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临床试验/ACTRN12621001440819
ACTRN12621001440819已完成未知

Acceptance of increased daily dietary fibre in healthy participants: A preliminary feasibility study to inform a larger RCT to test the efficacy of barley on body composition and weight loss.

Queensland University of Technology0 个研究点目标入组 38 人开始时间: 2021年10月25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
38

研究概览

简要总结

We investigated how three weeks of increased fibre intake would affect appetite and satiety (feelings of hunger and fullness), and gastrointestinal comfort. Our results suggest that three weeks of increased fibre intake (a) does not affect appetite or satiety, and (b) increases the frequency of breaking or passing wind and increases stool consistency. Additionally, the baseline fibre consumption and the method of increased fibre increase (i.e., gradual increase or immediate increase) did not change the feelings of hunger and fullness. The results also indicated that the increase of additional fibre was perceived as being beneficial to overall wellbeing, influenced feelings of hunger and caused some minor short term gastrointestinal symptoms that disappeared after getting used to the product. The findings of this study further confirm that increasing fibre intake is a safe intervention that presents no additional risks over typical increased dietary fibre intake. Ultimately, we will use the feedback gathered from participants of this study and use it to help inform the methods for our next study which will use the same supplements and investigate its effect on weight loss and markers of health.

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 50 Years(—)
性别
All

入选标准

  • 1.Aged between 18 and 50 years of age;
  • 2.Male or female;
  • 3.Have a body mass index between 18.5-34.9 Kg.m-2.

排除标准

  • 1.Have a history or presence of a comorbid disease for which diet modifications may be contraindicated (e.g., diabetes, metabolic syndrome, polycystic ovary syndrome, hypoproteinemia).
  • 2.Have a history of eating disorders.
  • 3.Have a history of bariatric surgery.
  • 4.Currently taking, or have taken in the last 3 months, dietary supplements for thyroid, hyperlipidemia, hypoglycaemia, or weight loss supplements (e.g., ephedra, thermogenic compounds).
  • 5.Not have participated in a diet or clinical trial in the last 6 months.
  • 6.Females only: pre-menopausal, menopausal, are currently pregnant or are currently breastfeeding.
  • 7.Mental or cognitive impairment that limits ability to understand test instructions.

研究者

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