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Pilot Prehabilitation Intervention in Lung Cancer

Primary Purpose

Lung Cancer, Surgery

Status
Terminated
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Multimodal intervention (MM)
Sponsored by
McGill University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Lung Cancer focused on measuring Prehabilitation, Nutritional supplement

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • adult men and women with NSCLC stages I, II or IIIa, planned for video-assisted thoracic surgery (VATS) or open thoracotomy surgery for cancer resection or exploration.

Exclusion Criteria:

  • prior recent (<3 mo) chemotherapy, comorbidities contraindicating exercise (defined as CPET <10 mL O2/kg/min), walking aids other than a cane, glomerular filtration rate <30 mL/min/m2, allergy to milk or seafoods, chronic use of anti-coagulants, hypercalcemia, hypervitaminosis D, insufficient understanding of English or French language to provide informed consent. All medications and co-morbidities will be recorded. Patients taking vitamin D will continue their supplements; risk of potential overdosing will be monitored by serum 25(OH)D levels >80 nmol/L. Those taking n-3 FA supplements will be asked to withhold during the study.

Sites / Locations

  • Research Institute of the McGill University Health Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Multimodal intervention (MM)

Standard of care (SOC)

Arm Description

Multimodal prehabilitation including structured exercise (1 supervised exercise session per week + home-based exercise program), nutritional optimization (diet + mixed nutrient supplement containing whey protein, leucine, vitamin D and omega 3 fatty acids) and relaxation strategies.

Education on benefits of physical activity and healthy diet, with no specific information.

Outcomes

Primary Outcome Measures

Feasibility: Recruitment rate
Recruitment rate (measured in percent, compared to expected rates)
Feasibility: Adherence to intervention
Adherence to exercise and nutritional interventions (measured in percent, compared to expected rates)
Feasibility: completion of study outcome assessment
Completion of study outcome assessments (measured in percent, compared to expected rates)

Secondary Outcome Measures

Functional walking capacity
Six-minute walking test: measured as the distance walked during 6 minutes, along a 20-m corridor, expressed in m)
Length of hospital stay
Recorded from medical charts
Post-operative complications
Recorded from medical charts and will be graded by severity following the Clavien-Dindo classification.
Health related quality of life
Measured by the cumulative score of the 36-item Short Form Health Survey, score 0-100, higher score means better quality of life.
Quality of Life
Measured by cumulative score of the Functional Assessment of Cancer Therapy - Lung questionnaires, score 0-136, higher means better quality of life.
Muscle strength - handgrip
Handgrip strength using hand-held Jamar dynamometer, measured in kg.
Muscle strength - leg
Isokinetic leg strength (knee extension peak torque) using Biodex, measured in N, on the dominant side.
Muscle volume
Skeletal muscle volume will be measured in the dominant foreleg, using peripheral quantitative CT (pQCT, Stratec XCT2000).
Muscle radiodensity
Skeletal muscle density will be measured in the dominant foreleg, using peripheral quantitative CT (pQCT, Stratec XCT2000).
Body composition
Lean and fat mass will be measured by bioelectrical impedance (InBody 230V)

