ACTRN12620000597998已完成2 期
Feasibility and acceptability of an online pre-conception weight loss program for women with overweight and obesity? A pilot randomised controlled trial
Impromy0 个研究点目标入组 50 人开始时间: 2020年5月22日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 40 Years(—)
- 性别
- Female
入选标准
- •–Women with a BMI greater than or equal to 25kg/m2;
- •–Aged >/= 18 - 40 years;
- •–Willing to attend CPA RPA clinic on 3 occasions;
- •–Willing to follow a weight loss dietary protocol for 10 weeks
- •–Has been weight stable (i.e. less than 3 kg weight loss) for the past 2 months.
排除标准
- •–Significant pre-existing, diagnosed medical condition that may prevent them from participating in the study, including but not limited to: Kidney disease or renal impairment; Gall bladder disorders or stones; Liver disease (e.g. cirrhosis); severe cardiovascular disease where rapid weight loss is contraindicated eg Cardiac arrhythmia, congenital heart disease; Malabsorptive Gastrointestinal disease (including celiac, Crohns disease);
- •–History of bariatric surgery;
- •–Severe depression;
- •–Cancer (unless benign or non-progressive skin cancer);
- •–Type 1 or type 2 diabetes.
- •–Regular use of medications prescribed by a medical practitioner that are deemed unsuitable for this trial – as determined by the appointed study physician during screening process;
- •– A food allergy/intolerance to, or not willing to consume, the foods prescribed in the protocol;
- •–A person considered by the investigator to be unwilling, unlikely or unable to comprehend or comply with the study protocol;
研究者
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