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临床试验/NCT07417891
NCT07417891尚未招募不适用

Ketogenic Diet to Reduce Osteoarthritis Pain in MCI

University of Kansas Medical Center1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2026年6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
10
试验地点
1
主要终点
Pain intensity and pain interference using a Visual Analog Scale

研究概览

简要总结

Osteoarthritis and mild cognitive impairment are common conditions that share underlying biological processes related to metabolism and inflammation. This study will examine whether a well-formulated ketogenic diet influences pain, physical function, and cognitive outcomes in adults with osteoarthritis and mild cognitive impairment. Participants will follow a supervised ketogenic dietary intervention, with assessments conducted before and after the intervention to evaluate changes in symptoms and related biological markers. The goal of this study is to better understand shared mechanisms between joint pain and cognitive health and to explore whether a ketogenic dietary approach may support symptom management in these populations.

详细描述

OA and dementia are two leading contributors to disability worldwide. Although traditionally studied separately, accumulating evidence indicates substantial overlap in their underlying inflammatory, metabolic, and neuroimmune pathways. Chronic OA pain is associated with systemic inflammatory mediators, increased peripheral nociceptor sensitization, impaired descending inhibition, and central neuroinflammation driven by microglia and astrocyte activation. These same mechanisms contribute to cognitive decline, reduced synaptic plasticity, hippocampal vulnerability, and progression from MCI to ADRD.

In aging adults, chronic pain accelerates cognitive decline and increases risk for dementia, and cognitive impairment exacerbates pain-related disability. Neuroinflammation-particularly microglial activation and NLRP3 inflammasome signaling-is a shared mechanistic link between the two conditions. Identifying interventions that target this shared biology is crucial for improving outcomes for older adults with comorbid pain and cognitive decline.

The ketogenic diet has demonstrated therapeutic effects in multiple neurological, metabolic, and inflammatory conditions. Mechanisms include suppression of the NLRP3 inflammasome, improved mitochondrial efficiency, enhanced lipid metabolism via TREM2-associated pathways, reduced oxidative stress, reduced systemic inflammation, glycemic control, and modulation of gut microbiota.

Preclinical data show that ketone bodies improve cognitive function and reduce neuroinflammation in models of AD. Human studies demonstrate the feasibility and potential cognitive benefit of WFKD in ADRD populations and post-concussion syndrome. Additionally, this study team recently investigated the impact of an 8-week WFKD on modifiable risk factors associated with metabolic syndrome, on gut microbiota structure, and RNASeq in healthy, middle-aged adults. However, the application of a WFKD to individuals with OA and early cognitive impairment is unexplored. Our team has conducted two previous clinical trials and is currently analyzing outcomes of an NIA-funded clinical trial using the WFKD. Participants from these trials have successfully adopted the WFKD, evidenced by objective and reported ketone body production and macronutrient profile of dietary intake. The WFKD used in these trials improved micronutrient intake and intake of non-starchy vegetables, and suggests that the WFKD may benefit cognition in patients with AD and symptoms in patients with post-concussion syndrome.

This population is particularly relevant given the aging US population, the high prevalence of OA-associated chronic pain, the presence of early neuroinflammation and neurodegeneration, poor diet quality contributing to systemic inflammation, and heightened vulnerability to cognitive decline, reduced quality of life, and hospitalization/institutionalization.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
55 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • English speaking
  • Diagnosis of major joint osteoarthritis
  • Diagnosis of mild cognitive impairment

排除标准

  • Diabetes that requires insulin
  • Cancer requiring chemo- or radiation therapy in the last 2 years
  • Cardiac event within 1 year
  • Recent history of renal stones
  • Diagnosis of fibromyalgia
  • Already following a ketogenic diet
  • Following a dietary pattern that does not allow for a ketogenic approach
  • Unable to control one's diet

研究组 & 干预措施

Well-formulated ketogenic diet

Experimental

This is a dietary intervention that is very low carbohydrate, higher healthy fats, and adequate protein.

干预措施: Well-formulated ketogenic diet (Other)

结局指标

主要结局

Pain intensity and pain interference using a Visual Analog Scale

时间窗: From enrollment to the end of treatment at 8 weeks

Patient- and caregiver-reported outcome. 0-10 with higher scores reflecting worse pain.

Health-related quality of life using a Questionnaire

时间窗: From enrollment to end of treatment at 8 weeks

Patient- and caregiver-reported ouctome.The PROMIS-29+2 Profile is a patient-reported outcome measure with domain scores converted to standardized T-scores (mean = 50, SD = 10), where higher scores indicate worse symptoms for anxiety, depression, fatigue, sleep disturbance, and pain interference, better functioning for physical function, social participation, and cognitive function, and pain intensity is rated separately on a 0-10 scale with higher scores indicating greater pain.

Physical Function via Functional Activities Questionnaire

时间窗: From enrollment to end of treatment at 8 weeks.

Caregiver-reported outcome. FAQ is 0-30 with higher scores indicating worse impairment.

Montreal Cognitive Assessment (MoCA) for brief global cognitive screening

时间窗: From enrollment to end of treatment at 8 weeks.

Cognitive screener completed by the participant and administered by the study coordinator. The Montreal Cognitive Assessment (MoCA) is a 30-point cognitive screening tool assessing multiple cognitive domains, with total scores ranging from 0 to 30 and higher scores indicating better cognitive function.

次要结局

  • Central sensitization(From enrollment to end of treatment at 8 weeks.)
  • Ketone levels(From enrollment to end of treatment at 8 weeks.)

研究者

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

Doug Wright

Professor and Vice Chair of Research, Department of Anesthesiology

University of Kansas Medical Center

研究点 (1)

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