search
Back to results

IF-MCT 16:8: Investigating the Influence of Intermittent Fasting With and Without MCTs in Patients With Drug-resistant Epilepsy (IF-MCT16:8)

Primary Purpose

Epilepsy, Intermittent Fasting

Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
IF 16:8 as active comparator vs. IF MCT 16:8 as experimental arm
Sponsored by
University Hospital Marburg
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Epilepsy focused on measuring Drug-resistant epilepsy, Intermittent fasting, Seizure frequency, Biomarkers, Neural networks, Microbiome

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Subjects able to provide informed consent Drug-resistant epilepsy At least 3 seizures per month Exclusion Criteria: Pregnancy Breast feeding period Metabolic disorder (e.g. diabetes, liver cirrhosis, kidney disease) Eating Disorder (e.g. anorexia, bulimia) Chronic inflammatory gut disease Active cancerous disease Antibiotics within the last 3 months

Sites / Locations

  • Philipps University Marburg, Faculty of Medicine, Department of Neurology, Epilepsy CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

IF 16:8

IF MCT 16:8

Arm Description

12 weeks intermittent fasting according to the 16:8 method (IF 16:8)

12 weeks intermittent fasting with additional intake of exogenous MCTs (IF MCT 16:8)

Outcomes

Primary Outcome Measures

Effect of intermittent fasting according to the 16:8 method with and without exogenous MCTs on seizure frequency in drug-resistant epilepsy
Monthly seizure frequency is recorded using standardized seizure diaries.

Secondary Outcome Measures

Effect of intermittent fasting according to the 16:8 method on therapy adherence in patients with drug-resistant epilepsy
The nutritional behavior during the studio is recorded using a standardized daily nutrition diary.
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on ketosis in patients with drug-resistant epilepsy
All participants measure their ketosis weekly with a standardized ketosis device during the fasting episode and document this in a ketosis table provided.
Effect of intermittent fasting according to the 16:8 method on self-efficacy in patients with drug-resistant epilepsy
Self-efficacy is determined using the scale of general self-efficacy expectation (Jerusalem & Schwarzer). This includes 10 items with 4 degrees. High scores mean a high level of general self-efficacy expectation.
Effect of intermittent fasting according to the 16:8 method on life-quality in patients with drug-resistant epilepsy
Life-quality is measured using the standardized questionnaire on life quality.
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on biomarkers in patients with drug-resistant epilepsy
The metabolome is examined using a mass spectroscopic blood sample. The microbiome is examined using a standardized stool sample using next-generation sequencing.
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on neural networks in patients with drug-resistant epilepsy
Neural networks are measured using magnetic resonance imaging (diffusion tensor imaging and resting state MRI).
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on immune status in patients with drug-resistant epilepsy
The immune status and in particular the T-cell mediated innate immune response is determined serologically.
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on fatigue in patients with drug-resistant epilepsy
Fatigue is measured using the standardized Fatigue-Impact-Scale (FIS)-Test.
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on attention in patients with drug-resistant epilepsy
Attention is measured using the standardized test battery for attention testing (TAP-Test).
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on neurotransmitter gamma-aminobutyric acid (GABA)in patients with drug-resistant epilepsy
The change in the neurotransmitter GABA is examined serologically over the period of the study phase.
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on stress response in patients with drug-resistant epilepsy
Stress response in hair cortisol of all participants is recorded using several hair samples.
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on intima media thickness in patients with drug-resistant epilepsy
Intima media thickness of all participants will be recorded with a duplex sonographic examination of the arteries supplying the brain.

Full Information

First Posted
August 8, 2023
Last Updated
August 24, 2023
Sponsor
University Hospital Marburg
search

1. Study Identification

Unique Protocol Identification Number
NCT06013761
Brief Title
IF-MCT 16:8: Investigating the Influence of Intermittent Fasting With and Without MCTs in Patients With Drug-resistant Epilepsy
Acronym
IF-MCT16:8
Official Title
Monocentric Randomized Experimental Pilot Trial Investigating the Influence of Intermittent Fasting According to the 16:8 Method With and Without Medium-chain Triglycerides (MCTs) on Seizure Frequency, Biomarkers and Neural Networks in Patients With Drug-resistant Epilepsy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 25, 2023 (Actual)
Primary Completion Date
December 31, 2025 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Marburg

