- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05579340
Postoperative Exercise Training and Colorectal Cancer Liver Metastasis (POET-mCRC)
Post-Operative Exercise Training in Patients With Metastatic Colorectal Cancer
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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Copenhagen, Denmark, 2100
- Rigshospitalet (CFAS)
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Usual care
|
|
|
Experimental: Ex1
Low exercise volume (150 min/week)
|
6 months of combined aerobic and resistance exercise
|
|
Experimental: Ex2
High exercise volume (300 min/week)
|
6 months of combined aerobic and resistance exercise
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in peak oxygen consumption (VO2peak)
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in VO2peak assessed during an incremental exercise test to volitional exhaustion on a bicycle ergometer
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
3-years overall survival
Time Frame: Randomization to 3 years after randomization
|
Proportion of patients who are alive 3 years after randomization
|
Randomization to 3 years after randomization
|
|
3-years recurrence-free survival
Time Frame: Randomization to 3 years after randomization
|
Proportion of patients who survive without relapse (formation of new tumors) for the 3-year period
|
Randomization to 3 years after randomization
|
|
Changes in Aerobic Capacity: Ventilatory threshold
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in ventilatory threshold assessed during an incremental exercise test to volitional exhaustion on a bicycle ergometer
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Aerobic Capacity: Peak power output
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in peak power output assessed during an incremental exercise test to volitional exhaustion on a bicycle ergometer
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Muscle strength: Hand grip strength
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in hand grip strength, assessed using a dynamometer
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Muscle strength: Leg press maximal muscle strength
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in leg press one repetition maximum (1RM)
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Functional performance: Habitual gait speed
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in habitual gait speed
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Functional performance: Maximal gait speed
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in maximal gait speed
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Functional performance: Stair climbing performance
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in time required to climb a specific staircase
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Functional performance: 30 seconds Sit-to-stand
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in the number of stands from sitting position that can be performed during 30 seconds
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Body composition and anthropometrics: Body mass
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in body mass
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Body composition and anthropometrics: Total lean mass
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in total lean mass assessed by dual energy x-ray absorptiometry (DXA)
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Body composition and anthropometrics: Total fat mass
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in total fat mass assessed by DXA
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Body composition and anthropometrics: Bone mineral density
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in bone mineral density assessed by DXA
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Body composition and anthropometrics: Waist circumference
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in waist circumference
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Body composition and anthropometrics: Hip circumference
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in Hip circumference
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Systolic Blood pressure
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting systolic blood pressure
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Diastolic Blood pressure
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting diastolic blood pressure
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Heart rate
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting heart rate
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Blood biochemistry: leukocyte differential counts
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting leukocyte differential counts (total and per type [eosinophils, basophils, lymphocytes, monocytes, neutrophils])
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Blood biochemistry: C-reactive protein
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting C-reactive protein levels in blood
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Blood biochemistry: Insulin
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting insulin blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Blood biochemistry: Glucose
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting glucose blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Blood biochemistry: Triglycerides
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting triglycerides blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Blood biochemistry: LDL-Cholesterol
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting LDL-cholesterol blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Blood biochemistry: HDL-Cholesterol
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting HDL-cholesterol blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Cytokine levels in blood: Interleukin-6
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting Interleukin-6 blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Cytokine levels in blood: Interleukin-1
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting Interleukin-1 blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Cytokine levels in blood: Interleukin-7
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting Interleukin-7 blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Cytokine levels in blood: Interleukin-8
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting Interleukin-8 blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Cytokine levels in blood: Interleukin-15
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting Interleukin-15 blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Cytokine levels in blood: Interleukin-1β
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting Interleukin-1β blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Cytokine levels in blood: Interleukin-10
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting Interleukin-10 blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Cytokine levels in blood: Tumor-necrosis-factor alpha (TNFalpha)
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting TNFalpha blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Cytokine levels in blood: Interferon gamma (IFN-gamma)
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting IFN-gamma blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Immune cells in blood: Natural killer (NK) cells
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting NK cells
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Immune cells in blood: CD4 T cells
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting CD4 T cells
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Immune cells in blood: CD8 T cells
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting CD8 T cells
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Immune cells in blood: B cells
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting B cells
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Osteonectin
Time Frame: Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
Changes in resting osteonectin blood levels
|
Baseline, 3-, 6-, 9- and 12 months after exercise training initiation
|
|
Changes in Patient-reported symptomatic adverse events
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
Patient-reported symptomatic adverse events, assessed using the using the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Health-related quality of life: Physical well-being
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
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)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Health-related quality of life: Social well-being
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
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)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Health-related quality of life: Emotional well-being
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
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)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Health-related quality of life: Functional well-being
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
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)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Health-related quality of life: General
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
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)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Health-related quality of life: Colorectal cancer specific
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
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)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Health-related quality of life: total score
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
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)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Health-related quality of life: Trial outcome index
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
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)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Health-related quality of life: Fatigue
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
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)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Depression
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
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)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Anxiety
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
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)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Physical activity: Walking
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
Changes in patient-reported weekly duration of walking, assessed using the International Physical Activity Questionnaire (IPAQ)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Physical activity: Moderate intensity physical activity
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
Changes in patient-reported weekly duration of moderate intensity physical activity, assessed using the International Physical Activity Questionnaire (IPAQ)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Physical activity: Vigorous intensity physical activity
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
Changes in patient-reported weekly duration of vigorous intensity physical activity, assessed using the International Physical Activity Questionnaire (IPAQ)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Physical activity: Total intensity physical activity
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
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)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Physical activity: sitting time
Time Frame: Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
Changes in patient-reported weekly sitting time, assessed using the International Physical Activity Questionnaire (IPAQ)
|
Baseline, 3-, 6-, 9-, 12-, 24- and 36 months after exercise training initiation
|
|
Changes in Circulating tumor DNA (ctDNA)
Time Frame: Baseline, 6-, and 12 months after exercise training initiation
|
Changes in ctDNA in blood
|
Baseline, 6-, and 12 months after exercise training initiation
|
|
Changes in DNA methylation
Time Frame: Baseline, 6-, and 12 months after exercise training initiation
|
Changes in DNA methylation derived from blood
|
Baseline, 6-, and 12 months after exercise training initiation
|
|
Changes in treatment tolerance: Relative dose intensity (RDI) of adjuvant chemotherapy
Time Frame: From date of planned initiation to end of adjuvant chemotherapy
|
RDI (%) of adjuvant chemotherapy, calculated as the actual dose intensity / standard dose intensity x 100%
|
From date of planned initiation to end of adjuvant chemotherapy
|
|
Postoperative hospital admissions
Time Frame: From discharge to 12 months after exercise training initiation
|
Incidence of postoperative hospital re-admissions, defined as any non-scheduled ≥ 24 h hospitalization
|
From discharge to 12 months after exercise training initiation
|
|
Postoperative complications
Time Frame: From discharge to 30 days after discharge
|
Incidence of postoperative complications up to 30 days after surgery (total and by grade and type), assessed using the Clavien-Dindo classification
|
From discharge to 30 days after discharge
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Casper Simonsen, PhD, Group Leader
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Neoplasms by Site
- Neoplasms
- Intestinal Diseases
- Gastrointestinal Neoplasms
- Digestive System Neoplasms
- Digestive System Diseases
- Gastrointestinal Diseases
- Colorectal Neoplasms
- Intestinal Neoplasms
- Colonic Diseases
- Colonic Neoplasms
- Motor Activity
- Movement
- Musculoskeletal Physiological Phenomena
- Musculoskeletal and Neural Physiological Phenomena
- Exercise
Other Study ID Numbers
- POET-mCRC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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