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EDICT - Exercise inDuced Changes In Colorectal Cancer Tissues (EDICT)

Primary Purpose

Colorectal Cancer

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Exercise programme
Muscle biopsy
Sponsored by
The Royal Bournemouth Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Colorectal Cancer focused on measuring Resectable, non-metastatic, colorectal, carcinoma, cancer, neoplasm, exercise, effects, program, pre-operative, proliferation, diagnosed, surgery, biopsy, muscle, signalling, IGF1, ki67, p53, response, training, biochemical, pathways, glucose

Eligibility Criteria

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

Inclusion Criteria:

  • Colorectal cancer confirmed by histology
  • Considered fit for surgery by surgical and anaesthetic team
  • Considered fit for physical activity programme by MDT
  • Age ≥ 18 years
  • BMI ≥ 26 kg/m2
  • Not pregnant
  • Non obstructing cancer
  • Able to provide written informed consent
  • Patients not having neoadjuvant chemotherapy

Exclusion Criteria:

  • Receiving hormone therapy
  • Patients with diabetes
  • Patients currently on either a dietary or exercise programme reflective of the World Cancer Research Fund Guidelines.
  • Cardiac or renal impairment
  • Excessive use of laxatives
  • History of eating disorders
  • Patients with inflammatory bowel disorders/coeliac
  • Strong family history/polyposis (i.e. more than one 1st degree relative <55yrs)
  • Patients with previous or concurrent malignancies

Sites / Locations

  • The Royal Bournemouth Hospital
  • Poole Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Exercise programme

Arm Description

Exercise programme Muscle biopsies

Outcomes

Primary Outcome Measures

Assess the feasibility of carrying out a two week preoperative exercise program in patients with colorectal cancer and assess the effects of preoperative exercise on the proliferation of colorectal cancer cells
To assess the feasibility of carrying out a two week preoperative exercise program in patients with colorectal cancer and to assess the effects of preoperative exercise on the proliferation of colorectal cancer cells by measuring the change in the percentage of cells staining positive for Ki67 (a measure of cell proliferation).

Secondary Outcome Measures

Changes in molecular markers for the effects of exercise and/or diet on AMPK/ mammilian target of rapamycin signalling pathway
Measuring changes in molecular markers for the effects of exercise and/or diet on AMPK/mTOR signalling pathway (phosphorylated 4EBP1 (P4EBP1), phosphorylated protein kinase B (PPKB/AKT), and phosphorylated AMPK (PAMPK).
Changes in AKT expression normal colonic tissue
Measuring changes in AKT expression normal colonic tissue - Intensity of AKT1/AKT2 staining, or AKT phosphorylation, a marker of insulin receptor signalling in cells.
Assessing Apoptosis index
Assessing Apoptosis index - Percentage of tumour cells staining positive for DNA fragmentation, a marker of cells undergoing apoptosis and therefore cell death.
Changes in molecular markers that may mediate or modify exercise/dietary effects in tumour tissues
Measuring changes in molecular markers that may mediate or modify exercise/dietary effects in tumour tissues (IR, IGF1R, p53 and its transcriptional target p21, ER, progesterone receptor, tumor necrosis factor-alpha converting enzyme and TIMP3).
Assessing gene expression profiles
Assessing gene expression profiles focusing on gene associated with insulin resistance.
Assessing the 11 gene signature
Assessing the 11 gene signature that help to predict maximal oxygen uptake gain in patients before and after exercise
Blood methylation profiles.
Blood methylation profiles.
Cortisol levels
Cortisol levels to evaluate levels of biological stress.
Postoperative complications up to 30 days postoperatively
Postoperative complications up to 30 days postoperatively
Moderator variables
Moderator variables including state of motivational readiness for exercise, weight change, depression and anxiety
Irisin levels
Irisin levels before and after exercise

