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.
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.
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