The Potential of a Low Glutamate Diet as a Treatment for Pediatric Epilepsy
Primary Purpose
Epilepsy in Children, Epilepsy in Youth, Randomized Controlled Trial
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Low Glutamate diet
Sponsored by
About this trial
This is an interventional treatment trial for Epilepsy in Children
Eligibility Criteria
Inclusion Criteria:
- 4 or more seizures per month
- Willing to keep all medications constant during the study.
- All medications have remained constant for 30 days prior to study enrollment
- Any previously attempted dietary therapies stopped before study enrollment
Exclusion Criteria:
- Known or suspected inborn errors of metabolism
- Non-English speaking households
Sites / Locations
- American University
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Wait-listed control
Low Glutamate diet
Arm Description
Participants continue care as usual. All all medications must be kept constant during the study period, unless medically necessary.
Participants are put on the low glutamate diet for one month. The low glutamate diet reduces the consumption of free glutamate, while optimizing dietary micronutrient and antioxidant intake.
Outcomes
Primary Outcome Measures
Change in seizure frequency
All families will keep a seizure diary recording the number of daily seizures. This will be used to accurately determine these variables for the last week, which will be recorded on seizure assessment forms.
Change in seizure severity
. During the last week of each study period, families will be asked to complete a seizure assessment form. This will include a subjective rating scale for seizure severity with a minimum score of 0 (not severe) and a maximum score of 10 (very severe).
Change in seizure duration
All families will keep a seizure diary recording the duration of seizures. This will be used to accurately determine these variables for the last week, which will be recorded on seizure assessment forms.
Secondary Outcome Measures
The effect of a 1-month low-glutamate diet on quality of life in children with epilepsy.
Parents will be asked to complete the Quality of Life in Childhood Epilepsy Questionnaire (QOLCE-55). This 55-question quality of life questionnaire has been validated for children ages 4 and older and is used to assess the participant's cognitive, emotional, social, and physical functioning.
The effect of a 1-month low-glutamate diet on cognitive functioning in children with epilepsy.
Cognitive function will be assessed via CNSVS, a computerized neurocognitive testing software.
Examine change in resting state brain waves after 1-month on the low glutamate diet
Electroencephalography (EEG) will be offered to all participants. Four minutes of eyes-closed and eyes-open resting state EEG data will be recorded at the end of the baseline, wait-listed control, and active intervention periods in a sound-attenuated, air-conditioned room. Participants will sit in a comfortable chair in front of a computer monitor. For eyes-closed recordings, participants will be instructed to sit as still as possible, while staying relaxed but awake. For eyes-open recordings, participants will be instructed to sit as still as possible and to focus on a fixation point on the screen while keeping blinking to a minimum, if possible. Participants will be monitored to make sure they are complying with condition instructions. Mean power (total power of frequency band/width of frequency band) and relative power (absolute power of frequency band/total power or percent) will be calculated for delta, theta, alpha, beta, gamma, high gamma, and total power.
Full Information
NCT ID
NCT04545346
First Posted
August 26, 2020
Last Updated
July 18, 2022
Sponsor
American University
Collaborators
Children's National Research Institute
1. Study Identification
Unique Protocol Identification Number
NCT04545346
Brief Title
The Potential of a Low Glutamate Diet as a Treatment for Pediatric Epilepsy
Official Title
The Potential of a Low Glutamate Diet in Refractory Pediatric Epilepsy Patients
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
October 15, 2020 (Actual)
Primary Completion Date
June 15, 2022 (Actual)
Study Completion Date
June 15, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
American University
Collaborators
Children's National Research Institute
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 study is investigating if following the low glutamate diet for 1 month, as compared to care as usual, can improve seizure frequency, severity, and duration; cognitive functioning; and/or quality of life in children with epilepsy.
Detailed Description
Epilepsy is estimated to effect 470,000 children within the U.S. About a third of epilepsy patients are refractory. For these patients, dietary therapy is an alternative option. However, current dietary therapies present issues with compliance, palatability, adverse events, and providing necessary nutrients for brain growth and development during childhood. A dietary option that can improve tolerability, increase compliance, and reduce or eliminate adverse effects, while also optimizing nutrient intake, is critical for the advancement of dietary therapy options in epilepsy.