Full Information

First Posted
February 5, 2014
Last Updated
March 9, 2018
Sponsor
The Royal Bournemouth Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02056691
Brief Title
EDICT - Exercise inDuced Changes In Colorectal Cancer Tissues
Acronym
EDICT
Official Title
Clinical and Biological Effects of a Preoperative Exercise Programme in Colorectal Tumour and Skeletal Muscle Tissues (Exercise inDuced Changes In Colorectal Cancer Tissues)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
October 2014 (undefined)
Primary Completion Date
September 19, 2017 (Actual)
Study Completion Date
October 30, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Royal Bournemouth Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This pilot study looks to explore the biological effects of exercise on cancer and muscle cells using a two week exercise program (HIThigh intensity training) on 20 patients with newly diagnosed and operable colorectal cancer following diagnosis and prior to surgery. Maximal oxygen uptake will also be measured. The aim of this pilot is to assess the feasibility of recruiting participants to and carrying out a two week preoperative exercise program in patients with colorectal cancer.
Detailed Description
Patients undergoing investigation for symptoms of colorectal cancer presenting to the hospital will undergo standard diagnostic procedures. Once resectable nonmetastatic cancer has been diagnosed (i.e. cancer that has not spread beyond the bowel), is amenable to surgical resection as decided by the colorectal multidisciplinary and if the patient fulfills the selection criteria, they will be asked if they wish to participate in the study. They will be given information regarding the study at the time of diagnosis. If they give their consent then a formal consenting process will take place at the next routine appointment. During this appointment the patient will have the opportunity to ask questions. A member of the study team will explain the study in detail, answer any questions potential participants (and their partners/ carers) have. The patient is free to refuse participation or withdraw from the study at any time without this affecting their care, this is explained in the information and will be discussed further at the time of informed consent. If the patient agrees to participate in the trial, following the provision of informed consent and before embarking on the exercise programme they will need to fill in two questionnaires, the International Physical Activity Questionnaire (Long) and Dietary Intervention in Primary Care Questionnaire (DINE). They will be counseled to try and maintain their normal exercise level and their calorie intake. Blood samples will also be taken, analyzed and stored for further analysis including possible genetic analysis at a later stage before starting the exercise regime. They will have a muscle biopsy under local anaesthetic taken from the thigh, again for analysis and storage. Participants will undergo an initial assessment of their baseline exercise ability and oxygen absorption using an upright exercise bike with concurrent ECG readings and breath analysis. The two week preoperative exercise regime will be planned depending on the patient's operation date. The exercise regime consists of 10 sessions of exercise against a constant load, each lasting 60s, separated by 60s of recovery eliciting 90% maximal heart rate. The 6 sessions are held over a 2 week period. Each patients exercise ability and oxygen absorption will be remeasured at the end of the 2 week period and a second sample of blood taken for comparison. During the operation a sample of adipose tissue near the tumour site will be taken separately to the main sample. A muscle biopsy from the thigh will also be taken at the same time. As a standard of clinical care all patients are reviewed in the outpatient setting 6 weeks postoperatively. When patients attend this follow up appointment a final blood test and muscle biopsy (under local anaesthetic) will be taken to assess the longer term effects of the exercise program. Patient consent will be sought for this separately although it will be discussed at the initial introduction to the study. Patients are free to withdraw from the study at any time and if there are any adverse events or concerns regarding the continuation of the study for a patient then they will be withdrawn.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
Resectable, non-metastatic, colorectal, carcinoma, cancer, neoplasm, exercise, effects, program, pre-operative, proliferation, diagnosed, surgery, biopsy, muscle, signalling, IGF1, ki67, p53, response, training, biochemical, pathways, glucose

