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临床试验/NCT07308483
NCT07308483尚未招募不适用

Ketogenic Approach to Restore Muscle in Older Patients With Community-Acquired Pneumonia - KARMA-P Trial

University of Alabama at Birmingham1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2026年10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
30
试验地点
1
主要终点
Adherence to the Intervention

研究概览

简要总结

The purpose of the study is to see if a ketogenic diet compared to a standard diet is better to maintain muscle function and health in hospital admitted pneumonia patients.

详细描述

Bacterial community-acquired pneumonia (CAP) is a leading cause of hospitalization and mortality in older adults, often resulting in significant muscle wasting, systemic inflammation, and microbiome dysbiosis. Muscle loss, driven by bedrest, acute illness, and antibiotic-induced dysbiosis, all contribute to prolonged hospital stay, delayed recovery, and long-term physical decline. Current interventions such as physical rehabilitation and increased protein intake are largely ineffective in mitigating the acute illness-induced muscle wasting due to metabolic dysfunction such as impaired glucose control. Preliminary evidence suggests that ketogenic enteral feeding is safe, reduces inflammation, stabilizes metabolism and preserves functional outcomes in hospitalized patients. Because most of older hospitalized CAP patients are able to ingest food orally, our study aims to test the safety, feasibility and determine effect sizes for preliminary evidence of a 10-day oral ketogenic diet (low carbohydrate, high fat) in older CAP patients.

The investigators will conduct a double-blinded pilot randomized clinical trial in 30 hospitalized older adults (>55 years) with bacterial CAP, randomizing participants to a ketogenic feeding (n=15) or standard hospital feeding (n=15). Muscle mass will be assessed using ultrasound, inflammatory and metabolic biomarkers from blood, and microbiome composition from oral and skin swabs collected at baseline, 10-Day post-intervention, and 1-month post-intervention follow-up. Handgrip strength will be collected at baseline and 10-day follow-up. Physical activity measures (accelerometry) will be measured for 7 days after the 10-day and 1-month follow-up visits. Physical function (short physical performance battery), handgrip strength, and activity levels (accelerometry) will be measured at 1-month follow-up. Daily blood ketone level measurements will guide feeding adjustments to maintain ketosis, and dietary habits will be assessed weekly post-intervention until 1-month follow-up. Meals for the 10-day intervention will be prepared in a metabolic kitchen by a clinical nutritionist.

If successful, this study will provide evidence for oral ketogenic feeding as an innovative intervention to prevent muscle wasting and functional decline, supporting a future phase IIb clinical trial targeting middle-aged and older adults hospitalized with CAP.

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
Double (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • Age 55 years and older
  • Bacterial community-acquired pneumonia
  • Expected at least 10-day stay in the hospital
  • Ability to ingest food orally
  • Willingness to be randomized to either treatment group
  • Willingness to participate in all study procedures

排除标准

  • Failure to provide informed consent
  • Vegetarian/vegan
  • Severe cardiac disease, including NYHA Class III or IV congestive heart failure, clinically significant aortic stenosis, history of cardiac arrest, use of a cardiac defibrillator, or uncontrolled angina
  • Diagnosed dementia
  • Hip fracture, hip or knee replacement, or spinal surgery within past 4 months
  • Simultaneous participation in another intervention trial

研究组 & 干预措施

ketogenic feeding

Active Comparator

The ketogenic feeding will have a macronutrient composition of approximately 10% energy from carbohydrates, 25% energy from protein, and 65% energy from fat.

干预措施: Ketogenic feeding (Behavioral)

Standard feeding

Placebo Comparator

The standard, control diet will be compatible with the USDA guidelines. It will consist of approximately 60% carbohydrate, 20% protein, 20% fat. Participants will be given low-fat foods, whole-grain foods, fruits, and vegetables.

干预措施: Standard feeding (Behavioral)

结局指标

主要结局

Adherence to the Intervention

时间窗: From baseline to 1 month follow-up

Percentage of prescribed intervention sessions completed, assessed through adherence logs and system usage records (Unit: %)

Incidence of Adverse Events

时间窗: At baseline, at 10-day of feeding, and at 1 month follow-up

Number of adverse events collected using a standardized adverse event reporting form (Unit: Count of events).

次要结局

  • Handgrip strength(At baseline, 10-Day post-intervention, and 1-month post-intervention follow-up)

研究者

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

Robert T Mankowski

Associate Professor

University of Alabama at Birmingham

研究点 (1)

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