estudo: 07/31/2008

Condição ou doença

Obesity
Diabetes Mellitus, Type 2

Intervenção / tratamento

Drug: 1 - nutrition education plus active supplement

Drug: 2 - nutrition education plus inactive supplement

Fase

Fase 4

Grupos de Armas

BraçoIntervenção / tratamento
Active Comparator: 1 - nutrition education plus active supplement
nutrition education plus active supplement
Drug: 1 - nutrition education plus active supplement
After all baseline measures have been completed, participants will be randomly assigned to either the nutrition education + supplement group, or the nutrition education + placebo group. The length of the intervention is twelve weeks. Nutrition classes will take place once a week for 1 1/2 hours. Subjects will be encouraged to increase fiber and decrease sugar intake. They will also be separated into gender-specific classes. Active and inactive supplements will be identical in appearance and taste. Active supplements will contain 2,700 mgs/day of Super CitriMax (hydroxycitrate)and 400 µg per day of ChromeMate (niacin-bound Chromium). Supplements will be in powder and tablet form, and should be taken 30 minutes prior to each meal.
Placebo Comparator: 2 - nutrition education plus inactive supplement
nutrition education plus inactive supplement
Drug: 2 - nutrition education plus inactive supplement
After all baseline measures have been completed, participants will be randomly assigned to either the nutrition education + supplement group, or the nutrition education + placebo group. The length of the intervention is twelve weeks. Nutrition classes will take place once a week for 1 1/2 hours. Subjects will be encouraged to increase fiber and decrease sugar intake. They will also be separated into gender-specific classes. Active and inactive supplements will be identical in appearance and taste.

Critério de eleição

Idades qualificadas para estudar 13 Years Para 13 Years
Sexos elegíveis para estudoAll
Aceita Voluntários Saudáveissim
Critério

Inclusion Criteria:

- Age

- All subjects will be between 13 and 17 years of age

- Overweight

- All subjects will be overweight as defined by an age & sex-specific body mass index ≥ 85th percentile based on CDC BMI growth charts [US Department of Health and Human Services, 2000], calculated by Epi Info Software, version 3.3.

Exclusion Criteria:

- Presently taking any prescribed medication(s) or diagnosed with any syndrome or disease that could influence dietary intake, body composition and fat distribution, or insulin action or secretion.

- Previously diagnosed with any major illness since birth (e.g. sever intrauterine growth retardation, chronic birth asphyxia, cancer).

- Children with type 1 and/or type 2 diabetes will be excluded are referred to a physician.

- Currently involved with any dietary, exercise, or weight loss program or have been in the 6 months prior to participation.

- Unexplained weight loss or gain in the prior six months.

- Oral contraception use in sexually active females

- Children who live further than 20 miles away from the USC Health Science Campus (HSC).

Resultado

Medidas de Resultado Primário

1. Body Mass Index [measured at baseline and 12 weeks]

Change in Body Mass Index measurement at baseline and 12 weeks

Medidas de Resultado Secundário

1. Insulin Activity [Measured at baseline and 12 weeks]

Change in insulin activity measured at baseline and 12 weeks

2. Percent Body Fat [Measured at baseline and 12 weeks]

Change in percent body fat measured at baseline and 12 weeks

3. Hunger [Measured at baseline and 12 weeks]

Change in hunger score measured at baseline and 12 weeks

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