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Ketogenic Diet - a Randomized, Controlled, Cross-over Study

A Randomized Controlled Diet Intervention Comparing Effects of a Ketogenic Diet Versus a National Food Administration Recommended Diet Among Healthy Female Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02417350
Enrollment
24
Registered
2015-04-15
Start date
2015-04-30
Completion date
2015-10-31
Last updated
2015-11-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Brief summary

The investigators planned study is a randomized, controlled exploratory study of a ketogenic and a NFA (National Food Administration) recommended diet. Study participants will be female nutrition students with both knowledge and interest in dietary surveys, in order to increase motivation and adherence. They will be provided with cooked food. The women should be weight stable and maintain their physical activity during the study, in order to evaluate how the diet itself affects various health parameters. The investigators intend to investigate diet specific biomarkers (small molecules involved in metabolism) in the blood, as well as blood lipids, body composition, gut microbiota, energy substrate utilization, exercise performance, resting metabolic rate, hormones, cognition and sweet cravings. In addition, the investigators intend to qualitatively study the experience of following both of these dietary regimes. The investigators intend to make a short and controlled study. The study is expected to reveal whether the ketogenic diet is a healthy or unhealthy diet in the short term. The investigators also expect that data from this study will be a helpful tool to measure diet adherence in future long-term studies.

Detailed description

Aim: The aim of this randomized controlled exploratory study is to study effects of a ketogenic diet (a low carb - high fat (LCHF) diet) compared to a National Food Administration (NFA) recommended diet (NNR2012). Primary outcomes are blood lipids and diet specific biomarkers. Power calculations show that 20 participants are needed to obtain significant results with 90% power at the 95% significance level for the primary outcome small-dense LDL (blood lipids). The investigators calculate that 20% of the participants will drop out before the end of the study, and therefore the investigators aim to recruit a total of 24 participants. Secondary outcomes are body composition, gut microbiota, energy substrate utilization, exercise performance, resting metabolic rate (RMR), hormones, cognition, sweet cravings, and the experience of following the two dietary regimes. Study design: Study participants will be female nutrition students with both knowledge and interest in dietary surveys, in order to increase motivation and adherence. The women should be weight stable and maintain their physical activity during the study, in order to evaluate how the diet itself affects various health parameters. Study participants will be provided with all food in the diet intervention. The amount and source of fat, protein and carbohydrates in the two diets are strictly defined; LCHF: Maximum 25 g carbohydrates/day (approximately 5 E%), 20 E% protein and 75 E% fat (35 E% saturated fat). NNR2012: 50 E% carbohydrates, 20 E% protein and 30 E% fat (10 E% saturated fat). Study participants will be randomized with respect to their physical activity level to one of two study arms, with crossover design: Study arm 1: LHCF (4 weeks) --- washout (15 weeks) --- NNR (4 weeks) Study arm 2: NNR (4 weeks) --- washout (15 weeks) --- LCHF (4 weeks) Study participants will eat each diet for four weeks. The different diets are separated by a washout period when they eat as usual. Every morning during each four-week diet period the participants will measure their urine ketones by using urine ketone strips, weigh themselves and record their body weight. Any discrepancies in food intake will be recorded in a log book in which also the daily physical activity level is specified. Energy expenditure will be measured for three days during the four week periods using SenseWear activity meter (a validated and objective method) to see if energy intake matches energy expenditure. Baseline- and outcome measurements will be performed prior to and at the end of each four-week diet period. Qualitative measurements: When the whole diet study is completed and the research subjects have experience of eating both NNR and LCHF diet interviews will be conducted with some of the research subjects. The study is expected to reveal whether LCHF is a healthy or unhealthy diet in the short term. The investigators also expect that data from this study will be a helpful tool to measure diet adherence in future long-term studies.

Interventions

OTHERKetogenic diet for four weeks, then a 15 week washout, and finally a NFA recommended diet for four weeks
OTHERNFA recommended diet for four weeks, then a 15 week washout, and finally a ketogenic diet for four weeks.

Sponsors

Umeå University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

* Female * Age 18-30 * BMI 18,5-25

Exclusion criteria

* Waist circumference ≥80 cm * Gravidity * Diabetes * Thyroid disease * Prescribed medication for high cholesterol or high blood pressure * Nicotine use * Eating disorder * Dietary restrictions

Design outcomes

Primary

MeasureTime frameDescription
Biomarkers in blood Measured with gaschromatography (GC)-time-of-flight/mass spectrometry (MS) and Bio-Plex Assaysbaseline - four weeksMeasured with gaschromatography (GC)-time-of-flight/mass spectrometry (MS) and Bio-Plex Assays
Blood lipids Measured with LipoPrint Systembaseline - four weeksMeasured with LipoPrint System

Secondary

MeasureTime frameDescription
Energy substrate utilization during submaximal exercise Measured with indirect calorimetry during ergometer cycling, lactate in blood.baseline - four weeksMeasured with indirect calorimetry during ergometer cycling, lactate in blood.
Exercise performancebaseline - four weeksCycling at a sub-maximal work rate with increments every 4 min for three periods, thereafter increased work rate every minute until voluntary exhaustion.
Hand grip endurancebaseline - four weeksHand grip test.
Resting metabolic rate Measured with indirect calorimetrybaseline - four weeksMeasured with indirect calorimetry (Quark RMR, COSMED)
Body composition Measured with DXA (Dual Energy X-Ray Absorptiometry)baseline - four weeksMeasured with DXA (Dual Energy X-Ray Absorptiometry)
Cognition Measured with the Stroop color-word testbaseline - four weeksMeasured with the Stroop color-word test
Sweet cravings Measured with a likert scale questionnairebaseline - four weeksMeasured with a likert scale questionnaire
Mood and appetite Measured with a likert scale questionnairebaseline - every third day during the diet intervention period - four weeksMeasured with a likert scale questionnaire
Experiences of following a particular dietary regime measured with Semi-structured interviews analyzed with content analysisAfter finishing both study armsSemi-structured interviews analyzed with content analysis
Hormones Measured with Bio-Plex Assays and ELISAbaseline - four weeksMeasured with Bio-Plex Assays and ELISA
Gut microbiota measured with High-throughput sequencing of nucleic acids (DNA/RNA), short-chain fatty acidsbaseline - four weeksHigh-throughput sequencing of nucleic acids (DNA/RNA), short-chain fatty acids

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026