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Trial record 3 of 1534 for:    Enhancing Outcomes

Enhancing Outcomes After Colon Surgery

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00227526
Recruitment Status : Completed
First Posted : September 28, 2005
Last Update Posted : September 6, 2010
Canadian Anesthesiologists' Society
Information provided by:
McGill University

Brief Summary:
Most patients find that recovering from surgery is difficult particularly after abdominal surgery for cancer or other intestinal disorders. The surgical stress, healing process and concerns if further treatments are required suggest that the post-operative period may not be the best time to get people to exercise to rehabilitate lost functions. Prehabilitation is the process of enhancing functional capacity of the individual to enable him or her to withstand an incoming stressor, such as surgery, and this study aims to evaluate the effectiveness of prehabilitation for colorectal surgery. Two groups will be formed by a random process and the prehabilitation group will use an exercise cycle and weights to build endurance and strength for a 3-week period prior to surgery. The other group will receive training about exercises that will help them move better after surgery. People who are malnourished prior to surgery will receive nutritional supplements. The results of this trial will be used to inform practitioners and patients alike of the benefits (or risks if any) of exercise in preparing for surgery.

Condition or disease Intervention/treatment Phase
Colorectal Surgery Behavioral: Prehabilitation Phase 2

Detailed Description:

The surgical process is a major stressor because of the psychological distress, tissue trauma, lack of activity, and quasi-starvation and it produces immediate systemic changes and both short- and long-term effects on activity and quality of life. However, there is mounting evidence that many of the negative immediate effects of surgery such as pain, fatigue, and weakness are amenable to intervention. If proper interventions are carried out, these symptoms may be readily controlled allowing for a faster recovery and early home discharge. But the effects of surgery are felt far beyond the immediate convalescent period and patients can feel fatigued for many weeks and this delays return to usual function and reduces quality of life. Thus, it would be of great practical benefit if ways of improving post-surgery physical function and quality of life could be identified.

Traditionally efforts have been made to improve the recovery process by intervening in the post-operative period. However, the post-operative period may not be the most opportune time to introduce interventions to accelerate recovery. Many of these surgical patients are concerned about perturbing the healing process as well as being depressed and anxious if they await further treatment. The pre-operative period may be a more emotionally salient time to intervene in the factors that contribute to recovery. The process of enhancing functional capacity of the individual to enable him or her to withstand an incoming stressor has been termed prehabilitation The purpose of this study is to address the following research question: Among persons scheduled for colorectal surgery, does a pre-operative program of aerobic and muscle strength training (prehabilitation) compared to a standard peri-operative educational protocol affect functional exercise capacity and health-related quality of life? The trial will be a single blind, stratified (on cancer diagnosis or not), randomized, two-group (prehabilitation or standard care), parallel design. Both groups will receive the same peri-operative education program. In conformity with current practice, all subjects will also be advised on nutritional support during the preoperative period. Persons with albumin < 38 gm./l will receive an adequate supply of protein and calorie nutritional supplement bars. In addition to this standard care, the prehabilitation group will be prescribed a program of exercise training consisting of daily stationary cycling from the start of the intervention to the day prior to surgery (minimum 3 weeks) combined with an individualized program of muscle strength training.

Both groups will be evaluated for exercise tolerance, walking capacity and health and emotional status at enrolment and after 3 three weeks of training as well as at 4 weeks, 8 weeks and 24 weeks (6 months) post-surgery. The main outcome measure will be the 6 Minute Walk Test - a valid and reliable measure of functional walking capacity. The estimator of effect will be the proportion of people in each group who, at 8 weeks post-surgery, achieve or exceed their baseline value on this test (± 20m). The proposed sample size is 200. This is based on 80% power to detect a difference of 22% in the proportion recovering to baseline values (40% in standard and 62% in prehabilitation). The results of this trial will be used to inform practitioners and patients alike of the benefits (or risks if any) of exercise in preparing for surgery.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 200 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Outcomes Assessor)
Primary Purpose: Prevention
Official Title: Enhancing Outcomes After Colon Surgery: Role of Prehabilitation Facilitating the Recovery Process.
Study Start Date : February 2005
Actual Primary Completion Date : December 2008
Actual Study Completion Date : December 2008

