Prehabilitation for Colorectal Cancer Patients With Low Functional Capacity and Malnutrition

Sponsor
McGill University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05999370
Collaborator
McGill University Health Centre/Research Institute of the McGill University Health Centre (Other)
60
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46
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Study Details

Study Description

Brief Summary

Despite multi-modal prehabilitation (nutrition, exercise, and psychosocial interventions), 60% of older elective colorectal cancer surgery patients with poor physical function were unable to reach a minimum preoperative 400m six-minute walking distance (6MWD), a prognostic cut-point. Compared to the patients that attained >400m 6MWD preoperatively, twice as many of <400m patients were malnourished. Malnutrition has long been associated with worse functioning (e.g., physical, immune). The investigators hypothesize that for nutritionally deficient patients, the etiology for their poor physical function is malnutrition. Correction of malnutrition alone might thus be sufficient to achieve a 400m 6MWD before surgery and improve patient outcomes.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Nutrition
  • Behavioral: Exercise
N/A

Detailed Description

The investigators propose a randomized controlled trial of nutrition prehabilitation alone vs nutrition prehabilitation with supportive exercise in patients with malnutrition and 6MWD <400m before elective colorectal surgery. The primary objective, and therapeutic target, will be achievement of minimal clinical important difference for the 6MWD (14m for within group comparisons and 19m between groups). Ability to adhere to the interventions will be monitored. The findings of this study will guide optimal treatment for this vulnerable population by exploring the role of nutrition alone vs. nutrition with exercise to optimize surgical outcomes.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Is Correction of Malnutrition Sufficient to Improve Low Physical Function Before Elective Colorectal Cancer Surgery? A Randomized Controlled Trial of Nutrition vs Nutrition and Exercise Prehabilitation
Actual Study Start Date :
Jan 31, 2022
Anticipated Primary Completion Date :
Dec 1, 2025
Anticipated Study Completion Date :
Dec 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Other: Nutrition and exercise

The nutrition intervention will be based on a comprehensive nutrition assessment by a dietitian at baseline, enabling individualized caloric and protein targets. The exercise intervention will be personalized based on a comprehensive assessment to include both a resistance and an aerobic component in the form of a "snack".

Behavioral: Nutrition
The nutrition intervention will be based on needs assessed by indirect calorimetry, patient-generated subjective global assessment, and 24hr recall conducted at baseline, enabling individualized caloric and protein targets. Deficits in nutrient intake will be addressed with one-on-one dietary counselling and supplementation at baseline in a quantity that matches the estimated deficit in intake. Adherence will be monitored using 24-hr recalls and weight status by the dietitian weekly.

Behavioral: Exercise
The exercise intervention will include both a resistance and an aerobic component to be performed a total of 5 times a day, 5 times per week, 5 minutes each session, totaling 125 minutes per week. The ability to perform exercises as prescribed will be monitored with a weekly in-person or virtual supervised session.

Other: Nutrition only

The nutrition intervention will be based on a comprehensive nutrition assessment by a dietitian at baseline, enabling individualized caloric and protein targets.

Behavioral: Nutrition
The nutrition intervention will be based on needs assessed by indirect calorimetry, patient-generated subjective global assessment, and 24hr recall conducted at baseline, enabling individualized caloric and protein targets. Deficits in nutrient intake will be addressed with one-on-one dietary counselling and supplementation at baseline in a quantity that matches the estimated deficit in intake. Adherence will be monitored using 24-hr recalls and weight status by the dietitian weekly.

Outcome Measures

Primary Outcome Measures

  1. Preoperative six-minute walking distance [from date of baseline assessment until date of surgery, an average of 4 weeks, recorded in meters]

    Physical function will be measured with the six-minute walking test (6MWT). Patients will be instructed to walk back and forth along a 20m hallway, and the distance covered in 6 minutes (6MWD) will be recorded (meters).

Secondary Outcome Measures

  1. Adherence to the exercise intervention [from date of baseline assessment until date of surgery,an average of 4 weeks, recorded in steps]

    Adherence will be monitored by use of logbooks and a smart watch (FitBit), which records daily steps.

  2. Adherence to the nutrition intervention [from date of baseline assessment until date of surgery, an average of 4 weeks, recorded in % of prescription adherence]

    Adherence to dietary targets (energy intake) will be carefully monitored by weekly in-person or virtual visit using 24hr recalls and supplement counts (energy consumption as compared to prescribed energy targets)

  3. Adherence to the nutrition intervention [from date of baseline assessment until date of surgery, an average of 4 weeks, recorded in % of prescription adherence]

    Adherence to dietary targets (protein intake) will be carefully monitored by weekly in-person or virtual visit using 24hr recalls and supplement counts (protein consumption as compared to prescribed protein targets)

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients aged 65 years and older;

  • Patients with cancer scheduled for primary colorectal resection;

  • Patients with 6MWD at baseline less than 400 m;

  • Patients with Patient-Generated Subjective-Global Assessment (malnutrition assessment) score equal or greater than 9.

Exclusion Criteria:
  • Patients with history of premorbid conditions that contraindicate exercise including dementia, -Parkinson's disease or previous stroke with paresis;

  • Metastatic cancer;

  • Patients who do not speak English or French and cannot be accompanied by someone who speaks English or French;

Contacts and Locations

Locations

Site City State Country Postal Code
1 MUHC Research Ethics Board Montréal Quebec Canada H4A 3T2

Sponsors and Collaborators

  • McGill University
  • McGill University Health Centre/Research Institute of the McGill University Health Centre

Investigators

  • Principal Investigator: Chelsia Gillis, RD PhD, McGill University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Chelsia Ann Gillis, Assistant Professor, McGill University
ClinicalTrials.gov Identifier:
NCT05999370
Other Study ID Numbers:
  • 37-2021-6990
First Posted:
Aug 21, 2023
Last Update Posted:
Aug 21, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 21, 2023