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临床试验/NCT02966431
NCT02966431终止不适用

Effects of a Weight Loss Intervention in College-age Women

Texas Christian University1 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2017年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
4
试验地点
1
主要终点
Body weight

研究概览

简要总结

Determine the effects of an 8-week weight loss intervention.

详细描述

The purpose of this study is three-fold: 1) Determine whether an 8-week, patient-centered, weight loss intervention can be successfully implemented in overweight, college-age females for promotion of weight loss and prevention of weight regain at 8-weeks, three months, and six months follow-up; 2) Determine the effects of the intervention on established markers of calorie restriction, energy expenditure and body composition; 3) Determine the effects of a liquid meal on physiological and subjective markers of hunger and satiety from pre- to post- 8wk intervention in the intervention group vs control group.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 25 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Females age 18-25years
  • •Body Mass Index 25.0 to 29.9 kg/m2 (overweight)
  • •Agree to receive frequent contacts from investigators and communicate with program staff for up to 6 months
  • •Willing to measure blood glucose via finger prick test three to eight times per day for two weeks
  • •Able to give written informed consent
  • •Able to comply with study procedures

排除标准

  • •Unable or unwilling to give informed consent
  • •Travel plans that do not permit participation
  • •Pregnant or planning on becoming pregnant during the 6 months of participation in the study
  • •Weight loss or gain exceeding 5% of body weight in the past 3 months
  • •Current participation in a weight loss program
  • •Diagnosis of mental disorder or chronic disease
  • •History of eating disorder such as anorexia nervosa, bulimia nervosa, or binge eating disorder (unless approved by program staff)
  • •History of surgery or procedure that could affect swallowing or digestion
  • •Any person who is on a medically prescribed diet
  • •Any current supplement use other than a daily multivitamin
  • •Any current metabolic medication use other than birth control
  • •Any bleeding disorders or blood clotting problems
  • •Anyone who has donated blood or plasma in the last 20 days
  • •Any tobacco or illicit drug users
  • •Anyone who has allergies to any of the components of the liquid meal

研究组 & 干预措施

Counseling

Experimental

Receive counseling for 8-wks

干预措施: Counseling (Behavioral)

Control

Placebo Comparator

Does not receive counseling for 8-wks

干预措施: No Counseling (Behavioral)

结局指标

主要结局

Body weight

时间窗: 18 months

次要结局

未报告次要终点

研究者

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

Jada Stevenson

Assistant Professor

Texas Christian University

研究点 (1)

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