Glutamate is found in the diet as a flavor enhancer; and is also an important neurotransmitter in the body which mediates seizure activity. Dietary sources of free glutamate are common and include numerous food additives (including many hidden sources) and some items which naturally contain higher amounts of glutamate. The low glutamate diet reduces the consumption of free glutamate, while optimizing dietary micronutrient and antioxidant intake, which can protect against the negative effects caused by high glutamate concentrations in the brain. Additionally, the low glutamate diet is balanced, nutritious and palatable, with no side effects.
The study is investigating if following the low glutamate diet for 1 month can improve seizure frequency, severity, and duration; cognitive functioning; and/or quality of life, in children with epilepsy. Participation in the study will be done virtually and over a 2- or 3- month study period, depending on group randomization. All participants will have the opportunity to undergo dietary training and follow the diet.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Epilepsy in Children, Epilepsy in Youth, Randomized Controlled Trial, Refractory Epilepsy, Diet Intervention
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
45 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Wait-listed control
Arm Type
No Intervention
Arm Description
Participants continue care as usual. All all medications must be kept constant during the study period, unless medically necessary.
Arm Title
Low Glutamate diet
Arm Type
Experimental
Arm Description
Participants are put on the low glutamate diet for one month. The low glutamate diet reduces the consumption of free glutamate, while optimizing dietary micronutrient and antioxidant intake.
Intervention Type
Other
Intervention Name(s)
Low Glutamate diet
Intervention Description
Participants will be given extensive online dietary training and assigned to follow the low glutamate diet for one month. The low glutamate diet reduces the consumption of free glutamate, while optimizing dietary micronutrient and antioxidant intake.
Primary Outcome Measure Information:
Title
Change in seizure frequency
Description
All families will keep a seizure diary recording the number of daily seizures. This will be used to accurately determine these variables for the last week, which will be recorded on seizure assessment forms.
Time Frame
At 1 month post treatment
Title
Change in seizure severity
Description
. During the last week of each study period, families will be asked to complete a seizure assessment form. This will include a subjective rating scale for seizure severity with a minimum score of 0 (not severe) and a maximum score of 10 (very severe).
Time Frame
At 1 month post treatment
Title
Change in seizure duration
Description
All families will keep a seizure diary recording the duration of seizures. This will be used to accurately determine these variables for the last week, which will be recorded on seizure assessment forms.
Time Frame
At 1 month post treatment
Secondary Outcome Measure Information:
Title
The effect of a 1-month low-glutamate diet on quality of life in children with epilepsy.
Description
Parents will be asked to complete the Quality of Life in Childhood Epilepsy Questionnaire (QOLCE-55). This 55-question quality of life questionnaire has been validated for children ages 4 and older and is used to assess the participant's cognitive, emotional, social, and physical functioning.
Time Frame
At 1 month post treatment
Title
The effect of a 1-month low-glutamate diet on cognitive functioning in children with epilepsy.
Description
Cognitive function will be assessed via CNSVS, a computerized neurocognitive testing software.
Time Frame
At 1 month post treatment
Title
Examine change in resting state brain waves after 1-month on the low glutamate diet
Description
Electroencephalography (EEG) will be offered to all participants. Four minutes of eyes-closed and eyes-open resting state EEG data will be recorded at the end of the baseline, wait-listed control, and active intervention periods in a sound-attenuated, air-conditioned room. Participants will sit in a comfortable chair in front of a computer monitor. For eyes-closed recordings, participants will be instructed to sit as still as possible, while staying relaxed but awake. For eyes-open recordings, participants will be instructed to sit as still as possible and to focus on a fixation point on the screen while keeping blinking to a minimum, if possible. Participants will be monitored to make sure they are complying with condition instructions. Mean power (total power of frequency band/width of frequency band) and relative power (absolute power of frequency band/total power or percent) will be calculated for delta, theta, alpha, beta, gamma, high gamma, and total power.
Time Frame
At 1 month post treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
4 or more seizures per month
Willing to keep all medications constant during the study.
All medications have remained constant for 30 days prior to study enrollment
Any previously attempted dietary therapies stopped before study enrollment
Exclusion Criteria:
Known or suspected inborn errors of metabolism
Non-English speaking households
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kathleen Holton, MPH, PhD
Organizational Affiliation
American University
Official's Role
Principal Investigator
Facility Information:
Facility Name
American University
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20016
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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The Potential of a Low Glutamate Diet as a Treatment for Pediatric Epilepsy
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