search
Back to results

Postoperative Exercise Training and Colorectal Cancer Liver Metastasis (mCRC-POET)

Primary Purpose

Cancer Metastatic to Liver, Cancer Colorectal

Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Exercise
Sponsored by
Rigshospitalet, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cancer Metastatic to Liver

Eligibility Criteria

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

Inclusion Criteria:

  • Colorectal cancer patients diagnosed with liver metastasis and scheduled for liver metastasis surgical resection

Exclusion Criteria:

  • Age <18
  • Pregnancy
  • Physical or mental disabilities that prohibit execution of test or training procedures
  • Inability to understand the Danish language.

Sites / Locations

  • Rigshospitalet (CFAS)Recruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Experimental

Experimental

Arm Label

Usual care

Ex1

Ex2

Arm Description

Low exercise volume (150 min/week)

High exercise volume (300 min/week)

Outcomes

Primary Outcome Measures

Change in peak oxygen consumption (VO2peak)
Changes in VO2peak assessed during an incremental exercise test to volitional exhaustion on a bicycle ergometer

Secondary Outcome Measures

3-years recurrence-free survival
Proportion of patients who survive without relapse (formation of new tumors) for the 3-year period
3-years overall survival
Proportion of patients who are alive 3 years after randomization
Changes in Aerobic Capacity: Ventilatory threshold
Changes in ventilatory threshold assessed during an incremental exercise test to volitional exhaustion on a bicycle ergometer
Changes in Aerobic Capacity: Peak power output
Changes in peak power output assessed during an incremental exercise test to volitional exhaustion on a bicycle ergometer
Changes in Muscle strength: Hand grip strength
Changes in hand grip strength, assessed using a dynamometer
Changes in Muscle strength: Leg press maximal muscle strength
Changes in leg press one repetition maximum (1RM)
Changes in Functional performance: Habitual gait speed
Changes in habitual gait speed
Changes in Functional performance: Maximal gait speed
Changes in maximal gait speed
Changes in Functional performance: Stair climbing performance
Changes in time required to climb a specific staircase
Changes in Functional performance: 30 seconds Sit-to-stand
Changes in the number of stands from sitting position that can be performed during 30 seconds
Changes in Body composition and anthropometrics: Body mass
Changes in body mass
Changes in Body composition and anthropometrics: Total lean mass
Changes in total lean mass assessed by dual energy x-ray absorptiometry (DXA)
Changes in Body composition and anthropometrics: Total fat mass
Changes in total fat mass assessed by DXA
Changes in Body composition and anthropometrics: Bone mineral density
Changes in bone mineral density assessed by DXA
Changes in Body composition and anthropometrics: Waist circumference
Changes in waist circumference
Changes in Body composition and anthropometrics: Hip circumference
Changes in Hip circumference
Changes in Systolic Blood pressure
Changes in resting systolic blood pressure
Changes in Diastolic Blood pressure
Changes in resting diastolic blood pressure
Changes in Heart rate
Changes in resting heart rate
Changes in Blood biochemistry: leukocyte differential counts
Changes in resting leukocyte differential counts (total and per type [eosinophils, basophils, lymphocytes, monocytes, neutrophils])
Changes in Blood biochemistry: C-reactive protein
Changes in resting C-reactive protein levels in blood
Changes in Blood biochemistry: Insulin
Changes in resting insulin blood levels
Changes in Blood biochemistry: Glucose
Changes in resting glucose blood levels
Changes in Blood biochemistry: Triglycerides
Changes in resting triglycerides blood levels
Changes in Blood biochemistry: LDL-Cholesterol
Changes in resting LDL-cholesterol blood levels
Changes in Blood biochemistry: HDL-Cholesterol
Changes in resting HDL-cholesterol blood levels
Changes in Cytokine levels in blood: Interleukin-6
Changes in resting Interleukin-6 blood levels
Changes in Cytokine levels in blood: Interleukin-1
Changes in resting Interleukin-1 blood levels
Changes in Cytokine levels in blood: Interleukin-7
Changes in resting Interleukin-7 blood levels
Changes in Cytokine levels in blood: Interleukin-8
Changes in resting Interleukin-8 blood levels
Changes in Cytokine levels in blood: Interleukin-15
Changes in resting Interleukin-15 blood levels
Changes in Cytokine levels in blood: Interleukin-1β
Changes in resting Interleukin-1β blood levels
Changes in Cytokine levels in blood: Interleukin-10
Changes in resting Interleukin-10 blood levels
Changes in Cytokine levels in blood: Tumor-necrosis-factor alpha (TNFalpha)
Changes in resting TNFalpha blood levels
