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临床试验/NCT03518515
NCT03518515已完成不适用

Potato Consumption and Energy Balance: a Randomized, Controlled, Clinical Trial

University of Alabama at Birmingham2 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2018年8月2日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
180
试验地点
2
主要终点
Change in fat mass

研究概览

简要总结

A randomized, clinical trial will be performed to assess changes in body weight and fat mass with daily potato consumption versus a calorie-matched snack of almonds.

详细描述

This is a 30-day randomized, controlled trial with 3 arms: 1) non-potato food (almonds), 2) standard white potato French fry, 3) standard white potato French fry with potential glycemia-modulating spice/seasoning mix added.

Free-living study participants will be assigned to consume one of the 3 foods (calorie matched) each day for a 30-day period. Body composition (via dual energy x-ray absorptiometry; DXA), and blood chemistry will be assayed at baseline and study completion, along with a sub-sample of subjects participating in a meal-based tolerance tests at study completion.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 18- 50 years old
  • Body mass index (BMI) 20- 35
  • No dietary restrictions or allergies
  • Weight stable
  • Access to camera through smartphone, computer or tablet

排除标准

  • Pregnancy or anticipating pregnancy or lactation
  • Nut or food allergy
  • Diagnosed diabetes (Type 1 or 2)
  • History of weight control surgery (bariatric or liposuction)
  • Consumes >1 serving of potatoes daily before enrollment
  • Weight loss or gain >5% within past 6 months
  • Medical conditions or medications that would prevent the ability to comply with treatment assignment and/or affect energy balance
  • Dependence on others for food procurement or preparation

结局指标

主要结局

Change in fat mass

时间窗: baseline and study completion (30 days)

Determined by dual-energy X-ray absorptiometry.

次要结局

  • Change in fasting insulin(baseline and study completion (30 day))
  • Change in fasting glucose(baseline and study completion (30 day))
  • Change in body weight(baseline and study completion (30 day))
  • Change in HbA1c(baseline and study completion (30 day))
  • Change in caloric Intake(baseline and study completion (30 days))
  • Meal Tolerance Test(Study Completion (30 day))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Daniel L. Smith, Jr.

Co-Principal Investigator

University of Alabama at Birmingham

研究点 (2)

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