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Exercise Prehabilitation in High Risk Cancer Surgery: A Feasibility Study

Exercise Prehabilitation and Pulmonary Bundle in High Risk Cancer Surgery (ExPREHAB Plus): A Feasibility Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12620000073909
Acronym
ExPREHAB Plus
Enrollment
50
Registered
2020-01-30
Start date
2018-04-17
Completion date
2019-12-19
Last updated
2021-07-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This study aims to evaluate the feasibility of delivering an individualised exercise prehabilitation program amongst high risk surgical patients presenting for major cancer surgery. Who is it for? You may be eligible to join this study if you are aged 18 years or above and are scheduled to undergo major abdominal cancer surgery. Study details Participants in this study will receive an indivdiualised exercise prehabilitation program for a period of six weeks. Potential participants are recruited through our cardiopulmonary exercise testing clinic at the Peter MacCallum Cancer Centre. Participants are then followed for a period of six weeks preoperatively and thirty days post-operatively in order to review any surgical complications, length of stay in hospital and other clinical outcomes. If preoperative exercise is feasible within this population, we may be able to implement a program for patients of high risk to lessen surgical risk post-operatively.

Interventions

Eligible participants will be prescribed an exercise program for a period of six weeks or up until surgery (whichever is earlier). Exercise prescriptions will be individualized to a participant’s prior aerobic fitness, medical comorbidities, response to any prior treatment and any immediate negative treatment effects of prior treatment (such as ongoing neuropathy and/or cancer cachexia) as per the ACSM Guidelines for exercise prescription. Exercise programs will be conducted one-on-one either

Eligible participants will be prescribed an exercise program for a period of six weeks or up until surgery (whichever is earlier). Exercise prescriptions will be individualized to a participant’s prior aerobic fitness, medical comorbidities, response to any prior treatment and any immediate negative treatment effects of prior treatment (such as ongoing neuropathy and/or cancer cachexia) as per the ACSM Guidelines for exercise prescription. Exercise programs will be conducted one-on-one either in person in a hospital-based gym or unsupervised within the home environment based on the patient's preference and ability to travel to the hospital. Exercise programs will be moderate to vigorous intensity as rated by the Borg RPE rating scale and prescribed in conjunction with cardiopulmonary exercise testing results. Exercise programs will include at least 3x30min aerobic exercise (walking/cycling/swimming) and 2x30min resistance sessions (upper and lower body strengthening exercises e.g. sit to stand, step ups, shoulder press) per week based on whether participants are meeting the ACSM exercise prescription guidelines at baseline. Participants will also be provided with a respiratory education session including information regarding breathing exercises to complete in the lead up to surgery. Given the complexity of this patient sample exercise prescription will also be adapted upon previous musculoskeletal injuries/issues (e.g. previous total joint replacements) and patients exercise preferences, to increase adherence with six-week program. Exercise programs will be progressed by a qualified physiotherapist and/or exercise physiologist based on participant’s response to exercise and compliance with the exercise program. The 30 min respiratory education session, delivered by a Physiotherapist, will include education, instruction and practice of Active Cycle of Breathing Exercises as well as education on preventing post-operative pulmonary complications by utilising breathing exercises as well as early mobilisation. Participants are encouraged to practice their breathing exercises 2x per day for 10 min. Education will delivered at any point during the six week intervention. No specific strategies will be used to monitor adherence to the breathing exercises.

Sponsors

Peter MacCallum Cancer Centre
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Eligibility criteria: • Planned to have major abdominal cancer surgery* • Adults greater than or equal to 18 years of age • English speaking • >2 weeks prior to surgery • Outpatients or in-patients with planned discharge from hospital in less than 1 week • Poor cardiorespiratory fitness determined by any one of the following: AT less than or equal to 11ml/kg/min, VO2 Peak less than or equal to 15ml/kg/min or VO2 Peak less than or equal to 710ml/min/m2 • For those unable to complete CPET: less than or equal to 70% predicted distance on the 6MWT *major cancer surgery in this study is defined as abdominal cancer surgeries with an anticipated duration of >2 hours and anticipated length of hospital stay of >1 night.

Exclusion criteria

Exclusion criteria: • Myocardial infarction in the last 3 months or unstable angina • Cerebrovascular event or transient ischemic attack in the last 3 months • Pulmonary embolic event within 3 months, existing acute or chronic deep vein thrombosis • Pregnancy • Presentation with active sepsis • Planned for surgery in <2weeks • Hospital inpatient, with anticipated admission >1 week • Unable or contra-indication to exercise • Unable to exercise unsupervised and the absence of appropriate supervision

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 11, 2026