Changes in Cytokine levels in blood: Interferon gamma (IFN-gamma)
Changes in resting IFN-gamma blood levels
Changes in Immune cells in blood: Natural killer (NK) cells
Changes in resting NK cells
Changes in Immune cells in blood: CD4 T cells
Changes in resting CD4 T cells
Changes in Immune cells in blood: CD8 T cells
Changes in resting CD8 T cells
Changes in Immune cells in blood: B cells
Changes in resting B cells
Changes in Osteonectin
Changes in resting osteonectin blood levels
Changes in Patient-reported symptomatic adverse events
Patient-reported symptomatic adverse events, assessed using the using the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
Changes in Health-related quality of life: Physical well-being
Changes in patient-reported physical well-being assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-28, the higher the score the better quality of life)
Changes in Health-related quality of life: Social well-being
Changes in patient-reported social well-being assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-28, the higher the score the better quality of life)
Changes in Health-related quality of life: Emotional well-being
Changes in patient-reported emotional well-being assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-24, the higher the score the better quality of life)
Changes in Health-related quality of life: Functional well-being
Changes in patient-reported functional well-being assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-28, the higher the score the better quality of life)
Changes in Health-related quality of life: General
Changes in patient-reported general health-related qualify of life assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-108, the higher the score the better quality of life)
Changes in Health-related quality of life: Colorectal cancer specific
Changes in patient-reported colorectal-cancer specific health-related quality of life assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-28, the higher the score the better quality of life)
Changes in Health-related quality of life: total score
Changes in patient-reported in health-related quality of life (total score) assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-136, the higher the score the better quality of life)
Changes in Health-related quality of life: Trial outcome index
Changes in patient-reported trial outcome index assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-84, the higher the score the better quality of life)
Changes in Health-related quality of life: Fatigue
Changes in patient-reported fatigue assessed using the Functional Assessment of Cancer Therapy - Fatigue scale (FACIT-Fatigue) (scale score: 0-52, the higher the score the less fatigue)
Changes in Depression
Changes in patient-reported depression, assessed using the Hospital Anxiety and Depression Scale (HADS) (scale scoring: 0-21, the higher the score the worse the condition)
Changes in Anxiety
Changes in patient-reported anxiety, assessed using the Hospital Anxiety and Depression Scale (HADS) (scale scoring: 0-21, the higher the score the worse the condition)
Changes in Physical activity: Walking
Changes in patient-reported weekly duration of walking, assessed using the International Physical Activity Questionnaire (IPAQ)
Changes in Physical activity: Moderate intensity physical activity
Changes in patient-reported weekly duration of moderate intensity physical activity, assessed using the International Physical Activity Questionnaire (IPAQ)
Changes in Physical activity: Vigorous intensity physical activity
Changes in patient-reported weekly duration of vigorous intensity physical activity, assessed using the International Physical Activity Questionnaire (IPAQ)
Changes in Physical activity: Total intensity physical activity
Changes in patient-reported weekly duration of total intensity physical activity, assessed using the International Physical Activity Questionnaire (IPAQ) (Expressed as metabolic equivalent (MET)-min per week: MET level x minutes of activity x events per week)
Changes in Physical activity: sitting time
Changes in patient-reported weekly sitting time, assessed using the International Physical Activity Questionnaire (IPAQ)
Changes in Circulating tumor DNA (ctDNA)
Changes in ctDNA in blood
Changes in DNA methylation
Changes in DNA methylation derived from blood
Changes in treatment tolerance: Relative dose intensity (RDI) of adjuvant chemotherapy
RDI (%) of adjuvant chemotherapy, calculated as the actual dose intensity / standard dose intensity x 100%
Postoperative hospital admissions
Incidence of postoperative hospital re-admissions, defined as any non-scheduled ≥ 24 h hospitalization
Postoperative complications
Incidence of postoperative complications up to 30 days after surgery (total and by grade and type), assessed using the Clavien-Dindo classification