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise programme
Arm Type
Experimental
Arm Description
Exercise programme Muscle biopsies
Intervention Type
Procedure
Intervention Name(s)
Exercise programme
Intervention Description
The exercise regime consists of 10 sessions of exercise against a constant load, each lasting 60 seconds, separated by 60 seconds of recovery eliciting 90% maximal heart rate. The 6 sessions are held over a 2 week period.
Intervention Type
Procedure
Intervention Name(s)
Muscle biopsy
Intervention Description
muscle biopsy under local anaesthetic taken from the thigh, again for analysis and storage 3 times: before, during and after the exercise programme
Primary Outcome Measure Information:
Title
Assess the feasibility of carrying out a two week preoperative exercise program in patients with colorectal cancer and assess the effects of preoperative exercise on the proliferation of colorectal cancer cells
Description
To assess the feasibility of carrying out a two week preoperative exercise program in patients with colorectal cancer and to assess the effects of preoperative exercise on the proliferation of colorectal cancer cells by measuring the change in the percentage of cells staining positive for Ki67 (a measure of cell proliferation).
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Changes in molecular markers for the effects of exercise and/or diet on AMPK/ mammilian target of rapamycin signalling pathway
Description
Measuring changes in molecular markers for the effects of exercise and/or diet on AMPK/mTOR signalling pathway (phosphorylated 4EBP1 (P4EBP1), phosphorylated protein kinase B (PPKB/AKT), and phosphorylated AMPK (PAMPK).
Time Frame
12 weeks
Title
Changes in AKT expression normal colonic tissue
Description
Measuring changes in AKT expression normal colonic tissue - Intensity of AKT1/AKT2 staining, or AKT phosphorylation, a marker of insulin receptor signalling in cells.
Time Frame
12 weeks
Title
Assessing Apoptosis index
Description
Assessing Apoptosis index - Percentage of tumour cells staining positive for DNA fragmentation, a marker of cells undergoing apoptosis and therefore cell death.
Time Frame
12 weeks
Title
Changes in molecular markers that may mediate or modify exercise/dietary effects in tumour tissues
Description
Measuring changes in molecular markers that may mediate or modify exercise/dietary effects in tumour tissues (IR, IGF1R, p53 and its transcriptional target p21, ER, progesterone receptor, tumor necrosis factor-alpha converting enzyme and TIMP3).
Time Frame
12 weeks
Title
Assessing gene expression profiles
Description
Assessing gene expression profiles focusing on gene associated with insulin resistance.
Time Frame
12 weeks
Title
Assessing the 11 gene signature
Description
Assessing the 11 gene signature that help to predict maximal oxygen uptake gain in patients before and after exercise
Time Frame
12 weeks
Title
Blood methylation profiles.
Description
Blood methylation profiles.
Time Frame
12 weeks
Title
Cortisol levels
Description
Cortisol levels to evaluate levels of biological stress.
Time Frame
12 weeks
Title
Postoperative complications up to 30 days postoperatively
Description
Postoperative complications up to 30 days postoperatively
Time Frame
30 days post op
Title
Moderator variables
Description
Moderator variables including state of motivational readiness for exercise, weight change, depression and anxiety
Time Frame
12 weeks
Title
Irisin levels
Description
Irisin levels before and after exercise
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Colorectal cancer confirmed by histology Considered fit for surgery by surgical and anaesthetic team Considered fit for physical activity programme by MDT Age ≥ 18 years BMI ≥ 26 kg/m2 Not pregnant Non obstructing cancer Able to provide written informed consent Patients not having neoadjuvant chemotherapy Exclusion Criteria: Receiving hormone therapy Patients with diabetes Patients currently on either a dietary or exercise programme reflective of the World Cancer Research Fund Guidelines. Cardiac or renal impairment Excessive use of laxatives History of eating disorders Patients with inflammatory bowel disorders/coeliac Strong family history/polyposis (i.e. more than one 1st degree relative <55yrs) Patients with previous or concurrent malignancies
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tamas Hickish, FRCP
Organizational Affiliation
The Royal Bournemouth and Christchurch Hospitals NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Royal Bournemouth Hospital
City
Bournemouth
State/Province
Dorset
ZIP/Postal Code
BH7 7DW
Country
United Kingdom
Facility Name
Poole Hospital
City
Poole
State/Province
Dorset
ZIP/Postal Code
BH15 2JB
Country
United Kingdom

12. IPD Sharing Statement

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