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Prehabilitation in Colorectal Cancer

Primary Purpose

Colon Cancer

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Prehabilitation
Rehabilitation
Sponsored by
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colon Cancer

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of colon cancer requiring surgery;
  • more than 40 years of age;
  • autonomous and voluntary person;
  • able to read, write and understand French;
  • Frailty phenotype criteria < 3

Exclusion Criteria:

  • a physical impairment that would seriously impair physical mobility;
  • an unfavorable familial context;
  • a stoma;
  • American Society of Anesthesiologists score IV-V;
  • emergency;
  • neuropsychiatric disease.

Sites / Locations

  • Cliniques universitaires Saint-Luc

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Prehabilitation group

Rehabilitation group

Arm Description

Preoperative and postoperative telerehabilitation

Postoperative telerehabilitation

Outcomes

Primary Outcome Measures

Change in cardiorespiratory fitness
Cardiorespiratory is measured by a 6-minute walk test

Secondary Outcome Measures

Change in muscle strength
Muscle strength is measured by using an isokinetic dynamometer
Change in muscle endurance
Muscle endurance is measured by using the "1-minute sit-to-stand-test" (number of sit-to-stand cycles during 1 minute)
Change in quality of life
Quality of life is measured by using the Euroquol-5D-3L questionnaire
Change in fatigue
Fatigue is measured by using the Functional Assessment of Cancer Therapy: Fatigue questionnaire
Change in level of physical activity
Level of physical activity is measured by using the International Physical Activity Questionnaire Short Form
Change in executive functions
Executive functions is measured by using the Trail Making test
Change in executive functions
Executive functions is measured by using the Fluency test
Change in weight
Weight (kg) is measured by using a bioelectrical impedance analysis
Change in lean body mass
Lean body mass (kg) is measured by using a bioelectrical impedance analysis
Change in fat body mass
Fat body mass (kg) is measured by using a bioelectrical impedance analysis
Energy expenditure
Sensewear Armband
Change in Fasting glucose
Fasting glucose is measured by a blood test
Change in Fasting insulin
Fasting insulin is measured by a blood test
Change in cholesterol
Cholesterol is measured by a blood test
Change in neutrophil/lymphocyte
Neutrophil/lymphocyte is measured by a blood test
Change in C-reactive protein
C-reactive protein is measured by a blood test
Adherence
Percentage of sessions completed

Full Information

First Posted
March 17, 2017
Last Updated
January 20, 2021
Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
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1. Study Identification