Full Information

First Posted
September 22, 2022
Last Updated
April 27, 2023
Sponsor
Rigshospitalet, Denmark
search

1. Study Identification

Unique Protocol Identification Number
NCT05579340
Brief Title
Postoperative Exercise Training and Colorectal Cancer Liver Metastasis
Acronym
mCRC-POET
Official Title
Post-Operative Exercise Training in Patients With Metastatic Colorectal Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 2023 (Anticipated)
Primary Completion Date
April 2025 (Anticipated)
Study Completion Date
April 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark

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
Up to 25% of colorectal cancer (CRC) patients are diagnosed with liver metastases, which is the most common site of metastasis, already during the primary tumor diagnosis. Another 30% of the patients will develop liver metastases at a later stage. Even though patient can be treated by surgical resection of the metastatic tumor, 50-75% of the patients experience a relapse in less than two years. Due to the high probability of relapse, mCRC patients undergo multiple rounds of surgery and adjuvant treatment (chemotherapy/radiotherapy) which results in substantial physical de-conditioning. Physical activity has been shown to increase the progression-free survival rates in mCRC patients, when applied post-diagnosis. Increased cardiorespiratory fitness (VO2peak) at the time of diagnosis among CRC individuals has been associated with lower risk of all-cause mortality. Although data on the effect of chronic exercise on VO2peak have emerged, thus far, there is no randomized clinical trial that has investigated the effects of exercise training in mCRC patients early after surgical treatment with curative intent. Therefore, this project aims to address the beneficial effect of structured exercise training primarily on VO2peak and tumor recurrence in mCRC patients immediately after surgical treatment and while they are undergoing adjuvant chemotherapy/radiotherapy. A total of 66 participants will be recruited from the Department of Surgery and Transplantation, Rigshospitalet and randomly allocated to a standard care control group (n=22), standard care plus 150 min/week exercise training (n=22) or standard care plus 300 min/week exercise training (n=22). Participants will undergo exercise training for 6 months, starting immediately after surgery, and they will be followed for additional 6 months. Tumor recurrence will be evaluated up to 3 years after training initiation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer Metastatic to Liver, Cancer Colorectal

