The Effects of 24-hour Fasting or Carbohydrate Restriction on Postprandial Metabolic Responses
NCT ID: NCT07250191
Last Updated: 2025-11-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
16 participants
INTERVENTIONAL
2023-10-16
2025-11-06
Brief Summary
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This study will examine how 24 hours of either complete fasting or low carbohydrate intake without energy restriction influence postprandial blood glucose and lipid concentrations, as well as related metabolic markers, in healthy adults, in comparison to a habitual high carbohydrate control diet. Participants will complete all three conditions in a randomised order, consuming a standardised meal test after each 24-hour condition. Repeated blood sampling and gas exchange measurements will be carried out to assess postprandial metabolic responses.
The aim of this study is to characterise whether acute periods of fasting and low carbohydrate restriction elicit distinct or comparable alterations in postprandial metabolic responses. A clearer understanding of these acute physiological effects can help inform how variations in eating patterns influence glucose and lipid handling in individuals without metabolic disease.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
NONE
Study Groups
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Habital control diet
100% of energy requirements, ≥150 carbohydrate/day
No interventions assigned to this group
Fasting
No energy intake
Fasting
No food intake for 24 hours
Carbohydrate Restriction
100% of energy requirements, ≤20g carbohydrate
Carbohydrate restriction
Restriction of dietary carbohydrate to ≤5% of total energy intake for 24 hours
Interventions
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Fasting
No food intake for 24 hours
Carbohydrate restriction
Restriction of dietary carbohydrate to ≤5% of total energy intake for 24 hours
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Have a BMI of 18.5-29.9 kg/m2
Exclusion Criteria
2. Use of medication that may interfere with study outcomes (e.g. glucose or lipid-lowering medications)
3. Currently or recently pregnant (within last 6 months), planning to get pregnant or currently lactating
4. Has a habitually low carbohydrate intake (\<150g carbohydrates/day)
5. Current or previous eating disorder
6. Has donated more than 500ml of blood in the last 3 months prior to the initial laboratory visit
7. Insufficient mental capacity or language skills to independently understand and follow the study protocol
8. Has an irregular sleeping pattern (e.g. due to undertaking night-shift work)
9. Any other condition, concurrent intervention or behaviour deemed either to pose undue personal risk to the participant or to introduce bias into the experiment
18 Years
40 Years
ALL
Yes
Sponsors
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University of Bath
OTHER
Responsible Party
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Guoda Karoblyte
Doctoral Researcher
Locations
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University of Bath
Bath, , United Kingdom
Countries
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Other Identifiers
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0590
Identifier Type: -
Identifier Source: org_study_id
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