Full Information

First Posted
September 24, 2020
Last Updated
October 29, 2020
Sponsor
McGill University
Collaborators
Peri-Operative Program Charitable Foundation, MUHC-Montreal General Hospital Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT04610606
Brief Title
Pilot Prehabilitation Intervention in Lung Cancer
Official Title
A Novel Multimodal Intervention for Surgical Prehabilitation of Patients With Lung Cancer: Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Terminated
Why Stopped
Covid-19 pandemic
Study Start Date
October 11, 2019 (Actual)
Primary Completion Date
March 12, 2020 (Actual)
Study Completion Date
March 12, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
McGill University
Collaborators
Peri-Operative Program Charitable Foundation, MUHC-Montreal General Hospital Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Lung cancer is the second most prevalent cancer in Canada and the leading cause of cancer-related mortality worldwide. Patients diagnosed at earlier (non-metastatic) stages are potential candidates for surgical tumor removal. However, they often present with poor nutritional status and physical function adding to the major catabolic stress imposed by surgery that negatively impacts recovery and survival after surgery. The purpose of this study is to investigate the potential benefits of a prehabilitation program that includes a combined nutritional supplement (whey protein, leucine, vitamin D and omega-3 fatty acids) with exercise and relaxation techniques for 4 weeks before surgery and continued for 8 weeks after surgery on functional pre- and postoperative outcomes, versus standard hospital care (control). Investigators will study whether the prehabilitation program improves physical performance, muscle mass and quality of life in patients undergoing lung cancer resection. The specific objective of this pilot study is to test feasibility and adherence to intervention, and generate pilot data to inform the design of a larger trial.
Detailed Description
RATIONALE: The preoperative period is an opportune time to actively engage and empower patients in improving their functional, nutritional and mental status in anticipation of the surgical stress. Considering that lung cancer patients often present with poor nutritional status and physical function prior to surgery providing a nutritional supplement to increase protein, leucine, vitamin D and omega-3 FA intake with a structured exercise program and relaxation techniques should improve muscle mass, strength and physical performance. MAIN OBJECTIVE: to test the effect of a multimodal prehabilitation intervention (MM) combining a mixed-nutrient supplement with structured exercise training against standard of care (SOC), on functional pre- and postoperative outcomes in surgical patients with lung cancer, in an open-label RCT. The present is a pilot study aiming to generate feasibility data (recruitment rate, compliance, attrition) and preliminary outcome data to support a larger trial. STUDY DESIGN: Open-label, randomized, controlled trial of two parallel arms: multimodal intervention (MM) and standard of care (SOC). After baseline assessment, patients will be randomized to either group in a 1:2 SOC:MM ratio using a computer-generated randomization scheme by block of four, with stratification by sex and functional capacity (< or > 400 m on the 6MWT). Consecutive adult patients scheduled for elective video-assisted thoracic surgery or open thoracotomy surgery of NSCLC stages I, II or IIIa, will be approached following their first appointment with their surgeon at the MUHC-Montreal General Hospital. INTERVENTION: The EXP arm will ingest a multi-nutrient supplement consisting of whey protein + leucine and fish oil + vitamin D, perform structured exercise and relaxation techniques for 4 weeks prior to surgery and 8 weeks after surgery. Control group will received standard hospital care and education on benefits of physical activity and healthy diet. Outcome assessment will be performed at baseline, preoperative, 4 and 8 weeks postoperatively. OUTCOMES: Primary: feasibility; Secondary: physical function, muscle strength, volume and density, body composition, quality of life, length of stay and post-operative complications; Other: dietary intake, physical activity, clinical markers. STATISTICAL ANALYSIS: This is a pilot study designed to generate data on feasibility and compliance to the intervention and study tests; it is not powered for identifying statistical differences in the main outcomes. The investigators will recruit 36 participants on a 1:2 ratio (12 SOC: 24 MM).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer, Surgery
Keywords
Prehabilitation, Nutritional supplement