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
66 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Usual care
Arm Type
No Intervention
Arm Title
Ex1
Arm Type
Experimental
Arm Description
Low exercise volume (150 min/week)
Arm Title
Ex2
Arm Type
Experimental
Arm Description
High exercise volume (300 min/week)
Intervention Type
Other
Intervention Name(s)
Exercise
Intervention Description
6 months of combined aerobic and resistance exercise
Primary Outcome Measure Information:
Title
Change in peak oxygen consumption (VO2peak)
Description
Changes in VO2peak assessed during an incremental exercise test to volitional exhaustion on a bicycle ergometer
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Secondary Outcome Measure Information:
Title
3-years recurrence-free survival
Description
Proportion of patients who survive without relapse (formation of new tumors) for the 3-year period
Time Frame
Randomization to 3 years after randomization
Title
3-years overall survival
Description
Proportion of patients who are alive 3 years after randomization
Time Frame
Randomization to 3 years after randomization
Title
Changes in Aerobic Capacity: Ventilatory threshold
Description
Changes in ventilatory threshold assessed during an incremental exercise test to volitional exhaustion on a bicycle ergometer
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Aerobic Capacity: Peak power output
Description
Changes in peak power output assessed during an incremental exercise test to volitional exhaustion on a bicycle ergometer
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Muscle strength: Hand grip strength
Description
Changes in hand grip strength, assessed using a dynamometer
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Muscle strength: Leg press maximal muscle strength
Description
Changes in leg press one repetition maximum (1RM)
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Functional performance: Habitual gait speed
Description
Changes in habitual gait speed
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Functional performance: Maximal gait speed
Description
Changes in maximal gait speed
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Functional performance: Stair climbing performance
Description
Changes in time required to climb a specific staircase
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Functional performance: 30 seconds Sit-to-stand
Description
Changes in the number of stands from sitting position that can be performed during 30 seconds
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Body composition and anthropometrics: Body mass
Description
Changes in body mass
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Body composition and anthropometrics: Total lean mass
Description
Changes in total lean mass assessed by dual energy x-ray absorptiometry (DXA)
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Body composition and anthropometrics: Total fat mass
Description
Changes in total fat mass assessed by DXA
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Body composition and anthropometrics: Bone mineral density
Description
Changes in bone mineral density assessed by DXA
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Body composition and anthropometrics: Waist circumference
Description
Changes in waist circumference
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Body composition and anthropometrics: Hip circumference
Description
Changes in Hip circumference
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Systolic Blood pressure
Description
Changes in resting systolic blood pressure
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Diastolic Blood pressure
Description
Changes in resting diastolic blood pressure
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Heart rate
Description
Changes in resting heart rate
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Blood biochemistry: leukocyte differential counts
Description
Changes in resting leukocyte differential counts (total and per type [eosinophils, basophils, lymphocytes, monocytes, neutrophils])
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Blood biochemistry: C-reactive protein
Description
Changes in resting C-reactive protein levels in blood
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Blood biochemistry: Insulin
Description
Changes in resting insulin blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Blood biochemistry: Glucose
Description
Changes in resting glucose blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Blood biochemistry: Triglycerides
Description
Changes in resting triglycerides blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Blood biochemistry: LDL-Cholesterol
Description
Changes in resting LDL-cholesterol blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Blood biochemistry: HDL-Cholesterol
Description
Changes in resting HDL-cholesterol blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Cytokine levels in blood: Interleukin-6
Description
Changes in resting Interleukin-6 blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Cytokine levels in blood: Interleukin-1
Description
Changes in resting Interleukin-1 blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Cytokine levels in blood: Interleukin-7
Description
Changes in resting Interleukin-7 blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Cytokine levels in blood: Interleukin-8
Description
Changes in resting Interleukin-8 blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Cytokine levels in blood: Interleukin-15
Description
Changes in resting Interleukin-15 blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Cytokine levels in blood: Interleukin-1β
Description
Changes in resting Interleukin-1β blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Cytokine levels in blood: Interleukin-10
Description
Changes in resting Interleukin-10 blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Cytokine levels in blood: Tumor-necrosis-factor alpha (TNFalpha)
Description
Changes in resting TNFalpha blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Cytokine levels in blood: Interferon gamma (IFN-gamma)
Description
Changes in resting IFN-gamma blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Immune cells in blood: Natural killer (NK) cells
Description
Changes in resting NK cells
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Immune cells in blood: CD4 T cells
Description
Changes in resting CD4 T cells
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Immune cells in blood: CD8 T cells
Description
Changes in resting CD8 T cells
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Immune cells in blood: B cells
Description
Changes in resting B cells
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Osteonectin
Description
Changes in resting osteonectin blood levels
Time Frame
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
