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Trimodal Prehabilitation in Colorectal Cancer Patients

NCT05880992 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2024-06-21

No results posted yet for this study

Summary

The goal of this clinical pilot is to determine the feasibility of implementing trimodal prehabilitation within the current perioperative infrastructure in patients having major colorectal surgery for resection of a cancer (CRC). Trimodal prehabilitation includes exercise, nutrition and mindfulness coaching and support which has been shown to improve physical status, mental preparation and to reduce loss of lean body mass in CRC patients. The primary questions this study aims to answer are: Is delivery of trimodal prehabilitation feasible within our current perioperative infrastructure and does prehabilitation impact outcomes in these patients? Researchers will compare this newly recruited prehabilitation cohort to a historical cohort of patients who did not receive prehabilitation in terms of mortality, length of stay, complications, readmissions, emergency department visits and non-home discharge.

Conditions

Interventions

BEHAVIORAL

Exercise

Aerobic and Strength exercises (equipment free, simple, modifiable)

DIETARY_SUPPLEMENT

Nutrition

Counselling on daily protein target of 1.2 g/kg as well as supplementation with protein shake (provided)

BEHAVIORAL

Mindfulness

Deep (box) breathing completing in the morning, evening and as needed.

Sponsors & Collaborators

  • Jordan Leitch

    lead OTHER

Principal Investigators

  • Jordan Leitch · Queen's University

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-07-24
Primary Completion
2024-12-31
Completion
2025-06-30

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05880992 on ClinicalTrials.gov