Ketogenic Diet in the Treatment of PTSD in Germany: A Single-Arm Feasibility Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 6
- 试验地点
- 2
- 主要终点
- Process Feasibility
研究概览
简要总结
This project is a prospective, single-arm, open-label feasibility study testing whether a 12-week medically supervised ketogenic diet (KD) can be implemented in adults with PTSD in Germany (N=6). The primary aim is feasibility: recruitment (N=6 within a predefined timeframe), adherence to ketosis measured by daily capillary β-hydroxybutyrate (BHB), completion of study assessments (including daily EMA symptom/BHB reporting), and retention through the post-intervention visit. Secondary outcomes include participant self-reported feasibility at week 12. Exploratory outcomes include descriptive changes in PTSD symptoms/mental health and metabolic/inflammatory/mitochondrial biomarkers as well as associations between biomarkers and PTSD symptoms. The study is not powered for efficacy; results will inform the design of a larger clinical trial.
详细描述
Post-traumatic stress disorder (PTSD) is characterized by intrusive re-experiencing of traumatic events and clinically relevant impairments in mood and functioning. In Germany, PTSD affects a meaningful proportion of the general population and is particularly prevalent in refugee populations. Although trauma-focused psychotherapies are considered first-line treatments, many patients face access barriers and high dropout rates, and currently available pharmacological approaches show limited remission rates.
Emerging evidence suggests that PTSD is associated with trauma-related metabolic dysregulation, including inflammatory processes and mitochondrial impairments. Ketogenic therapy - most commonly implemented via a ketogenic diet (KD) - is a metabolic intervention with documented neuroprotective and anti-inflammatory properties and early evidence of benefit across several psychiatric conditions. Given the overlap between proposed KD mechanisms and PTSD pathophysiology, evaluating KD as a potential intervention for PTSD is a promising and novel research direction. However, prospective feasibility data in German PTSD cohorts are currently lacking, which justifies a human pilot trial under real-world clinical conditions.
This study is a 12-week, single-arm, open-label feasibility trial in six adults with verified PTSD living in Germany. The primary objective is to evaluate feasibility with respect to recruitment, adherence to ketosis, completion of study assessments, and retention. Secondary objectives assess participant-reported feasibility. Exploratory objectives include changes in PTSD symptoms and general mental health, associations between daily capillary β-hydroxybutyrate (BHB) levels and daily symptom severity, identification of barriers and facilitators relevant to future trials, and descriptive changes in metabolic, inflammatory, and mitochondrial markers. Participants will receive a medically supervised, individually tailored KD with structured dietary support. Adherence and symptom trajectories will be monitored via daily BHB measurements and brief daily self-reports.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Mental capacity to provide informed consent
- •Provides written confirmation of informed consent
- •Adults (18-65 years)
- •Verified PTSD diagnosis according to DSM 5-TR or ICD-11
- •Currently living in Germany
- •High treatment motivation (score > 7/10)
- •Consent to information sharing within study staff (release from medical confidentiality)
- •No medical or psychiatric contraindication
排除标准
- •Pregnant or breastfeeding
- •Active alcohol or drug misuse
- •BMI < 18.5
- •Currently medicated with glucocorticoids, lithium, anticonvulsants, hypertension medication, glucose-lowering medications, or SGLT-2 inhibitor medications
- •Diagnosed with type 1 or type 2 diabetes
- •Diagnosed with severely impaired kidney function
- •Diagnosed with ESLD (End Stage Liver Disease) or ESRD (End Stage Renal Disease)
- •Follows a vegan diet
- •History of eating disorders
- •Acute or chronic suicidality
- •Acute or chronic self-injury behavior
- •Acute positive psychotic/manic symptomatology
- •Already following a ketogenic diet within the past 6 weeks
- •Any change to psychiatric medication regimen in past 6 weeks
- •Severe hypercholesterolemia (may represent genetic metabolic disorder)
- •Porphyria, heart failure, pancreatitis
- •Institutionally dependent individuals
研究组 & 干预措施
Ketogenic dietary intervention
干预措施: Ketogenic diet (Other)
结局指标
主要结局
Process Feasibility
时间窗: Intervention: 12 weeks
The primary endpoints assess feasibility based on recruitment success, adherence to the ketogenic intervention, completion of study assessments, and participant retention over the 12-week intervention period.
次要结局
- Self-report feasibility(Intervention: 12 weeks)
研究者
Robin Engelhardt
Principal Investigator
Bundeswehr University Munich
