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临床试验/ACTRN12620000597998
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

发起方
Impromy

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