The Effects of FODMAPs in Patients With Irritable Bowel Syndrome (Sens-IBS)
The Effects of Fermentable Oligosaccharides, Disaccharides, Monosaccharides and Polyols (FODMAPs) in Patients With Irritable Bowel Syndrome
Patients with Irritable Bowel Syndrome (IBS) often link their symptoms to foods. Interest in dietary management recently increased, including the use of a low FODMAP diet.
To investigate relation of FODMAPs and IBS, a randomized, double-blind, cross-over trial will be carried out in adult (>18) patients with IBS according to Rome IV criteria. The aim is to assess low FODMAP diet versus moderate/high FODMAP diet in IBS patients.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
The study is a randomized, double-blind, cross-over trial.
The aim is to assess the effects of low fermentable oligosaccharides, disaccharides, monosaccharides and polyols (FODMAP) diet compared to moderate/high FODMAP diet in IBS patients on gastrointestinal symptoms and psychological factors. The primary hypothesis is that the low FODMAP diet decreases gastrointestinal symptoms compared to moderate/high FODMAP diet, and that this change is accompanied with reduced psychological distress.
IBS patients (Rome IV) are challenged with FODMAPs in this randomized, double-blinded, cross-over study. The subjects will start with the low FODMAP diet or moderate/high FODMAP diet and cross over to the other intervention (both for 7 days). In between the interventions, there is a wash-out period of at least 14 days. The subjects will receive ready-made meals from the hospital kitchen (lunch and dinner) and in between snacks. The subjects are instructed to buy breakfast themselves and the subjects will receive information on which other foods to avoid, without mentioning 'FODMAPs'. The subjects will follow their usual diet (as before initiation of the study) during the wash-out period.
Primary outcomes are change in gastrointestinal symptoms, assessed by questionnaires, including IBS Severity Scoring System (IBS-SSS) (7-10 day recall and modified daily) and Gastrointestinal Symptom Rating Scale -IBS (GSRS-IBS). A 50-point reduction in IBS-SSS indicates clinical response. Bacterial fermentation (exhaled hydrogen and methane) and visceral sensitivity will be measured using the Lactulose Nutrient Challenge Test. Secondary outcomes are change in psychological factors and assessed by questionnaires, including Central Sensitization Index (CSI), Hospital Anxiety and Depression Scale (HADS), Patient Health Questionnaire (PHQ)-15 and Visceral Sensitivity Index (VSI).
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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Non-US/Non-Canadian
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Gothenburg, Non-US/Non-Canadian, Suède, 44331
- Magnus Simrén
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Adult patients with IBS according to Rome IV criteria
Exclusion Criteria:
- allergy or documented intolerance to food
- severe cardiovascular disease
- severe hepatic disease
- severe neurological disease
- severe psychiatric disease
- celiac disease
- inflammatory bowel diseases
- diabetes
- bowel dysfunction related to previous surgery
- pregnant or lactating women
- use of antibiotics within four weeks before inclusion
- strict avoidance of foods
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Soins de soutien
- Répartition: Randomisé
- Modèle interventionnel: Affectation croisée
- Masquage: Double
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: Diet 1: moderate/high FODMAP diet. Diet 2: low FODMAP diet.
The subjects will follow the moderate/high FODMAP diet as the first intervention, and the low FODMAP diet as the second intervention.
The subjects will follow both interventions for seven days.
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The subjects will obtain meal boxes prepared in the hospital kitchen with a moderately high FODMAP content (23 grams/day)
The subjects will obtain meal boxes prepared in the hospital kitchen with a low FODMAP content (<5 grams/day)
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Expérimental: Diet 1: low FODMAP diet. Diet 2: moderate/high FODMAP diet.
The subjects will follow the low FODMAP diet as the first intervention, and the moderate/high FODMAP diet as the second intervention.
The subjects will follow both interventions for seven days.
|
The subjects will obtain meal boxes prepared in the hospital kitchen with a moderately high FODMAP content (23 grams/day)
The subjects will obtain meal boxes prepared in the hospital kitchen with a low FODMAP content (<5 grams/day)
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in Irritable Bowel Syndrome-Severity Scoring System (IBS-SSS) (7-10 days recall questionnaire)
Délai: Baseline (day 0), day 7, day 21, day 28
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Irritable Bowel Syndrome-Severity Scoring System (IBS-SSS) is a validated questionnaire that incorporates typical IBS symptoms such as abdominal pain, abdominal distension and bowel dysfunction, as well as quality of life.
Subjects rated their symptoms on a visual analogue scale.
The maximum achievable score is 500 points (sum of the 5 scales).
A reduction in the total IBS-SSS score of at least 50 points is considered to indicate a clinically significant improvement in symptoms.
The scale can also be used to classify IBS symptoms severity: <75 points (no symptoms), 75-175 points (mild symptoms), 175-300 points (moderate symptoms) and >300 points (severe symptoms).
