Validation of an Italian Questionnaire of Adherence to the Ketogenic Diet

Epilepsy Clinical Trial

— iKETOCHECK  

Official title:

Validation of an Italian Questionnaire of Adherence to the Ketogenic Diet: iKetoCheck

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT05377762
• Other study ID #: iKETOCHECK
• Status: Enrolling by invitation
• Start date: March 16, 2022
• Est. completion date: September 2022

Study information

• Verified date: May 2022
• Source: University of Pavia
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The ketogenic diet (KD) represents an effective and safe non-drug treatment for drug-resistant epilepsy in pediatric and adult age based on normocaloric, hyperlipidic (80-90% of the daily energy), normoproteic and hypoglucidic dietary regimen. Adherence to treatment with KD is often difficult in the long term, for the patient and for caregivers, especially in adolescence. There are no tools in the literature other than monitoring ketonemia to measure adherence to the diet. A quality tool, validated by experts, on a large population, would allow for a more solid assessment of adherence to treatment, facilitating clinicians in the interpretation of efficacy results and in implementing an early intervention to adjust the therapy.

Description:

The ketogenic diet (KD) represents an effective and safe non-drug treatment for drug-resistant epilepsy in pediatric and adult age and is the gold standard therapy for type I glucose transporter deficiency syndrome (GLUT1 DS). According to international guidelines, once undertaken, the KD must be continued for at least three months in order to determine its effectiveness and can be continued for years if effective.

In summary, KD is a normocaloric, hyperlipidic (80-90% of the daily energy), normoproteic and hypoglucidic dietary regimen that determines in the organism a state of ketosis similar to that induced by a prolonged fast, which corresponds to average levels of ketonemia equal to 2.5 mmol / L.

Not being able to estimate the concentration of ketone bodies in the brain, the serum measurement is adopted, i.e. the detection of capillary ketonemia. It is important to consider the presence of inter-individual and intra-individual variability of ketonemia and this can be influenced by various factors in addition to the composition of the diet and the ketogenic ratio (fat / protein + carbohydrates): infectious episodes, physical activity, hydration , steroid therapy. Hence the importance of individualized treatment and careful monitoring of adherence to dietary recommendations. The quality of the diet, especially at the beginning of ketogenic therapy, but during the entire follow-up, is essential for achieving optimal levels of ketosis.However, adherence to treatment with KD is often difficult in the long term, for the patient and for caregivers, especially in adolescence. Failure to adhere to KD is mainly attributed to dietary side effects, psychosocial factors, or the dietary restriction itself.

There are no tools in the literature other than monitoring ketonemia to measure adherence to the diet; usually, clinicians ask parents and patients to share the food diary in order to check the calorie intake, the ketogenic ratio and the nutritional composition of the diet. A 'Keto-check' questionnaire was recently developed and validated in Brazil, currently only available in Portuguese, with the aim of providing a tool to measure adherence to the ketogenic diet through simple, easily reproducible questions. A quality tool, validated by experts, on a large population, would allow for a more solid assessment of adherence to treatment, facilitating clinicians in the interpretation of efficacy results and in implementing an early intervention to adjust the therapy.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 105
• Est. completion date: September 2022
• Est. primary completion date: July 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A to 60 Years

Eligibility

Inclusion Criteria:

• Age <60 years

• Gender: both sexes

• Route of administration of the diet: totally or partially oral

• Diagnosis: drug-resistant epilepsy or GLUT1 deficiency

• Duration of treatment with the ketogenic diet: at least 3 months

• Informed consent of the patient and / or an authorized caregiver / legal representative•

Exclusion Criteria:

• Age > 60 years

• Route of administration of the exclusively enteral or parenteral diet

• Duration of treatment with KD less than 3 months

Related Conditions & MeSH terms

• Epilepsy

Locations

Country	Name	City	State
Italy	Center for Childhood and Adolescent Epileptology of the Mondino Foundation	Pavia
Italy	University of Pavia	Pavia

Sponsors (2)

Lead Sponsor	Collaborator
University of Pavia	University of Sao Paulo

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Adherence score	The answer of questionnaire will generate a score. Minimum value will be 10 points and maximum 50 points. Higher scores mean a better outcome.	Through study completion, an average of 6 months