跳至主要内容
临床试验/NCT03073811
NCT03073811已完成不适用

Nutritional (High Protein) Perihabilitation in Older Veterans Undergoing Surgery

VA Office of Research and Development1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2017年6月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
1
主要终点
Determine Acceptability of Perioperative Protein-enhanced Intervention Compared to an Educational Control

研究概览

简要总结

This research study will be conducted in two parts. The first part will consist of selecting appropriate screening and assessment tools for Veterans undergoing elective surgery and identifying the number of Veterans who are malnourished and at risk of malnutrition. The second portion of the study will be to determine if a protein-enhanced diet before and after surgery will improve function and postoperative outcomes and compare the results to an education control group.

详细描述

In year 1 of the two-part research study, an observational, prospective study of 75 Veterans preparing for elective surgery will be conducted. The purpose of this study will be to select appropriate nutrition screening and assessment tools and to employ them to characterize malnutrition prevalence and severity and establish cut-off values associated with malnutrition in this population. In years 2-5 of the research two-part research study, a pilot randomized controlled trial will be conducted. The purpose of this study will be evaluate the feasibility, fidelity, and acceptability of a perioperative protein-enhanced intervention compared to an educational control. Veterans who are malnourished or at risk of being malnourished will be randomly assigned on a 1:1 ratio to either an education (nutritional counseling) control or high-protein perihabilitation arm. Participants in the high-protein perihabilitation arm will be provided with 30 grams of high quality protein supplements three times per day. The study will take place two weeks prior to an elective abdominal or GI surgery and will continue 4 weeks post surgery.

研究设计

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

入排标准

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

入选标准

  • •Elective abdominal surgery
  • •colorectal
  • •hepatobiliary
  • •pancreatic
  • •intra-abdominal
  • •Abdominal aortic aneurysm
  • •Referred to the VA Perioperative Optimization of Senior Health Clinic
  • •Able to record dietary intake or has a proxy who can record dietary intake

排除标准

  • •Cognitive impairment
  • •Unwillingness to be randomized to either intervention arm, submit to study testing, or continuously participate in the intervention for six weeks
  • •Living in skilled nursing facility
  • •No access to telephone

研究组 & 干预措施

PeriHab

Experimental

Provided nutrition counseling and prescribed to consume 1.6 g/kg/body weight as well as provided 30 grams of high quality protein three times per day for two weeks before and four weeks after surgery.

干预措施: Protein enhanced nutrition intervention (Dietary Supplement)

PoshControl

Active Comparator

Provided nutrition counseling and prescribed to consume 1.0 g/kg/body weight in the form of educational handouts explained by a Registered Dietitian and one oral nutrition supplement per day for two weeks before surgery.

干预措施: Education Control (Other)

结局指标

主要结局

Determine Acceptability of Perioperative Protein-enhanced Intervention Compared to an Educational Control

时间窗: 30-day post-surgery follow-up (endpoint)

Satisfaction of overall participation in the research study (Likert Scale). I am glad I participated in this research study. 1 - Strongly Disagree and 5- Strongly Agree

Physical Function

时间窗: Baseline, day of surgery (an average of 12 days from baseline), 30-days post-surgery

Short physical performance battery - higher scores means a better physical performance (Total score = 0-12)

Evaluate the Feasibility of a Perioperative Protein-enhanced Intervention Compared to Control Arm.

时间窗: day of surgery (an average of 12 days from baseline [midpoint]) and 30-day post-surgery (endpoint)

Feasibility was measured as retention. Hypothesis was that 80% of the participants would be retained.

次要结局

未报告次要终点

研究者

申办方类型
Fed
责任方
Sponsor

研究点 (1)

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