Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
20 participants
INTERVENTIONAL
2024-10-01
2025-10-01
Brief Summary
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Detailed Description
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It is known that HPDs provide more effective results in body weight loss compared to low protein diets. It is suggested that this effect occurs as a result of increased thermogenesis, increased satiety and suppressed appetite, and reduced glycemic index and glycemic load due to the replacement of refined carbohydrates with proteins. In addition to this positive effect on weight loss, there are possible short- and long-term side effects of HPD nutrition. Known complications of long-term HPD nutrition include increased cardiovascular disease risk, blood pressure, blood lipids, and kidney dysfunction. Cardiovascular problems in particular are a source of concern because they will counteract the short-term positive effect of HPD on weight loss and increase the burden of cardiovascular disease in the long term. Studies generally focus on HPD and weight loss; there is limited data on the relationship between HPD nutrition and metabolic dysfunction such as endothelial dysfunction, inflammatory markers, antioxidant status, and other chronic diseases. The physiological, biochemical, and molecular events that occur due to high protein diet nutrition have not been fully understood and their results have not been explained.
High protein diets (especially low carbohydrate diets) are thought to have negative effects because they cause a decrease in fruit and vegetable consumption. In those who eat a HPD, especially inadequate vitamin A, C and E in their diets, this will have a negative effect on antioxidant systems and will pave the way for the development of many chronic and metabolic diseases in the long term. Despite the positive effects of HPD applied as a weight loss diet in the short term, it is thought that the oxidative stress and inflammation it will create in the long term will cause an increase in chronic and metabolic diseases as well as comorbidities. This increase in the disease burden will increase health expenditures both individually and socially.
Therefore, this study was planned to provide information about the effect of short-term HPD feeding on early antioxidant response in adult, healthy, normal body mass index female individuals. As a result of the study, it is thought that short-term HPD feeding will cause an increase in oxidative stress, a decrease in antioxidant capacity and an increase in inflammatory biomarkers.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
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High Protein Diet
The energy composition of the high protein diet will be calculated as 40% carbohydrate, 30% protein and 30% fat. It will be stated that individuals should not eat anything other than the foods to be sent during the weeks of the diet.
High Protein Diet
Individuals will be placed on a high protein diet for 10 days.
Normal Protein Diet
The energy composition of the high protein diet will be calculated as 55% carbohydrate, 15% protein and 30% fat. It will be stated that individuals should not eat anything other than the foods to be sent during the weeks of the diet.
Normal Protein Diet
Individuals will be placed on a normal protein diet for 10 days.
Interventions
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High Protein Diet
Individuals will be placed on a high protein diet for 10 days.
Normal Protein Diet
Individuals will be placed on a normal protein diet for 10 days.
Eligibility Criteria
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Inclusion Criteria
* Not changing physical activity throughout the study,
* Having a BMI of 18.5-24.9 kg/m2,
* Being healthy
Exclusion Criteria
* Having a chronic disease,
* Smoking and drinking alcohol,
* Using vitamin-mineral supplements and herbal supplements,
* Being pregnant or breastfeeding,
* Having entered menopause,
* Being on any diet.
19 Years
45 Years
ALL
Yes
Sponsors
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TC Erciyes University
OTHER
Responsible Party
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Aslı Onur Canaydın
Research Assistant
Central Contacts
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Other Identifiers
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ERU-BES-AOC-02
Identifier Type: -
Identifier Source: org_study_id
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