Measured after both dietary periods and at baseline of both periods.
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Baseline (day 0), day 7, day 21, day 28
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Change in Irritable Bowel Syndrome-Severity Scoring System (IBS-SSS) (modified, daily IBS-SSS)
Délai: Daily during day 7 to 14, and day 21 to 28
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Irritable Bowel Syndrome-Severity Scoring System (IBS-SSS) is a validated questionnaire that incorporates typical IBS symptoms such as abdominal pain, abdominal distension and bowel dysfunction, as well as quality of life.
Subjects rated their symptoms on a visual analogue scale.
The maximum achievable score is 500 points (sum of the 5 scales).
A reduction in the total IBS-SSS score of at least 50 points is considered to indicate a clinically significant improvement in symptoms.
The scale can also be used to classify IBS symptoms severity: <75 points (no symptoms), 75-175 points (mild symptoms), 175-300 points (moderate symptoms) and >300 points (severe symptoms).
Measured after both dietary periods and at baseline of both periods.
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Daily during day 7 to 14, and day 21 to 28
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Change in Gastrointestinal Symptom Rating Scale - Irritable Bowel Syndrome (GSRS-IBS)
Délai: Baseline (day 0), day 7, day 21, day 28
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Change in Gastrointestinal Symptom Rating Scale - Irritable Bowel Syndrome (GSRS-IBS) measures symptom severity and symptom frequency in IBS patients and is a reliable and validated questionnaire.
Thirteen questions are evaluated and rated from 1 (no discomfort at all) to 7 (very severe discomfort) on a Likert scale.
The total scores can range from 13 to 91 (sum of the domains).
The GSRS-IBS evaluates 5 domains: abdominal pain, bloating, constipation, diarrhea and satiety.
Measured after both dietary periods and at baseline of both periods.
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Baseline (day 0), day 7, day 21, day 28
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in stool consistency and frequency, measured by Bristol Stool Form (BSF)
Délai: Baseline (day 0), day 7, day 21, day 28
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Change in Bristol Stool Form, stool consistency/frequency per day after both dietary periods
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Baseline (day 0), day 7, day 21, day 28
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Change in Hospital Anxiety and Depression Scale (HADS) score
Délai: Baseline (day 0), day 7, day 21, day 28
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The Hospital Anxiety and Depression Scale (HADS) contains 7 items for depression and 7 for anxiety.
Each item is scored from 0 to 3, and therefore the total score per sub-scale can range from 0 to 21.
When subjects score >10 on 1 or 2 of the sub-scales, clinically significant psychological distress (anxiety or depression) is likely present.
Measured after both dietary periods and at baseline of both periods.
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Baseline (day 0), day 7, day 21, day 28
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Change in Patient health questionnaire-15 (PHQ-15)
Délai: Baseline (day 0), day 7, day 21, day 28
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The (PHQ-15) is a validated questionnaire that evaluates 15 somatic symptoms and can be used as a screening tool for somatization in clinical research.
The maximum score for men is 28 and 30 for women due to a question about menstrual problems.
Measured after both dietary periods and at baseline of both periods.
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Baseline (day 0), day 7, day 21, day 28
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Change in Visceral Sensitivity Index (VSI)
Délai: Baseline (day 0), day 7, day 21, day 28
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The Visceral Sensitivity Index (VSI) is a validated and reliable psychometric instrument which assesses gastrointestinal symptom-specific anxiety.
The VSI contains 15 items that are scored from 0 to 5, therefore the total score can range from 0 to 75.
Higher scores indicate more severe gastrointestinal symptom-specific anxiety.
Measured after both dietary periods and at baseline of both periods.
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Baseline (day 0), day 7, day 21, day 28
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Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Visceral Sensitivity and Bacterial Fermentation
Délai: Baseline (day 0)
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Visceral Sensitivity and Bacterial Fermentation measured by the Lactulose Nutrient Challenge Test.
To assess if visceral sensitivity and/or bacterial fermentation are predictors of clinical response to the low FODMAP diet or clinical worsening to the moderate/high FODMAP diet.
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Baseline (day 0)
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Change in microbiota content of frozen fecal samples
Délai: Baseline (day 0), day 7, day 21, day 28
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Fecal microbiota analysis using 16 S RNA technique and Dysbiosis Test.
Analyses will be done on samples from before and after both dietary periods.
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Baseline (day 0), day 7, day 21, day 28
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Change in metabolites content
Délai: Baseline (day 0), day 7, day 21, day 28
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Frozen urine/serum/fecal samples will be analyzed in the future by gas/liquid chromatography mass spectrometry (metabolomics) analysis.Analyses will be done on samples from before and after both dietary periods.
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Baseline (day 0), day 7, day 21, day 28
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Magnus Simrén, Professor, Göteborg University
Publications et liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 394-18
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