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Идёт набор NCT06000774

Therapeutic Ketogenic Diet in Anorexia Nervosa

Без фазы С лечением Anorexia Nervosa in Remission Bulimia Nervosa Anorexia Nervosa

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Therapeutic Ketogenic Diet.
Кому может быть актуально
Состояния в реестре: Anorexia Nervosa in Remission, Bulimia Nervosa, Anorexia Nervosa. Базовые параметры: 18 лет — 45 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Ketogenic Diet in Eating Disorders to Target Metabolism and Normalize Persistent Eating Disorder Psychopathology

Обзор

This study will investigate the effects of therapeutic ketogenic diet (TKD) on eating behavior including drive to restrict, body dissatisfaction, mood and anxiety in individuals with anorexia nervosa who have been weight normalized (body mass index of 17.5 or greater) but continue to struggle with eating disorder behaviors including a high drive for thinness and body dissatisfaction. The Underweight Anorexia Nervosa (AN) Sub-Study will investigate the effects of TKD on eating behavior including drive to restrict, body dissatisfaction, mood and anxiety in individuals with anorexia nervosa who are currently underweight (body mass index between 16.0 and 17.49) and continue to struggle with eating disorder behaviors including a high drive for thinness and body dissatisfaction. The Bulimia Nervosa Pilot will will investigate the effects of TKD on eating behavior including drive to binge and purge, body dissatisfaction, mood and anxiety in individuals with bulimia nervosa.

Подробное описание

For this 14-week study, the investigator will recruit twenty individuals with anorexia nervosa who have been weight normalized but continue to have high impairment from the illness with a high (2 standard deviations above average) drive for thinness and body dissatisfaction and a high drive for food restriction and thus are at high risk for full relapse. Study participants will be carefully assessed and oriented to the ketogenic diet according to the procedures in our small previous trial (Calabrese, et al., 2022). The study will be conducted in a university medical environment, showing feasibility and safety in a typical medical setting. A commercial supplier will provide the ketogenic diet. After ketosis induction over two weeks, study participants will be assessed weekly for ketosis and mood, anxiety, and eating disorder symptoms.

For the BN Pillot study we will also complete a small pilot in 5 individuals with bulimia nervosa.

For the Underweight Anorexia Nervosa (AN) Sub-Study we will also recruit 30 individuals with anorexia nervosa who are mild to moderately underweight and have a body mass index of between 16.0 to 17.49.

Primary Objective 1 is to test the effects of ketogenic diet in individuals with anorexia nervosa who are weight recovered but continue to suffer severely from drive for thinness and are at very high relapse risk. Participants will be evaluated for tolerability of the study and weight trajectory. Primary Objective 2 is to assess improvement in AN symptoms and behaviors in relation to the ketogenic diet over a 12-week course. Participants will be assessed for specific symptoms such as drive for thinness and body dissatisfaction, fear of eating and weight gain. Primary Objective 3 is to assess the underlying genetic basis for the treatment effect of the ketogenic diet.

Bulimia Nervosa Pilot Objective 1: To test the effects of ketogenic diet in individuals with bulimia nervosa.

Bulimia Nervosa Pilot Objective 2: To assess improvement in BN symptoms and behaviors in relation to the ketogenic diet over a 2-week induction period followed by a 12-week course of the intervention. We expect especially a reduction in binge eating episodes and associated purging episodes in response to the treatment and in addition to improvement of the cognitive emotional symptoms.

Underweight AN Sub-Study Objective 1: To test the effects of ketogenic diet in individuals with anorexia nervosa who are currently mildly underweight and assess how the intervention impacts weight normalization in this population.

Underweight AN Sub-Study Objective 2: To assess improvement in AN symptoms and behaviors in relation to the ketogenic diet over a 2-week induction period followed by a 12-week course of the intervention.

Underweight AN Sub-Study Objective 3: To assess the underlying genetic basis for the treatment effect of the ketogenic diet.

Вмешательства

  • Другое Therapeutic Ketogenic Diet
    therapeutic ketogenic diet

Первичные конечные точки

  • To assess the safety and tolerability in individuals with anorexia nervosa who are weight recovered, individuals with anorexia nervosa who are currently underweight, and individuals with bulimia nervosa using weekly body weight measurements. [Срок оценки: Weekly for the duration of the study intervention (14 weeks)]
  • To assess the safety and tolerability in individuals with anorexia nervosa (AN) who are weight recovered, AN individuals who are currently underweight, and Bulimia Nervosa individuals using the Committee of Clinical Investigations UKU-Side Effect Scale [Срок оценки: At weeks 4, 8, 12, 14]
  • Measurement of drive for weight loss, fear of weight gain and body image distortion using the Eating Disorder Examination Questionnaire (EDEQ) Global Score, EDEQ Eating Restraint Score, and EDEQ Weight Concern [Срок оценки: At baseline, Week 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 3 month follow-up]
  • Measurement of the relationship between genotype and improvement of eating disorder symptoms [Срок оценки: At baseline]

Критерии участия

Weight-Recovered AN Inclusion Criteria:

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Persons, aged 18 to 45 years
  • History of anorexia nervosa according to DSM-5 criteria
  • Weight recovered at the time of study inclusion (body mass index > 17.5 kg/m2)
  • Greater or equal to 2 standard deviations scores of eating disorder-relevant behaviors on the Eating Disorder Inventory-3 and Eating Disorder Examination Questionnaire
  • The following types of psychiatric medications are allowed: antidepressant, anxiolytic, atypical antipsychotic, mood stabilizers
  • English is primary spoken language

