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Dietary Fibres on Gut Fermentation

2026年9月19日 更新者:Kuan-Yu Lin、University of Bath

Acute Effects of Different Dietary Fibres on Gut Fermentation: A Pilot Study

The goal of this clinical trial is to learn if adding a rapidly fermenting fibre to a meal containing a slow fermenting fibre affects gut bacterial fermentation and digestive comfort in healthy adults aged 18 to 85 years. The main questions it aims to answer are:

  • Does the addition of a fast fermenting fibre to a meal containing a slow fermenting fibre change the timing and amount of gas produced by gut bacterial fermentation?
  • Does the addition of a fast fermenting fibre as a split dose effectively reduce the digestive discomfort typically caused by consuming a high dose of fibre all at once?

Researchers will compare the effect of adding fructo-oligosaccharides (FOS) over-and-above a single dietary fibre (soluble corn fibre). They will also compare whether taking FOS either all at once versus splitting it into two smaller doses affects gut bacterial fermentation and digestive comfort.

Participants will:

  • Visit the research laboratory for 3 test days, with a 1-week break between visits.
  • Avoid certain foods and fast overnight before each test day.
  • Eat a test breakfast and lunch containing the dietary fibres in different parts of the meal.
  • Provide breath samples every 30 minutes to measure gas produced by gut bacteria.
  • Answer survey questions about their digestive comfort every 30 minutes.
  • Keep a diary of their bowel movements for 5 days during each test cycle.

Short-chain fatty acids (SCFAs) produced through dietary fibre fermentation are essential for maintaining intestinal barrier integrity and regulating systemic metabolism; however, average daily fibre intake frequently remains below recommended levels. While supplementing with highly fermentable fibres, such as fructo-oligosaccharides (FOS), effectively stimulates beneficial microbial activity in the proximal colon, their rapid breakdown often triggers acute gastrointestinal discomfort, including bloating and flatulence. Conversely, soluble corn fibre (SCF) possesses a highly branched structure that ferments slowly and reaches the distal colon, exhibiting excellent gastrointestinal tolerability but yielding a lower initial peak of SCFA production.

調査の概要

詳細な説明

This study aims to investigate the effect of rapidly fermenting FOS over-and-above slowly fermenting SCF and whether this supports a "spatio-temporal fermentation profile" spanning the entire colonic tract. By balancing fermentation speeds, this strategy holds the potential to maximise total colonic fermentation yield whilst mitigating the adverse symptoms typically associated with isolated high-dose FOS intake. Furthermore, the study explores a split-dosing regimen as an additional temporal strategy; dividing the FOS intake may limit the peak rate of gas production, preventing it from exceeding the gut's natural gas clearance mechanisms, while ensuring a sustained delivery of fermentable substrates.

To evaluate these physiological dynamics, healthy adult participants will complete a randomised, double-blind, crossover trial comprising three distinct acute testing days, separated by 7-day washout periods. Under strict dietary standardisation and overnight fasting conditions, participants will consume meals containing specific dietary fibres. The acute physiological responses will be continuously monitored via non-invasive breath hydrogen and methane analysis to objectively map fermentation kinetics, alongside regular self-reported assessments of gastrointestinal tolerability throughout the testing window.

研究の種類

介入

入学 (推定)

20

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Somerset
      • Bath、Somerset、イギリス、BA2 7AY
        • 募集
        • University of Bath
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~85年 (大人、高齢者)

健康ボランティアの受け入れ

はい

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Healthy males and females, aged between 18 and 85 years at the start of the study.
  • Self-reported regular bowel habits, defined as an average frequency of between 3 and 21 bowel movements per week (Mitsuhashi et al., 2018). This weekly average accounts for normal daily fluctuations while ensuring an overall healthy baseline.
  • Willing and able to comply with all study protocols, including pre-test dietary restrictions (avoiding highly fermentable foods), a 12-hour overnight fast, and consumption of the prescribed dietary fibre test meals.
  • Willing to accurately record gastrointestinal symptoms using the Visual Analogue Scale (VAS) and complete the Bristol Stool Scale (BSS) logs over the specified periods.
  • Able to understand the study procedures and provide written informed consent.