Unique Protocol Identification Number
NCT03096951
Brief Title
Prehabilitation in Colorectal Cancer
Official Title
Prehabilitation Before Surgery in Colorectal Cancer With Improved Fast Track Rehabilitation : Part 1
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
April 4, 2017 (Actual)
Primary Completion Date
October 1, 2019 (Actual)
Study Completion Date
October 1, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Objectives To investigate the impact of tele-supervised prehabilitation on functional capacity in colon cancer patients undergoing colorectal resection for cancer and to evaluate the effects of prehabilitation on muscle strength and endurance, quality of life (QoL), executive functions, fatigue and inflammatory and metabolic parameters. Methods A randomized controlled trial will be conducted. Patients will be randomised into either a prehabilitation group or a control group. The prehabilitation group will receive tele-supervised prehabilitation for 4weeks and telerehabilitation for 8weeks post-surgery while control group will begin telerehabilitation only after surgery for 8weeks. Patients will care with an enhanced recovery pathway. Telerehabilitation pre and post-surgery will consist of three moderate-intensity aerobic and resistance sessions per week. Subjects will be assessed at baseline, pre-intervention, post-intervention and post-rehabilitation. The primary outcome will be functional capacity measured using the 6-min walk test. The secondary outcomes will be: physical measurement, quality of life, level of physical activity, executive functions, fatigue, body composition, blood test, energy expenditure.
Detailed Description
Study objectives Primary objective: The investigators want to assess if a tele-supervised prehabilitation improves preoperative cardio-respiratory fitness in colon cancer patients in the setting of an enhanced recovery pathway. Secondary objectives The investigators want to examine if this tele-supervised prehabilitation has beneficial effects on muscle strength and endurance, on quality of life, on executive functions, on fatigue, on inflammatory parameters and on metabolic disruption pre-surgery. The investigators want to determine whether changes in the preoperative period remain in the postoperative period after 8 weeks of telerehabilitation. Rationale and scientific background: In Belgium, colon cancer is the third most common cancer in men and the second most common in women and is the second cause of cancer death. Surgery is currently the primary treatment for stage I to III. This surgery benefits from several years of multimodal program, commonly called "Fast Track" program or enhanced recovery. Nowadays, the lack of preoperative fitness is not specifically taken into account in the Fast Track program. Nevertheless, studies have shown that patients with poor preoperative physical fitness are less able to cope with the adverse effects of surgery and hospitalization resulting in increased risk of mortality, postoperative complications and functional recovery time. It seems relevant to intervene during the preoperative period to improve the patient's functional capacity before the surgery, via physical training to overcome the stress of the surgery and to improve postoperative recovery. This process is called "prehabilitation" Structured and supervised programs have shown to be effective and feasible. However, time, resources, expensive care are often a barrier for the patient. Thereby, a home-based tele-supervising rehabilitation would be an attractive therapeutic option to offer a distinct advantage in this regard. More specifically, "telerehabilitation can be defined as the application of telecommunication, remote sensing and operation technologies, and computing technologies to assist with the provision of medical rehabilitation services at a distance". Study design A single-blind, randomized, controlled trial will be conducted. Participants will be randomized into either a prehabilitation group or a rehabilitation group. Participants in both groups will care in an Fast Track Program. An assessor who will be blinded to group allocation will collect outcomes measures for each participant. To be eligible for this study participants will need to meet the following criteria: Diagnosis of colon cancer requiring surgery; more than 50 years of age; autonomous and voluntary person; able to read, write and understand French; Participants will be excluded if the participants have a physical impairment that would seriously impair physical mobility; have an unfavorable familial context; have a stoma; have an American Society of Anesthesiologists score IV-V; the surgery is an emergency; have neuropsychiatric disease. Participants allocated to the prehabilitation group will undertake a telerehabilitation program that will start 4 weeks before the surgery and will continue during 8 weeks after the surgery. Participants in the control group will receive World Health Organization recommendations on physical activity for health before surgery. After the surgery, The control group will undertake a telerehabilitation program over an 8-week period. The telerehabilitation program will combine aerobic and resistance training three sessions per week. Each 60-min session will begin and end with a five-minute warm-up/cool. The warm-up will be followed by 25 minutes of aerobic training. Aerobic exercise can include brisk walking, jogging, cycling, or swimming according to patient's preference. The intensity of the exercise was set between 60 à 75% of maximum heart rate (maximal heart rate=220 - age). And between 12 and 16 on Borg's Rating of Perceived Exertion Scale. Each participant will wear a heart monitor. The aerobic training will be followed by resistance exercise performed on eight exercises targeting major muscle groups (abdominal, hamstring, quadriceps, triceps, gluteus maximus, paraspinal muscles and shoulder muscles). Intensity must be between 12 and 16 on the Borg's Rating of Perceived Exertion Scale. A physiotherapist will provide detailed information about the program. The patient will receive a brochure in which there will be descriptions and pictures of exercises and a video including the resistance program was recorded on a website. The researcher will conduct weekly telephone calls with the participants. The aim of these calls will be to solve any problems of carrying out the training sessions and to discuss about possible adverse events. Moreover, the researcher will give messages of support and encouragement to improve adherence to the program. Outcome measures will be assessed at four time points: at baseline (T0), one day before the scheduled date of surgery (T1), one week after the intervention (T2) and at the end of the postoperative rehabilitation (T3). Primary outcome will be cardiorespiratory fitness 6min walk test). Secondary outcomes will be muscle strength and endurance (isokinetic dynamometer and 1min sit-to-stand-test), quality of life ("Euroquol-5D-3L" questionnaire); level of physical activity (International Physical Activity Questionnaire Short Form); fatigue (Functional Assessment of Cancer Therapy: Fatigue); executive functions (Trail Making test, Stroop test and fluency) ; blood test (neutrophil lymphocyte ratio, C reactive protein, fasting glucose, fasting insulin and cholesterol will be measured by bioelectrical impedance analysis); energy expenditure ("Sensewear®" armband).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colon Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Prehabilitation group
