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临床试验/ACTRN12620000920998
ACTRN12620000920998已完成未知

Comparing the effects of 12 weeks of resistance training combined with 5:2 intermittent fasting or continuous energy restriction on body composition, strength, compliance, metabolic health and gut microbiome in normal weight, overweight and obese adults.

Swinburne University of Technology0 个研究点目标入组 44 人开始时间: 2020年9月17日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
44

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
Open (masking not used)

入排标准

年龄范围
18 Years 至 45 Years(—)
性别
All

入选标准

  • 1. Aged between 18-45 years
  • 2. BMI of 22.0-35.0
  • 3. Body fat percentage >18% for males and >25% for females as assessed by dual x-ray absorptiometry
  • 4. No structured resistance training program in the previous 6 months
  • 5. Weight stable for 3 months prior to the study (<5% weight loss or weight gain)

排除标准

  • 1. Smokers
  • 2. Have diabetes
  • 3. Have a history of cardiovascular disease
  • 4. Are taking dietary supplements and unwilling to cease for the duration of the study
  • 5. Taking glucose, blood lipid lowering or weight loss medication.
  • 6. Have a current physical condition that could be exacerbated by resistance training (as determined by GP).
  • 7. Are pregnant/intend to become pregnant during the course of the study
  • 8. Are menopausal/post-menopausal
  • 9. Have a history of disordered eating
  • 10. Have a current or previous respiratory condition likely to be exacerbated by the intervention
  • 11. Have a current or previous gastrointestinal disorder likely to be exacerbated by the intervention
  • 12. Have an allergy to any components of the provided supplement
  • 13. Were unable to commit to fasting if in the 5:2 intermittent fasting group
  • 14. Do not speak English at a level with which they are able to understand and complete the requirements of the study or
  • 14. Any other disclosed chronic disease or condition, or taking any other medication that investigators deem would contraindicate the study intervention.

研究者

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