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Open-label, randomized, controlled trial of two parallel arms: multimodal intervention (MM) and standard of care (SOC).
Masking
None (Open Label)
Allocation
Randomized
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Multimodal intervention (MM)
Arm Type
Experimental
Arm Description
Multimodal prehabilitation including structured exercise (1 supervised exercise session per week + home-based exercise program), nutritional optimization (diet + mixed nutrient supplement containing whey protein, leucine, vitamin D and omega 3 fatty acids) and relaxation strategies.
Arm Title
Standard of care (SOC)
Arm Type
No Intervention
Arm Description
Education on benefits of physical activity and healthy diet, with no specific information.
Intervention Type
Behavioral
Intervention Name(s)
Multimodal intervention (MM)
Intervention Description
Exercise: Moderate intensity resistance and aerobic exercise, including one weekly supervised session and a home-based program. Participants were asked to 1) accumulate 30 min of aerobic exercise per day of their preferred type (ex. walking) and 2) perform 30 min of resistance exercise targeting major muscle groups, every second day for 2 sets of 8-12 reps. Nutrition: Optimize diet with protein-rich foods to meet protein intake of >1.2 g/kg/d and energy of 25-30 kcal/kg/d. The supplement consists of whey protein isolate (with the goal of reaching 1.5 g/kg/d, providing 25 g/meal), 6g of leucine, fruit-flavored fish oil added with vitamin D. Relaxation strategies: private consultations with psychology-trained personnel whereby techniques aimed at reducing anxiety are practiced. Participants are also provided with a compact disc with relaxation exercises to be used at home 2-3 times per week.
Primary Outcome Measure Information:
Title
Feasibility: Recruitment rate
Description
Recruitment rate (measured in percent, compared to expected rates)
Time Frame
Over entire recruitment period (approximately 1 year)
Title
Feasibility: Adherence to intervention
Description
Adherence to exercise and nutritional interventions (measured in percent, compared to expected rates)
Time Frame
Over 12 weeks (4 weeks pre- and 8 weeks post-surgery)
Title
Feasibility: completion of study outcome assessment
Description
Completion of study outcome assessments (measured in percent, compared to expected rates)
Time Frame
Over 12 weeks (4 weeks pre- and 8 weeks post-surgery)
Secondary Outcome Measure Information:
Title
Functional walking capacity
Description
Six-minute walking test: measured as the distance walked during 6 minutes, along a 20-m corridor, expressed in m)
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Length of hospital stay
Description
Recorded from medical charts
Time Frame
8-week postoperative
Title
Post-operative complications
Description
Recorded from medical charts and will be graded by severity following the Clavien-Dindo classification.
Time Frame
8-week postoperative
Title
Health related quality of life
Description
Measured by the cumulative score of the 36-item Short Form Health Survey, score 0-100, higher score means better quality of life.
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Quality of Life
Description
Measured by cumulative score of the Functional Assessment of Cancer Therapy - Lung questionnaires, score 0-136, higher means better quality of life.
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Muscle strength - handgrip
Description
Handgrip strength using hand-held Jamar dynamometer, measured in kg.
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Muscle strength - leg
Description
Isokinetic leg strength (knee extension peak torque) using Biodex, measured in N, on the dominant side.
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Muscle volume
Description
Skeletal muscle volume will be measured in the dominant foreleg, using peripheral quantitative CT (pQCT, Stratec XCT2000).
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Muscle radiodensity
Description
Skeletal muscle density will be measured in the dominant foreleg, using peripheral quantitative CT (pQCT, Stratec XCT2000).
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Body composition
Description
Lean and fat mass will be measured by bioelectrical impedance (InBody 230V)
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Other Pre-specified Outcome Measures:
Title
Dietary assessment
Description
Collected using 2 and 3-day food diaries.
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Plasma phospholipid n-3 FA profile
Description
Plasma lipids will be extracted with organic solvents, phospholipids isolated on thin-layer chromatography, and FAs methylated for determination by gas chromatography-flame-ionization analysis. Used as an objective measure of adherence to fish oil.
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Serum 25(OH)D
Description
Concentrations will be measured by the MUHC-Central Lab. Used as an objective measure of adherence to the supplement.
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Inflammation
Description
Will be assessed with serum C-reactive protein (hs-CRP) by MUHC-Central Lab.
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Serum albumin
Description
Will be analyzed as standard procedures by the MUHC-Central Lab.
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Pre-albumin
Description
Will be analyzed as standard procedures by the MUHC-Central Lab.
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Hemoglobin
Description
Will be analyzed as standard procedures by the MUHC-Central Lab.
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Exercise tolerance - oxygen consumption
Description
Assessed using cardiopulmonary exercise testing and measuring oxygen consumption at anaerobic threshold and peak exercise
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Exercise tolerance - workload
Description
Assessed by cardiopulmonary exercise testing at anaerobic threshold and peak exercise
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Exercise tolerance - heart rate
Description
Assessed by cardiopulmonary exercise testing and measured at anaerobic threshold and peak exercise
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Pulmonary function (FEV1)
Description
Spirometry standard methods to measure FEV1.
Time Frame
Baseline and 4-week postoperative
Title
Pulmonary function (FVC)
Description
Spirometry standard methods to measure FVC.
Time Frame
Baseline and 4-week postoperative
Title
Pulmonary function (FEV1/FVC)
Description
Spirometry standard methods to measure the FEV1/FVC ratio.
Time Frame
Baseline and 4-week postoperative
Title
Pulmonary function (FEF 25-75%)
Description
Spirometry standard methods to measure FEF 25-75 percent.
Time Frame
Baseline and 4-week postoperative
Title
Physical activity
Description
Community Healthy Activities Model Program for Seniors (CHAMPS) questionnaire, score 0 - x (no maximum score), higher mean more activity
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Anxiety/depression
Description
Hospital Anxiety and Depression Scale (questionnaire). Scoring for each item ranges from zero to three. A subscale score >8 denotes anxiety or depression.
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative
Title
Nutritional status
Description
Patient-Generated Subjective Global Assessment (PG-SGA). In general, the higher total additive scores upon initial exam correlates with more severely malnourished cases (A = well nourished, B = moderately malnourished or suspected malnutrition and C = severely malnourished).
Time Frame
Baseline, preoperative, 4-week postoperative and 8-week postoperative

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: adult men and women with NSCLC stages I, II or IIIa, planned for video-assisted thoracic surgery (VATS) or open thoracotomy surgery for cancer resection or exploration. Exclusion Criteria: prior recent (<3 mo) chemotherapy, comorbidities contraindicating exercise (defined as CPET <10 mL O2/kg/min), walking aids other than a cane, glomerular filtration rate <30 mL/min/m2, allergy to milk or seafoods, chronic use of anti-coagulants, hypercalcemia, hypervitaminosis D, insufficient understanding of English or French language to provide informed consent. All medications and co-morbidities will be recorded. Patients taking vitamin D will continue their supplements; risk of potential overdosing will be monitored by serum 25(OH)D levels >80 nmol/L. Those taking n-3 FA supplements will be asked to withhold during the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stéphanie Chevalier, PhD
Organizational Affiliation
Research Institute of the McGill University Health Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Research Institute of the McGill University Health Centre
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H4A 3J1
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
IPD sharing was not planned originally and therefore consent was not obtained for it.
Citations:
PubMed Identifier
34265218
Citation
Lawson C, Ferreira V, Carli F, Chevalier S. Effects of multimodal prehabilitation on muscle size, myosteatosis, and dietary intake of surgical patients with lung cancer - a randomized feasibility study. Appl Physiol Nutr Metab. 2021 Nov;46(11):1407-1416. doi: 10.1139/apnm-2021-0249. Epub 2021 Jul 15.
Results Reference
derived

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Pilot Prehabilitation Intervention in Lung Cancer

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