跳至主要内容
临床试验/NCT02531620
NCT02531620Unknown不适用

Prehabilitation Interventions in Elective Colorectal Resections: A Randomized Pilot Study (Prehab)

McMaster University2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2015年9月最近更新:
适应症

试验速览

阶段
不适用
入组人数
70
试验地点
2
主要终点
Number of participants recruiting

研究概览

简要总结

This is a pilot study designed to evaluate a programme of rehabilitation for patients undergoing elective colorectal resection surgery.

详细描述

Operations on the colon and rectum are major abdominal operations and many individuals can become severely deconditioned or weakened afterwards. For some individuals this can even mean that they can no longer completely return to their usual way of life following one of these major operations. As part of this study the investigators are attempting to identify ways to maximize patients' recovery and to maximize their overall quality of life following these major operations. It is possible that preconditioning may make a difference to patient's overall quality of life, decreased or need for hospital length of stay and decreased postoperative medical complications occasionally seen during these operations, in essence provide an overall enhancement to their surgical recovery. Physiatrists are physicians who are medical experts in maximizing a patient's overall ability to function well and live independently. Investigators are proposing patient participation in an initial pilot study in order to test the question as to whether or not participation with a physiatrist and any interventions recommended by said physician would help improve a patient's postoperative recovery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
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 patient
  • scheduled to undergo a colorectal resection as part of treatment for colorectal cancer.
  • English speaking or have available a family member or substitute decision maker who can accompany you to all of your study visits.

排除标准

  • geographic inaccessibility
  • unwilling to provide consent

结局指标

主要结局

Number of participants recruiting

时间窗: 6 months

Screening and recruiting of eligible patients

次要结局

  • Mortality(6 months)
  • Length of Stay(30 days post-op)
  • Number of patients with readmissions(30 days and 6 months)
  • Functional Independence Assessment (UK Functional Independence Measure and Functional Assessment Measure)(1, 3 and 6 months)
  • Quality of Life Survey (Short Form 36 Health Survey)(1, 3 and 6 months)
  • Bowel Function Assessment(1, 3 and 6 months)
  • Post-op complications(30 days)
  • Physical Function Assessment (6 Minute Walk Test)(1, 3 and 6 months)
  • Pain Assessment (Visual Analog Scale)(1, 3 and 6 months)
  • Symptom Assessment (Edmonton Symptom Assessment System)(1, 3 and 6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验