Weight-Recovered AN Exclusion Criteria:

  • Pregnancy or lactation
  • Electrolyte, blood count, kidney function or liver function abnormalities
  • Psychosis
  • Neurocognitive disorders including dementias or traumatic brain injury that is symptomatic
  • Current alcohol use disorder (AUD) or substance use disorder (SUD) according to DSM-5 criteria
  • Uncontrolled hypertension
  • Hepatic impairment (Class-Pugh b or c)
  • Diabetes mellitus
  • Family history of porphyria
  • History of recent heart attack, vascular disease, or any other current acute medical conditions as determined by the principal investigator
  • Inability or unwillingness to adhere to the TKD diet for the duration of the study
  • Blind or illiterate individuals

Underweight AN Sub-Study Inclusion Criteria:

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Persons, aged 18 to 45 years
  • Anorexia nervosa according to DSM-5 criteria
  • Current Body Mass Index (BMI) at the time of study inclusion of 16.0 to 17.49
  • An elevated EDE-Q global score of 2.09 or greater
  • The following types of psychiatric medications are allowed: antidepressant, anxiolytic, atypical antipsychotic, mood stabilizers
  • English is primary spoken language

Underweight AN Sub-Study Exclusion Criteria:

  • Pregnancy or lactation
  • Electrolyte, blood count, kidney function or liver function abnormalities
  • Psychosis
  • Neurocognitive disorders including dementias or traumatic brain injury that is symptomatic
  • Current alcohol use disorder (AUD) or substance use disorder (SUD) according to DSM-5 criteria
  • Uncontrolled hypertension
  • Hepatic impairment (Class-Pugh b or c)
  • Diabetes mellitus
  • Family history of porphyria
  • History of recent heart attack, vascular disease, or any other current acute medical conditions as determined by the principal investigator
  • Inability or unwillingness to adhere to the TKD diet for the duration of the study
  • Blind or illiterate individuals

Bulimia Nervosa Pilot Inclusion Criteria:

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Persons, aged 18 to 45 years
  • History of bulimia nervosa according to DSM-5 criteria
  • An elevated EDE-Q global score of 2.09 or greater
  • The following types of psychiatric medications are allowed: antidepressant, anxiolytic, atypical antipsychotic, mood stabilizers
  • English is primary spoken language

Bulimia Nervosa Pilot Exclusion Criteria:

  • Pregnancy or lactation
  • Electrolyte, blood count, kidney function or liver function abnormalities
  • Psychosis
  • Neurocognitive disorders including dementias or traumatic brain injury that is symptomatic
  • Current alcohol use disorder (AUD) or substance use disorder (SUD) according to DSM-5 criteria
  • Uncontrolled hypertension
  • Hepatic impairment (Class-Pugh b or c)
  • Diabetes mellitus
  • Family history of porphyria
  • History of recent heart attack, vascular disease, or any other current acute medical conditions as determined by the principal investigator
  • Inability or unwillingness to adhere to the TKD diet for the duration of the study
  • Blind or illiterate individuals

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

США · 1 центр
  • University of California San Diego — San Diego

Публикации

  • Scolnick B, Zupec-Kania B, Calabrese L, Aoki C, Hildebrandt T. Remission from Chronic Anorexia Nervosa With Ketogenic Diet and Ketamine: Case Report. Front Psychiatry. 2020 Jul 30;11:763. doi: 10.3389/fpsyt.2020.00763. eCollection 2020. PMID 32848935
  • Frank GKW, Shott ME, DeGuzman MC. The Neurobiology of Eating Disorders. Child Adolesc Psychiatr Clin N Am. 2019 Oct;28(4):629-640. doi: 10.1016/j.chc.2019.05.007. Epub 2019 Jul 4. PMID 31443880
  • Frank GKW, Shott ME, Stoddard J, Swindle S, Pryor TL. Association of Brain Reward Response With Body Mass Index and Ventral Striatal-Hypothalamic Circuitry Among Young Women With Eating Disorders. JAMA Psychiatry. 2021 Oct 1;78(10):1123-1133. doi: 10.1001/jamapsychiatry.2021.1580. PMID 34190963
  • Dignon A, Beardsmore A, Spain S, Kuan A. 'Why I won't eat': patient testimony from 15 anorexics concerning the causes of their disorder. J Health Psychol. 2006 Nov;11(6):942-56. doi: 10.1177/1359105306069097. PMID 17035265
  • Calabrese L, Scolnick B, Zupec-Kania B, Beckwith C, Costello K, Frank GKW. Ketogenic diet and ketamine infusion treatment to target chronic persistent eating disorder psychopathology in anorexia nervosa: a pilot study. Eat Weight Disord. 2022 Dec;27(8):3751-3757. doi: 10.1007/s40519-022-01455-x. Epub 2022 Aug 23. PMID 35997954
  • Frank GKW, Scolnick B, Beckwith C, Shott ME, Kilty S, Swindle S, Lutter M, Rho JM. Symptom impact and safety of ketogenic therapy in adults with anorexia nervosa: a feasibility trial. Commun Med (Lond). 2026 Jun 3;6(1):315. doi: 10.1038/s43856-026-01644-0. PMID 42236862

Идентификаторы

NCT: NCT06000774 · 807674

Первоисточники (государственные реестры)

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