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临床试验/NCT07570875
NCT07570875尚未招募不适用

Evaluating the Impact of Ketogenic Therapy on Symptom Severity and Metabolic Side Effect Profile Among Individuals Living With Bipolar Disorder in A Rural Southern Catchment Area - A Four-Arm Pilot Study

University of Alabama at Birmingham1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2026年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
100
试验地点
1
主要终点
Impact on Symptom Severity as measured by Young Mania Ratings Scale

研究概览

简要总结

It is the purpose of this pilot study to evaluate a high-fat/low-carbohydrate "ketogenic" diet-based intervention as an adjunctive strategy for impacting symptoms of bipolar disorder. The study is designed to evaluate this impact in the rural southern catchment area around Montgomery, Alabama.

While existing access and cost barriers can prevent effective treatment of bipolar disorder in the rural south, using food as medicine represents a possible alternative/adjunctive to traditional high-cost/low-access medications. Specifically, this study will evaluate the impact of combining a ketogenic diet with existing treatment options, under the conditions of the rural catchment area, to determine the impact and efficacy of this intervention at patient and systems levels.

If effective, the interventions examined in this pilot study may increase the efficacy, availability and access to care experienced by individuals living with bipolarity in the rural Deep South.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Verified Bipolar Diagnosis per NETSCID

排除标准

  • Acute psychiatric instability (manic episode, active suicidality requiring hospitalization)
  • Pregnancy
  • Severe renal insufficiency
  • Hepatic insufficiency

研究组 & 干预措施

Long-acting injectable medication + ketogenic diet

Experimental

Participants in this arm will receive long-acting injectable medication for bipolar disorder, plus foodstuffs necessary to support ketogenic diet. The medication used may include aripiprazole monohydrate.

干预措施: Standard of care long acting injectable medication for bipolar disorder (Other)

Oral medication + ketogenic diet

Experimental

Participants in this arm will receive oral medication for bipolar disorder, plus foodstuffs necessary to support ketogenic diet. Oral medications may include second generation antipsychotic mood stabilizing medications aripiprazole, risperidone, quetiapine, and olanzapine.

干预措施: Ketogenic foodstuffs (Dietary Supplement)

Oral medication + ketogenic diet

Experimental

Participants in this arm will receive oral medication for bipolar disorder, plus foodstuffs necessary to support ketogenic diet. Oral medications may include second generation antipsychotic mood stabilizing medications aripiprazole, risperidone, quetiapine, and olanzapine.

干预措施: Standard of Care Oral antipsychotics (Other)

Oral bipolar medication only

Active Comparator

Participants in this arm will receive oral medication treatment as usual for bipolar disorder. These medications may include second generation antipsychotic mood stabilizing medications aripiprazole, risperidone, quetiapine, and olanzapine.

干预措施: Standard of Care Oral antipsychotics (Other)

Long-acting injectable medication only

Active Comparator

Participants in this arm will receive long-acting injectable medication as treatment for bipolar disorder. This medication may include aripiprazole monohydrate.

干预措施: Standard of care long acting injectable medication for bipolar disorder (Other)

Long-acting injectable medication + ketogenic diet

Experimental

Participants in this arm will receive long-acting injectable medication for bipolar disorder, plus foodstuffs necessary to support ketogenic diet. The medication used may include aripiprazole monohydrate.

干预措施: Ketogenic foodstuffs (Dietary Supplement)

结局指标

主要结局

Impact on Symptom Severity as measured by Young Mania Ratings Scale

时间窗: T0 (time of intake); T0+1 week; T0+2 weeks; T0+3 weeks; T0+4 weeks; T0+6 weeks; T0+8 weeks; T0+10 weeks; T0+12 weeks; T0+16 weeks; T0+20 weeks; T0+24 weeks

The Young Mania Rating Scale (YMRS) is a clinical assessment tool specifically designed to evaluate manic symptoms and their severity. The YMRS comprises 11 items. Each item is rated on a scale that varies in range, typically from 0 to 4 or 0 to 8, allowing for a nuanced measurement of symptoms. The total score can range from 0 to 60, with higher scores indicating more severe manic symptoms.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Will Rutland

Regional Chair of Psychiatry - Montgomery Campus

University of Alabama at Birmingham

研究点 (1)

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