Colon Cancer Clinical Trial
Official title:
Prehabilitation Before Surgery in Colorectal Cancer With Improved Fast Track Rehabilitation : Part 2
Objectives To investigate the impact of tele-supervised prehabilitation on functional
capacity in frail colon cancer patients undergoing colorectal resection 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 (PREHAB) or a control group. Prehabilitation group will
participate in a 4-week telerehabilitation before surgery while the control group will
receive usual care and World Health Organization recommendations on physical activity for
health before surgery. Program exercise will consist of three moderate-intensity aerobic and
resistance sessions per week. Subjects will have assessments at baseline, pre-intervention
and 8 weeks after surgery. The primary outcome will be functional capacity measured by using
the 6-min walk test. The secondary outcomes will be: physical measurements, QoL, level of
physical activity, executive functions, fatigue, body composition, blood test, energy
expenditure.
Objectives Primary objective: To assess if a 4-week tele-supervised prehabilitation is
effective in improving post-operative cardio-respiratory fitness in frail colon cancer
patients.
Secondary objectives : To examine if a 4-week preoperative 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.
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. 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. Moreover, approximately 60% of colon cancer patients are older than
70 years at diagnosis and more than 50% of older cancer patients have frailty or pre-frailty.
Frailty is a state of vulnerability decreased functional reserve, impairment or dysregulation
in several physiological systems, and reduced capacity to recover physiological homeostasis
after a stress. Nowadays, no frail definition is clearly defined. One widely accepted
definition uses the Fried criteria including the assessment of weight loss, physical
exhaustion, physical activity level, grip strength and walking speed. Preoperative frail
colon cancer patients have a significantly higher risk of adverse postoperative outcomes
including institutionalization, length of stay, morbidity and mortality. 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 and 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. To
date, no study has studied the effects of tele-supervised prehabilitation in these "frail"
patients.
Study design A single-blind, randomized, controlled trial will be conducted. Participants
will be randomized into either a prehabilitation group or a control group. An assessor who
will be blinded to group allocation will collect outcomes measures for each participant.
Study sample To be eligible for this study participants will need to meet the following
criteria: diagnosis of colon cancer requiring surgery; more than 65 years of age; able to
read, write and understand French; Frailty phenotype criteria ≥ 3. Frailty was assessed using
the components of the Frailty Phenotype, which was first developed by Fried et al., which
consists of five criteria: weight loss, exhaustion, low physical activity, slowness, and
weakness.
Participants will be excluded if they have a physical impairment that would seriously impair
physical mobility; the surgery is an emergency; have a neuropsychiatric disease.
Intervention Participants allocated to the prehabilitation group will undertake a
telerehabilitation program that will start 4 weeks before the surgery while participants in
the control group will receive usual care and World Health Organization recommendations on
physical activity for health before surgery.
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 Outcome measures will be assessed at three time points: at baseline (T0),
one day before the scheduled date of surgery (T1) and 8 weeks after the surgery (T2).
Primary outcome will be cardiorespiratory fitness 6min walk test). Secondary outcomes will be
muscle strength and endurance (isokinetic dynamometer and 1-min sit-to-stand-test), quality
of life (EQ-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 and fluency verbal test) ; 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).
;
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