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临床试验/NCT03357497
NCT03357497已完成不适用

Very Early Mobilization of Colorectal Surgery Patients - A Randomized Controlled Trial

Region Örebro County2 个研究点 分布在 1 个国家目标入组 146 人开始时间: 2017年9月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
146
试验地点
2
主要终点
Physical activity level measured with accelerometry

研究概览

简要总结

Early mobilization is an important part of Enhanced Recovery Programs (ERP)in colorectal surgery. The aim of this randomized controlled trial is to investigate the impact of very early mobilization, starting within 1 hour after surgery, on further mobilization within an existing Enhanced Recovery Program.

详细描述

Post-operative bed rest and immobility has a negative effect on morbidity and mortality after colorectal surgery.To prevent immobilization early mobilization is a well established part of Enhanced Recovery Programs. This facility uses protocols developed by the ERAS (Enhanced Recovery After Surgery)-society. However not all patients can reach the level physical activity needed to be in compliance with the ERP. This being more frequent in the elderly frail patient. This may contribute to longer hospital stay and increase the risk of complications. The aim of this trial is to investigate if a very early mobilization intervention will lead to a higher lever of physical activity after surgery compared with standard-care.

The aim is to include 150 patients scheduled to undergo colorectal surgery. Patients will receive written and verbal information about the trial before written consent is obtained. The patients will undergo an extended pre-operative assessment during which a baseline for patients physical activity level will be established before surgery. For this purpose the patients will be evaluated by a physiotherapist with the following tools; 6-minutes walk test, Timed up and go-test (TUG), mini modified Functional Independence Measure (mFIM), WHO disability assessment score (WHODAS) and activity measurement with accelerometry for up to 7 days. (Actigraph GT3X device)

The randomization will take place on the day of the surgery and the patients will be assigned to either intervention (very early mobilization) or control group (standard post-operative care). A stratified randomization will be performed to ensure an even spread within three patient categories: Laparoscopic surgery, Open surgery and Rectum amputation. The randomization is performed using concealed allocation where envelopes are prepared externally using a randomization list prepared by a statistician.

After surgery the patients will be transferred to the post-operative care unit where the patients included in the intervention group will be mobilized with the help of a physiotherapist and post-operative unit staff. The intervention will begin as early as 30 minutes after arrival in the post-operative unit. The intervention will follow the Surgical ICU Optimal Mobilization Score (SOMS) which includes four steps of mobilization from movement in bed up to walking. Progress from each step to the next will be conditioned with patient fulfilling criteria for a safe mobilization including stable physiological parameters and adequate pain situation. The patients in the standard care group will not receive the intervention.

All patients will receive information about early mobilization. The patients will not receive information on the timing of the mobilization intervention in an effort to remain blinded to the intervention. The patient in the standard care group will be mobilized accordingly to the ERP protocol, which also includes early mobilization in the surgical ward. Upon transfer from the post-operative unit to the surgical ward all study patients will be again fitted with the activity monitor to measure their physical activity during the post-operative phase.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • All patients over the age of 18 scheduled for colorectal surgery

排除标准

  • Unable to understand study information (language,cognitive impairment, etc.)
  • Unable to walk

结局指标

主要结局

Physical activity level measured with accelerometry

时间窗: 72 hours

Comparison between intervention and standard-care group by measurements of physical activity level with an accelerometer that the patient wears during the day. The accelerometer is worn at hip level.

次要结局

  • Pulse during the SOMS intervention.(one day)
  • Presence of vertigo(one day)
  • Severity of post-operative complications(one year)
  • Time out of bed measured with a protocol(7 days)
  • Minutes in the postoperative ward(one year)
  • Days in the hospital ward(one year)
  • Number of adverse events during the SOMS intervention.(one day)
  • Blood pressure during the SOMS intervention.(one day)
  • Oxygen saturation during the SOMS intervention.(one day)
  • Pain(one day)
  • Presence of nausea(one day)
  • 6 minute Walking test(6 weeks)
  • Timed up and Go (TUG) test(6 weeks)
  • Patient perception of the SOMS intervention(6 weeks)
  • Self-perceived health and physical function level one year after surgery(one year)

研究者

发起方
Region Örebro County
申办方类型
Other
责任方
Sponsor

研究点 (2)

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