Primary Outcome Measures :
  1. 6 Minute Walk Test [ Time Frame: baseline, 3 weeks, 4 weeks, 8 weeks, 24 weeks ]

Secondary Outcome Measures :
  1. V02 max and submax [ Time Frame: baseline, 24 weeks ]
  2. SF-36 - Short form 36 [ Time Frame: baseline, 3 weeks, 4 weeks, 8 weeks, 24 weeks ]
  3. CHAMPS - Community Healthy Activities Model Program for Seniors [ Time Frame: baseline, 3 weeks, 4 weeks, 8 weeks, 24 weeks ]
  4. Hospital Anxiety Depression Scale - HADS [ Time Frame: baseline, 3 weeks, 4 weeks, 8 weeks, 24 weeks ]
  5. Fatigue and Pain VAS [ Time Frame: baseline, 3 weeks, 4 weeks, 8 weeks, 24 weeks ]
  6. Visual Analogue Mood States (VAMS) [ Time Frame: baseline, 3 weeks, 4 weeks, 8 weeks, 24 weeks ]
  7. 2Minute Walk Test [ Time Frame: baseline, 3 weeks, 4 weeks, 8 weeks, 24 weeks ]
  8. Complications: infection (wound, sepsis, urinary, lung); bleeding; wound dehiscence; technical complications (ileus, anastomotic leakage); stroke, MI, DVT/PE, delirium, fall w/wo injury; malnutrition; urinary retention; respiratory failure [ Time Frame: baseline, 3 weeks, 4 weeks, 8 weeks, 24 weeks ]
  9. Charges for bed day: surgical procedure; surgeon/anaesthesiologist; pre, post and follow-up tests and procedures; visits; follow-up medications [ Time Frame: baseline, 3 weeks, 4 weeks, 8 weeks, 24 weeks ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Age 18 and above
  • Referred electively for colorectal resection for benign (polyposis adenoma diverticulitis) or non-disseminated colon and rectum cancers
  • Referred electively for colorectal resection for colon reconstruction for non-active inflammatory bowel disease
  • Referred electively for colorectal resection for fibrostenotic conditions that are a feature of Crohn's disease.

Exclusion Criteria:

  • People with American Society of Anesthesiologists health status class 4-5
  • Co-morbid medical conditions interfering with the ability to participate in either group or complete the testing procedures (e.g. dementia, disabling orthopedic and neuromuscular disease, psychosis)
  • Patients at high risk for a cardiac complication during exercise at home: severe aortic stenosis, cardiac failure Class IV NYHA, myocardial infarction within 6 months, congestive heart failure, and unstable angina
  • Persons with sepsis; and treatment with chemotherapy or radiotherapy during six months prior to the date of surgery
  • Those with very low exercise tolerance (<3.5 METS) as determined by the baseline exercise test
  • Anyone with a cardiac arrhythmia that manifests during the baseline exercise testing, prior to randomization
  • Those people who are already in excellent physical condition owing to a regular participation in a high intensity physical activity. On testing, persons whose age-predicted value on the 6MWT exceeds 130% will be excluded (expected <10%)

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00227526

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Canada, Quebec
Montreal General Hospital
Montreal, Quebec, Canada, H3G 1A4
Sponsors and Collaborators
McGill University
Canadian Anesthesiologists' Society
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Principal Investigator: Francesco Carli, MD McGill University Health Centre/Research Institute of the McGill University Health Centre
Principal Investigator: Nancy Mayo, PhD McGill University
Publications automatically indexed to this study by Identifier (NCT Number):
Layout table for additonal information Identifier: NCT00227526    
Other Study ID Numbers: REC02-053
First Posted: September 28, 2005    Key Record Dates
Last Update Posted: September 6, 2010
Last Verified: September 2010
Keywords provided by McGill University: