跳至主要内容
临床试验/NCT03094988
NCT03094988已完成不适用

COgnitive and Physical Exercise (COPE) Prehabilitation to Improve Outcomes in Surgical Patients: A Pilot Feasibility Study

Vanderbilt University2 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2017年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
32
试验地点
2
主要终点
Participation log and diary

研究概览

简要总结

Cognitive and functional impairment are debilitating problems for survivors of major surgery. Efforts to modify medical treatments to prevent such impairment are ongoing and may yet yield significant benefits. An area in need of study is whether building patients' cognitive and physical reserve through a prescribed program of cognitive and physical exercise before the physiological insult (a prehabilitation effort) can improve long-term outcomes. Prehabilitation efforts before surgery thus far have focused on preemptive physical therapy to improve post-surgical functional outcomes. No work, however, has been done to attenuate the cognitive decline commonly seen after surgical illness by exercising the brain before the surgical insult. Cognitive prehabilitation is a novel therapeutic approach that applies well-understood techniques derived from brain plasticity research. Our approach is bolstered by data that demonstrate that cognitive training programs are effective and have a very high likelihood of fostering improvement in patient outcomes across a range of populations. It is not yet known if these programs can improve cognitive reserve, allowing patients' minds to better manage the acute stress of surgery and hospitalization. The primary aim of this pilot study is to evaluate the feasibility of cognitive and physical prehabilitation training in adult patients undergoing major non-cardiac surgery who are at risk for postoperative cognitive and functional decline. The secondary aim is to study the effects of cognitive and physical prehabilitation training on cognitive abilities, functional status, and quality of life after surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
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

  • Adults undergoing major surgery with the likelihood of prolonged hospitalization or critical illness among the following surgical services: general surgery, surgical oncology, otolaryngology, hepatobiliary, thoracic, and vascular surgery

排除标准

  • Blind, deaf, or unable to speak English, as these conditions would preclude our ability to perform the proposed cognitive and physical program
  • Pregnancy
  • Prisoners
  • Severe frailty or physical impairment that prohibits participation in prehabilitation program
  • Patients with documented dementia or cognitive impairment that precludes ability to self-consent for surgery and study participation
  • Less than 2 weeks from scheduled surgery
  • Patients without home internet access

结局指标

主要结局

Participation log and diary

时间窗: From date of randomization to surgery, approximately 4 weeks

Proportion of eligible days that patients performed the cognitive and physical prehabilitation program, duration of time per day patients spent on each program

次要结局

  • Instrumental activities of daily living(Approximately 1 month after surgery at the post-surgical clinic follow-up)
  • Hospital length of stay(From time of surgery until time of discharge or death, whichever came first, assessed up to 30 days)
  • Activities of daily living(Approximately 1 month after surgery at the post-surgical clinic follow-up)
  • Cognitive assessment(Approximately 1 month after surgery at the post-surgical clinic follow-up)
  • Discharge location(From time of surgery until time of discharge or death, whichever came first, assessed up to 30 days)
  • Muscle strength(Approximately 1 month after surgery at the post-surgical clinic follow-up)
  • Functional exercise capacity(Approximately 1 month after surgery at the post-surgical clinic follow-up)
  • Pulmonary function(Approximately 1 month after surgery at the post-surgical clinic follow-up)
  • Acute brain dysfunction(During hospital stay after surgery, for up to 2 weeks)
  • Pain levels(During hospital stay, for up to 2 weeks, and approximately 1 month after surgery at the post-surgical clinic follow-up)

研究者

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

Christopher Hughes

Associate Professor of Anesthesiology

Vanderbilt University

研究点 (2)

Loading locations...

相似试验