Arm Type
Experimental
Arm Description
Preoperative and postoperative telerehabilitation
Arm Title
Rehabilitation group
Arm Type
Active Comparator
Arm Description
Postoperative telerehabilitation
Intervention Type
Behavioral
Intervention Name(s)
Prehabilitation
Intervention Description
Prehabilitation group will receive a 4-week tele-supervised prehabilitation and a 8-week tele-supervised postoperative rehabilitation.
Intervention Type
Other
Intervention Name(s)
Rehabilitation
Intervention Description
Rehabilitation group will receive World Health Organization recommendations on physical activity for health before surgery and a 8-week tele-supervised postoperative rehabilitation.
Primary Outcome Measure Information:
Title
Change in cardiorespiratory fitness
Description
Cardiorespiratory is measured by a 6-minute walk test
Time Frame
Assessments at baseline, one day before the surgery, 1 week after the surgery and immediately after the rehabilitation
Secondary Outcome Measure Information:
Title
Change in muscle strength
Description
Muscle strength is measured by using an isokinetic dynamometer
Time Frame
Assessments at baseline, one day before the surgery, immediately after the rehabilitation
Title
Change in muscle endurance
Description
Muscle endurance is measured by using the "1-minute sit-to-stand-test" (number of sit-to-stand cycles during 1 minute)
Time Frame
Assessments at baseline, one day before the surgery, 1week after the surgery and immediately after the rehabilitation
Title
Change in quality of life
Description
Quality of life is measured by using the Euroquol-5D-3L questionnaire
Time Frame
Assessments at baseline, one day before the surgery, 1week after the surgery and immediately after the rehabilitation
Title
Change in fatigue
Description
Fatigue is measured by using the Functional Assessment of Cancer Therapy: Fatigue questionnaire
Time Frame
Assessments at baseline, one day before the surgery, 1week after the surgery and immediately after the rehabilitation
Title
Change in level of physical activity
Description
Level of physical activity is measured by using the International Physical Activity Questionnaire Short Form
Time Frame
Assessments at baseline, one day before the surgery, 1week after the surgery and immediately after the rehabilitation
Title
Change in executive functions
Description
Executive functions is measured by using the Trail Making test
Time Frame
Assessments at baseline, one day before the surgery, 1 week after the surgery and immediately after the rehabilitation
Title
Change in executive functions
Description
Executive functions is measured by using the Fluency test
Time Frame
Assessments at baseline, one day before the surgery, 1 week after the surgery and immediately after the rehabilitation
Title
Change in weight
Description
Weight (kg) is measured by using a bioelectrical impedance analysis
Time Frame
Assessments at baseline, one day before the surgery, 1 week after the surgery and immediately after the rehabilitation
Title
Change in lean body mass
Description
Lean body mass (kg) is measured by using a bioelectrical impedance analysis
Time Frame
Assessments at baseline, one day before the surgery, 1 week after the surgery and immediately after the rehabilitation
Title
Change in fat body mass
Description
Fat body mass (kg) is measured by using a bioelectrical impedance analysis
Time Frame
Assessments at baseline, one day before the surgery, 1 week after the surgery and immediately after the rehabilitation
Title
Energy expenditure
Description
Sensewear Armband
Time Frame
During 7 days before the surgery and during 7 days after the surgery
Title
Change in Fasting glucose
Description
Fasting glucose is measured by a blood test
Time Frame
Assessments at baseline, one day before the surgery, 1 week after the surgery and immediately after the rehabilitation
Title
Change in Fasting insulin
Description
Fasting insulin is measured by a blood test
Time Frame
Assessments at baseline, one day before the surgery, 1 week after the surgery and immediately after the rehabilitation
Title
Change in cholesterol
Description
Cholesterol is measured by a blood test
Time Frame
Assessments at baseline, one day before the surgery, 1 week after the surgery and immediately after the rehabilitation
Title
Change in neutrophil/lymphocyte
Description
Neutrophil/lymphocyte is measured by a blood test
Time Frame
Assessments at baseline, one day before the surgery, 1 week after the surgery and immediately after the rehabilitation
Title
Change in C-reactive protein
Description
C-reactive protein is measured by a blood test
Time Frame
Assessments at baseline, one day before the surgery, 1 week after the surgery and immediately after the rehabilitation
Title
Adherence
Description
Percentage of sessions completed
Time Frame
Assessments at baseline, one day before the surgery, 1 week after the surgery and immediately after the rehabilitation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of colon cancer requiring surgery; more than 40 years of age; autonomous and voluntary person; able to read, write and understand French; Frailty phenotype criteria < 3 Exclusion Criteria: a physical impairment that would seriously impair physical mobility; an unfavorable familial context; a stoma; American Society of Anesthesiologists score IV-V; emergency; neuropsychiatric disease.
Facility Information:
Facility Name
Cliniques universitaires Saint-Luc
City
Brussels
State/Province
Woluwé-Saint-Lambert
ZIP/Postal Code
1200
Country
Belgium

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
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23485231
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Prehabilitation in Colorectal Cancer

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