Exclusion Criteria:

  • History or current diagnosis of chronic gastrointestinal diseases or conditions (e.g., Irritable Bowel Syndrome [IBS], Inflammatory Bowel Disease [IBD], coeliac disease, chronic constipation, or history of major gastrointestinal surgery).
  • Use of systemic antibiotics, prebiotics, probiotics, or medications known to significantly alter gastrointestinal motility within the 3 months prior to the commencement of, or during the study period.
  • Known food allergies or severe intolerances to any ingredients present in the test meals (e.g., soluble corn fibre, fructo-oligosaccharides).
  • Females who are currently pregnant, planning to become pregnant during the study period, or lactating.
  • Currently following a highly restrictive or extreme diet (e.g., strict ketogenic, extreme high-fibre, or medically prescribed diets) that could significantly confound the baseline gut microbiota or fermentation profile.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:基礎科学
  • 割り当て:ランダム化
  • 介入モデル:クロスオーバー割り当て
  • マスキング:ダブル

武器と介入

参加者グループ / アーム
介入・治療
アクティブコンパレータ:SCF Alone

Participants will consume a standardised breakfast containing SCF in the drink component. Three hours later, they will consume a standardised low-fibre lunch.

Administration of SCF with breakfast.

実験的:Single Combined Dose (SCF + FOS)

Participants will consume a standardised breakfast containing SCF in the drink component. They will also consume a meal containing a full dose of FOS. Three hours later, they will consume a standardized low-fibre lunch.

Administration of FOS as a single dose over-and-above SCF with breakfast.

実験的:Split-Dosed Combination (SCF + FOS)

Participants will consume a standardised breakfast containing SCF in the drink component. They will also consume a meal containing half the dose of FOS. Three hours later, they will consume a standardized low-fibre lunch containing the other half of the dose of FOS.

Administration of FOS at breakfast and at lunch, over-and-above SCF at breakfast.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Area Under the Curve (AUC) of Breath Hydrogen and Methane Production
時間枠:Baseline (fasting) and every 30 minutes up to 8 hours on each acute test day

Total colonic fermentation yield is evaluated by measuring breath hydrogen and methane concentrations. Breath samples are collected at 30-minute intervals post-intervention using Omed breath analysers. The total production for both gases is quantified independently by calculating their respective AUC values from the averaged concentration-time profiles.

Baseline (fasting) and every 30 minutes up to 8 hours on each acute test day

二次結果の測定

結果測定
メジャーの説明
時間枠
Fermentation Kinetic Parameters: Maximum Peak Concentration (Cmax) of Breath Gases
時間枠:Baseline (fasting) and every 30 minutes up to 8 hours on each acute test day.

The dynamic temporal characteristics of gut fermentation are evaluated by determining the maximum peak concentration (Cmax) for both breath hydrogen and methane. Data is extracted from continuous breath samples collected using Omed breath analysers.

Baseline (fasting) and every 30 minutes up to 8 hours on each acute test day.
Fermentation Kinetic Parameters: Time to Peak (Tmax) of Breath Gases
時間枠:Baseline (fasting) and every 30 minutes up to 8 hours on each acute test day.

The dynamic temporal characteristics of gut fermentation are evaluated by determining the time required to reach this peak concentration (Tmax) for both breath hydrogen and methane. Data is extracted from continuous breath samples collected using Omed breath analysers.

Baseline (fasting) and every 30 minutes up to 8 hours on each acute test day.
Acute Gastrointestinal (GI) Tolerability Composite Score
時間枠:Baseline (fasting) and every 30 minutes up to 8 hours on each acute test day.

The incidence and severity of subjective GI symptoms (bloating, abdominal cramping, stomach noises/borborygmi, and flatulence) are rated by participants on a scale from 0 (absent) to 10 (extremely severe). Any bowel movements are logged and converted into a stool score from 0 (normal transit) to 10 (diarrhoea). These are summed to calculate a total composite score ranging from 0 to 50, with higher scores indicating worse GI tolerability.

Baseline (fasting) and every 30 minutes up to 8 hours on each acute test day.
Lower Gastrointestinal Response Assessed by the Bristol Stool Scale (BSS)
時間枠:Baseline (fasting) and every 30 minutes up to 8 hours on each acute test day.

Participants monitor and log their daily bowel movement frequency and utilise the Bristol Stool Scale (BSS) to objectively assess stool consistency and appearance. This tracks delayed lower gastrointestinal responses beyond the immediate acute testing window.

Baseline (fasting) and every 30 minutes up to 8 hours on each acute test day.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Dylan Thompson, Dr.、University of Bath
  • 主任研究者:Oly Perkin, Dr.、University of Bath

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年8月26日

一次修了 (推定)

2027年8月27日

研究の完了 (推定)

2027年8月27日

試験登録日

最初に提出

2026年9月15日

QC基準を満たした最初の提出物

2026年9月19日

最初の投稿 (実際)

2026年9月23日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月23日

QC基準を満たした最後の更新が送信されました

2026年9月19日

最終確認日

2026年9月1日

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