Title
Changes in Patient-reported symptomatic adverse events
Description
Patient-reported symptomatic adverse events, assessed using the using the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Health-related quality of life: Physical well-being
Description
Changes in patient-reported physical well-being assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-28, the higher the score the better quality of life)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Health-related quality of life: Social well-being
Description
Changes in patient-reported social well-being assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-28, the higher the score the better quality of life)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Health-related quality of life: Emotional well-being
Description
Changes in patient-reported emotional well-being assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-24, the higher the score the better quality of life)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Health-related quality of life: Functional well-being
Description
Changes in patient-reported functional well-being assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-28, the higher the score the better quality of life)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Health-related quality of life: General
Description
Changes in patient-reported general health-related qualify of life assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-108, the higher the score the better quality of life)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Health-related quality of life: Colorectal cancer specific
Description
Changes in patient-reported colorectal-cancer specific health-related quality of life assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-28, the higher the score the better quality of life)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Health-related quality of life: total score
Description
Changes in patient-reported in health-related quality of life (total score) assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-136, the higher the score the better quality of life)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Health-related quality of life: Trial outcome index
Description
Changes in patient-reported trial outcome index assessed using the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) (scale scoring 0-84, the higher the score the better quality of life)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Health-related quality of life: Fatigue
Description
Changes in patient-reported fatigue assessed using the Functional Assessment of Cancer Therapy - Fatigue scale (FACIT-Fatigue) (scale score: 0-52, the higher the score the less fatigue)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Depression
Description
Changes in patient-reported depression, assessed using the Hospital Anxiety and Depression Scale (HADS) (scale scoring: 0-21, the higher the score the worse the condition)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Anxiety
Description
Changes in patient-reported anxiety, assessed using the Hospital Anxiety and Depression Scale (HADS) (scale scoring: 0-21, the higher the score the worse the condition)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Physical activity: Walking
Description
Changes in patient-reported weekly duration of walking, assessed using the International Physical Activity Questionnaire (IPAQ)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Physical activity: Moderate intensity physical activity
Description
Changes in patient-reported weekly duration of moderate intensity physical activity, assessed using the International Physical Activity Questionnaire (IPAQ)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Physical activity: Vigorous intensity physical activity
Description
Changes in patient-reported weekly duration of vigorous intensity physical activity, assessed using the International Physical Activity Questionnaire (IPAQ)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Physical activity: Total intensity physical activity
Description
Changes in patient-reported weekly duration of total intensity physical activity, assessed using the International Physical Activity Questionnaire (IPAQ) (Expressed as metabolic equivalent (MET)-min per week: MET level x minutes of activity x events per week)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Physical activity: sitting time
Description
Changes in patient-reported weekly sitting time, assessed using the International Physical Activity Questionnaire (IPAQ)
Time Frame
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
Title
Changes in Circulating tumor DNA (ctDNA)
Description
Changes in ctDNA in blood
Time Frame
Baseline, 6-, and 12 months after exercise training initiation
Title
Changes in DNA methylation
Description
Changes in DNA methylation derived from blood
Time Frame
Baseline, 6-, and 12 months after exercise training initiation
Title
Changes in treatment tolerance: Relative dose intensity (RDI) of adjuvant chemotherapy
Description
RDI (%) of adjuvant chemotherapy, calculated as the actual dose intensity / standard dose intensity x 100%
Time Frame
From date of planned initiation to end of adjuvant chemotherapy
Title
Postoperative hospital admissions
Description
Incidence of postoperative hospital re-admissions, defined as any non-scheduled ≥ 24 h hospitalization
Time Frame
From discharge to 12 months after exercise training initiation
Title
Postoperative complications
Description
Incidence of postoperative complications up to 30 days after surgery (total and by grade and type), assessed using the Clavien-Dindo classification
Time Frame
From discharge to 30 days after discharge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Colorectal cancer patients diagnosed with liver metastasis and scheduled for liver metastasis surgical resection Exclusion Criteria: Age <18 Pregnancy Physical or mental disabilities that prohibit execution of test or training procedures Inability to understand the Danish language.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christina Yfanti, PhD
Phone
+4535457641
Email
christina.yfanti@regionh.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Casper Simonsen, PhD
Phone
+4535457641
Email
casper.simonsen@regionh.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Casper Simonsen, PhD
Organizational Affiliation
Group Leader
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rigshospitalet (CFAS)
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christina Yfanti, PhD
Email
christina.yfanti@regionh.dk
First Name & Middle Initial & Last Name & Degree
Casper Simonsen, PhD
Email
casper.simonsen@regionh.dk

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Postoperative Exercise Training and Colorectal Cancer Liver Metastasis

We'll reach out to this number within 24 hrs