Clinical

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Prehabilitation for Gastrointestinal Cancer Surgery


ABSTRACT: Interventions: The intervention will commence from time of preadmission clinic assessment or direct screening from the surgeon’s rooms, allowing for a duration of 2-4 weeks. The prehabilitation intervention will consist of 1.Exercise: Consisting of one-two supervised, tailored 60-minute group-based exercise sessions per week delivered by an accredited exercise physiologist at the Survivorship Gym, Concord Hospital. Exercise sessions will be a combination of aerobic (AET) and resistance (RET) exercise training ranging from low, moderate to vigorous intensity. AET may include the use of a cycle ergometer, treadmill, elliptical and/or rowing machine. Target intensity of AET is 60-75% of heart rate reserve. Selection of apparatus will be dependent on participant preference and capability. RET will be of large muscle groups and use body weight, hand weights and/or cable machine exercises, e.g. bicep curls, shoulder press, bench press, push ups and sit-ups. Heart rate and Rating of Perceived Exertion (RPE) will be recorded throughout each session along with the intensity. Attendance to the exercise sessions will be recorded. Participants will be advised to participate in a home-based AET program tailored to their baseline ability. The target is to walk, cycle, and/or swim (dependent on preference) on (at least) three other days per week and to increase each bout of exercise to build up to a total of 30 minutes of home-based aerobic exercise (walking/cycling/swimming etc) on at least three days/week prior to their surgery. Participants will be provided with an exercise diary to capture the duration, intensity and type of activity. 2.Nutrition: Nutrition assessment and dietary advice (1 x 60 minutes total) will be provided by an accredited practicing dietitian at Primary outcome(s): Adoption of the prehabilitation program. This will be measured through multiple (composite) endpoints such as referral data into the program via data linkage and logs, clinician satisfaction measured using a in-house developed evolution questionnaire to the medical team and nurses. [End of study duration, approximately 12 months. ];Reach (number, proportion, and representativeness) of individuals who are willing to participate in the prehabiliation program. This will be measured through multiple (composite) endpoints such as participation rates among eligible patients using the screening logs, and participant characteristics including demographics, tumour type, functionality (and comparison to non-participants) obtained through medical records. [End of study duration, approximately 12 months. ];Implementation of the prehabiliation program. This will be measured through multiple (composite) endpoints such as completion rates, withdrawal rates and reasons through screening logs; and adherence to exercise sessions, nurse calls and nutrition intervention through exercise and supplement diary, gym attendance, and completion of evaluations. [End of study duration, approximately 12 months. ] Study Design: Purpose: Prevention; Allocation: Non-randomised trial; Masking: Open (masking not used);Assignment: Single group;Type of endpoint: Efficacy

DISEASE(S): Gastrointestinal Cancer Surgery,Surgery-other Surgery,Cancer-bowel-anal,Cancer-bowel-small Bowel (duodenum And Ileum),Cancer-pancreatic,Cancer-stomach,Gastrointestinal Cancer,Diet And Nutrition-other Diet And Nutrition Disorders,Physical Medicine / Rehabilitation-other Physical Medicine / Rehabilitation,Cancer-bowel-back Passage (rectum) Or Large Bowel (colon),Cancer-oesophageal (gullet),Cancer-liver

PROVIDER: 2470629 | ecrin-mdr-crc |

REPOSITORIES: ECRIN MDR

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