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of the prospective monocentric pilot trial is to investigate the influence of intermittent fasting with or without a once-daily intake with medium chain triglycerides (MCTs) on the frequency of seizures in patients with therapy-refractory epilepsy. The effects of 12 weeks intermittent fasting according to the 16:8 method (IF 16:8) are compared to 12 weeks intermittent fasting with additional intake of exogenous MCTs (IF MCT 16:8) in a within-subject-crossover-design in 28 patients with drug-resistant epilepsy.
Detailed Description
One in three patients suffering epilepsy does not become seizure-free with conventional pharmacotherapy. The chance of seizure freedom with each additional medication is only in the single-digit percentage range. For this reason, additive therapies such as the ketogenic diet play an important role. By means of a ketogenic diet, a significant reduction in the frequency of seizures has been shown in various studies for children. The main goal is the body's own production of ketone bodies in the liver, which are used instead of glucose to produce the energy carrier ATP. This metabolic change results in biochemical, metabolic and hormonal changes that may reduce the severity and frequency of epileptic seizures, although the exact mechanisms are not yet understood. Common to all forms of ketogenic diets (e.g. classic kKD, modified Atkins diet, low glycemic index diet) is a specific preparation of each meal with plans for meals and often an initiation of additive therapy in the inpatient setting or by trained staff. Especially in adulthood, the lack of treatment adherence seems to play an important role in the effectiveness of the ketogenic diet. A form of ketogenic diet which might be more suitable for everyday use is intermittent fasting. The primary aim of the prospective monocentric pilot trial is to investigate the effect of intermittent fasting with and without a once-daily intake of medium-chain triglycerides (MCTs) on the frequency of seizures in patients with therapy-refractory epilepsy. The effects of 12 weeks intermittent fasting according to the 16:8 method (IF 16:8) are compared to 12 weeks intermittent fasting with additional intake of exogenous medium chain triglycerides (IF MCT 16:8) in a within-subject-crossover design in 28 patients with drug-resistant epilepsy. Secondarily, the influence of this diet on the composition of the gut microbiome, the T-cell mediated innate immune system and neuronal signalling pathways and networks will be investigated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Epilepsy, Intermittent Fasting
Keywords
Drug-resistant epilepsy, Intermittent fasting, Seizure frequency, Biomarkers, Neural networks, Microbiome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
28 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
IF 16:8
Arm Type
Active Comparator
Arm Description
12 weeks intermittent fasting according to the 16:8 method (IF 16:8)
Arm Title
IF MCT 16:8
Arm Type
Experimental
Arm Description
12 weeks intermittent fasting with additional intake of exogenous MCTs (IF MCT 16:8)
Intervention Type
Other
Intervention Name(s)
IF 16:8 as active comparator vs. IF MCT 16:8 as experimental arm
Intervention Description
12 weeks intermittent fasting according to the 16:8 method (IF 16:8) are compared with 12 weeks intermittent fasting with additional intake of exogenous MCTs (IF MCT 16:8) in a within-subject-crossover design in 28 patients with drug-resistant epilepsy. In order to enable the highest possible adherence, there are no restrictions on the composition of the food.
Primary Outcome Measure Information:
Title
Effect of intermittent fasting according to the 16:8 method with and without exogenous MCTs on seizure frequency in drug-resistant epilepsy
Description
Monthly seizure frequency is recorded using standardized seizure diaries.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Effect of intermittent fasting according to the 16:8 method on therapy adherence in patients with drug-resistant epilepsy
Description
The nutritional behavior during the studio is recorded using a standardized daily nutrition diary.
Time Frame
3 months
Title
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on ketosis in patients with drug-resistant epilepsy
Description
All participants measure their ketosis weekly with a standardized ketosis device during the fasting episode and document this in a ketosis table provided.
Time Frame
3 months
Title
Effect of intermittent fasting according to the 16:8 method on self-efficacy in patients with drug-resistant epilepsy
Description
Self-efficacy is determined using the scale of general self-efficacy expectation (Jerusalem & Schwarzer). This includes 10 items with 4 degrees. High scores mean a high level of general self-efficacy expectation.
Time Frame
3 months
Title
Effect of intermittent fasting according to the 16:8 method on life-quality in patients with drug-resistant epilepsy
Description
Life-quality is measured using the standardized questionnaire on life quality.
Time Frame
3 months
Title
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on biomarkers in patients with drug-resistant epilepsy
Description
The metabolome is examined using a mass spectroscopic blood sample. The microbiome is examined using a standardized stool sample using next-generation sequencing.
Time Frame
3 months
Title
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on neural networks in patients with drug-resistant epilepsy
Description
Neural networks are measured using magnetic resonance imaging (diffusion tensor imaging and resting state MRI).
Time Frame
3 months
Title
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on immune status in patients with drug-resistant epilepsy
Description
The immune status and in particular the T-cell mediated innate immune response is determined serologically.
Time Frame
3 months
Title
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on fatigue in patients with drug-resistant epilepsy
Description
Fatigue is measured using the standardized Fatigue-Impact-Scale (FIS)-Test.
Time Frame
3 months
Title
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on attention in patients with drug-resistant epilepsy
Description
Attention is measured using the standardized test battery for attention testing (TAP-Test).
Time Frame
3 months
Title
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on neurotransmitter gamma-aminobutyric acid (GABA)in patients with drug-resistant epilepsy
Description
The change in the neurotransmitter GABA is examined serologically over the period of the study phase.
Time Frame
3 months
Title
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on stress response in patients with drug-resistant epilepsy
Description
Stress response in hair cortisol of all participants is recorded using several hair samples.
Time Frame
3 months
Title
Effect of intermittent fasting according to the 16:8 method with exogenous MCTs on intima media thickness in patients with drug-resistant epilepsy
Description
Intima media thickness of all participants will be recorded with a duplex sonographic examination of the arteries supplying the brain.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects able to provide informed consent Drug-resistant epilepsy At least 3 seizures per month Exclusion Criteria: Pregnancy Breast feeding period Metabolic disorder (e.g. diabetes, liver cirrhosis, kidney disease) Eating Disorder (e.g. anorexia, bulimia) Chronic inflammatory gut disease Active cancerous disease Antibiotics within the last 3 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wiebke Hahn, MD
Phone
+49 642158 65348
Email
Hahnwi@staff.uni-marburg.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wiebke Hahn, MD
Organizational Affiliation
Philipps University Marburg Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Philipps University Marburg, Faculty of Medicine, Department of Neurology, Epilepsy Center
City
Marburg
State/Province
Hessen
ZIP/Postal Code
Baldingerstr., 35043
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Department of Neurology, Epilepsy Center
Phone
+49 6421 5865348
Email
ezm@med.uni-marburg.de

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

IF-MCT 16:8: Investigating the Influence of Intermittent Fasting With and Without MCTs in Patients With Drug-resistant Epilepsy

We'll reach out to this number within 24 hrs