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临床试验/NCT04923672
NCT04923672终止不适用

Evaluation of the Feasibility of Wearable Technology-Guided Exercise Preconditioning to Accelerate Return to Function After Cancer Surgery

University of Virginia2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2023年2月20日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
10
试验地点
2
主要终点
Steps per day

研究概览

简要总结

Studies have shown that people who are more physically fit prior to surgery do better after surgery. For this reason, it may be helpful for people who are going to have abdominal surgery for cancer to exercise before surgery to increase fitness. In this study, patients will be assigned to either maintain their current activity, or increase activity to 5 days a week, 40 minutes per day, of either continuous moderate activity or intervals of moderate and vigorous activity (three groups). All participants will wear an Apple watch, and participants in the exercise groups will use a smartphone application to get feedback on activity and encouragement to reach activity goals.

详细描述

Research indicates that people who have better physical fitness at the time of surgery have a better chance of surviving the surgery and returning to normal function. An exercise intervention in the 3+ weeks before surgery (after the decision that surgery is necessary) may help people who are going to have abdominal surgery for cancer increase fitness prior to surgery. Devices that track physical activity, like smartwatches or Fitbits, allow the wearer to get feedback on physical activity information like steps taken, distance traveled, time in light, moderate or vigorous activity and on heart rate. Having this information and using a smartphone application designed to increase physical activity may help patients increase physical activity and thereby fitness, prior to abdominal surgery for cancer.

The main goal of this project is to test two physical activity interventions and also a "control group" to make sure that participants can do the interventions and to see whether there are changes in activity and fitness in each group:

  1. Control group - maintain current activity
  2. Moderate continuous activity group - increase activity to 5 days a week, 40 minutes per day, of continuous moderate activity
  3. High Intensity Interval Training group - increase activity to 5 days a week, 40 minutes per day, of intervals of moderate and vigorous activity

All participants will wear an Apple watch, and participants in the exercise groups will use a smartphone application to get feedback on activity and encouragement to reach activity goals.

Optional: Participants will also be asked to provide a small amount of blood for research purposes.

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

  • Adult (≥ 18 years of age) patients undergoing elective abdominal oncologic resection of a confirmed or potential colorectal, hepatobiliary, or gynecologic neoplasm.
  • Study participants must be able to provide written informed consent and authorization.
  • Study participants must be able to understand written and verbal English, as well as to be able to communicate in English.
  • Study participants must have an Apple iphone to use during the study period

排除标准

  • Any patient unable and/or unwilling to cooperate with all study protocols.
  • Patients who require an assist device (walker) for ambulation.
  • Patients that indicate they did at least 3 days of vigorous intensity activity in the previous 7 days OR any combination of walking, moderate-intensity or vigorous-intensity in all of the last 7 days totaling at least 18 and a half hours
  • Recent history of cardiac disease (within 3 months of registration) that would preclude vigorous exercise
  • Individuals with end stage renal disease currently on dialysis
  • Individuals with a history of liver failure as evidenced by AST, ALT or Alkaline Phosphatase ≥ 3x upper limit of normal
  • Individuals with uncontrolled hypertension
  • Women who are breastfeeding or pregnant
  • American Society of Anesthesiologists Physical Status score ≥ 4
  • Any patient that needs further cardiac evaluation per ACC/AHA perioperative criteria
  • Surgery scheduled < 3 weeks of study registration (precluding time to participate in exercise regimen)
  • Any patient who currently uses a fitness tracker or heart rate monitoring-capable device to guide exercise
  • Patient indicates a lack of familiarity or discomfort with using a smartphone
  • If participation is not in the best interest of the patient, in the opinion of the treating investigator

结局指标

主要结局

Steps per day

时间窗: Baseline through the 1 day visit prior to surgery

Change in average steps per day measured at baseline and at the time of surgery

次要结局

  • Surgical complications(30 days after surgery)
  • Compliance with exercise intervention, including percentage of exercise goals reached(From baseline through 1 day visit just prior to surgery)
  • Completion/Dropout rate(From baseline through about 30 days after surgery)
  • Enrollment rate(During participant accrual, estimated to take about 12 months)
  • Percentage of time wearing Apple Watch(From baseline through about 30 days after surgery)
  • Pain interference(Baseline and 1 day of surgery)
  • Physical activity level by self report(Baseline and 1 day of surgery)
  • Steps per day(From baseline through 30 days after surgery)
  • Compliance with EXi smartphone application(From baseline through 1 day visit just prior to surgery)
  • Health-related quality of life(Baseline and 1 day of surgery)
  • Pain intensity(Baseline and 1 day of surgery)
  • Length of hospital stay (in days) following surgery(Up to 30 days following surgery)
  • Fitness level(Baseline, 1 day prior to surgery, and 30, 90, and 180 days following surgery)

研究者

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

Traci Hedrick, MD

Associate Professor

University of Virginia

研究点 (2)

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