Lifestyle Intervention Among Participants of the French Colorectal Cancer Screening Program (LIFE-SCREEN)
Primary Purpose
Colorectal Cancer
Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Diet and lifestyle advice following a positive FIT test and diagnostic colonoscopy.
Sponsored by
About this trial
This is an interventional prevention trial for Colorectal Cancer focused on measuring colorectal cancer, prevention
Eligibility Criteria
Inclusion Criteria:
- At high risk for CRC but CRC negative (confirmed by colonoscopy)
- Able to provide informed consent
- Understanding and able to speak French
Exclusion Criteria:
- Extensive intestinal surgery such as colectomy or surgical resection of the colon
- Chronic gastrointestinal illness (inflammatory bowel disease (IBD), irritable bowel syndrome (IBS), celiac disease)
- Use of any systemic antibiotics, antifungals, antivirals, or antiparasitics in the past 3 months
- Use of probiotic medications in the past 3 months
- Under a strict diet such as meal replacements, diets for co-morbidities such as diabetes
- Immobile due to physical constraints (e.g. handicap that is not compatible with physical activities)
Sites / Locations
- International Agency for Research on CancerRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
Intervention
Control
Arm Description
Colorectal cancer free participants receive evidence-based diet and lifestyle advice in addition to the 'usual care' following a positive FIT test and diagnostic colonoscopy
Colorectal cancer free participants receive the 'usual care' following a positive FIT test and diagnostic colonoscopy
Outcomes
Primary Outcome Measures
Change in knowledge score assessed via a knowledge questionnaire
The knowledge regarding the effect of lifestyle factors on cancer risk and cancer prevention lifestyle recommendations will be assessed via a knowledge score derived from the General Nutrition & Physical Activity Knowledge Questionnaires
Improvement in lifestyle score assessed via lifestyle questionnaires
WCRF lifestyle score will be assessed through lifestyle questionnaires. Compliance with the WCRF recommendations is considered achieved if this WCRF lifestyle score increases to more than 5 out of 8.
The following questionnaires will be used to assess lifestyle changes:
French EPIC food frequency questionnaire; the International Physical Activity Questionnaires - IPAQ; Weight and height measurements to assess BMI.
Secondary Outcome Measures
Full Information
NCT ID
NCT04257526
First Posted
August 30, 2019
Last Updated
October 2, 2023
Sponsor
International Agency for Research on Cancer
Collaborators
Centre Leon Berard, Hôpital Edouard Herriot, University of Bordeaux
1. Study Identification
Unique Protocol Identification Number
NCT04257526
Brief Title
Lifestyle Intervention Among Participants of the French Colorectal Cancer Screening Program
Acronym
LIFE-SCREEN
Official Title
Development and Evaluation of a Lifestyle Intervention Among Participants of the French Colorectal Cancer Screening Program
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 23, 2022 (Actual)
Primary Completion Date
May 31, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
International Agency for Research on Cancer
Collaborators
Centre Leon Berard, Hôpital Edouard Herriot, University of Bordeaux
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The investigators propose a randomized controlled trial to develop and evaluate the impact of promoting advice on diet and lifestyle recommendations for cancer prevention at colorectal cancer screening among individuals who may be at higher risk for colorectal cancer (CRC). The specific objectives of this study are to 1) develop a lifestyle intervention based on evidenced-based diet and lifestyle recommendations (i.e. those proposed by the World Cancer Research Fund (WCRF) and the French National Cancer Institute); 2) evaluate the effect of the intervention on the adherence to the target diet and lifestyle recommendations as well as other subjective health measures, including quality of life; 3) evaluate the effect of the intervention on biological pathways linked to colorectal cancer development including physical fitness, anthropometrics, biomarkers for nutrition, and metabolic health.
Detailed Description
This study will be a parallel, two-arm, randomized controlled trial (RCT) in individuals at higher risk of colorectal cancer (CRC), comparing an evidence-based diet and lifestyle advice intervention with 'usual care'. Participants will be recruited during CRC screening and will be included if they have a positive faecal immunochemical test (FIT) and are diagnosed with adenomas but are CRC negative during the colonoscopy. The advice provided will be developed based on the World Cancer Research Fund (WCRF) & French National Cancer Institute (INCA) evidence-based diet and lifestyle recommendations using the habit-theory and will be delivered using multiple materials (e.g. leaflets, posters and digital information) by health professionals in hospitals based in the Rhone region, France. Invitation to participate in the trial will be performed by the gastroenterologist during the clinical visit to provide information on colonoscopy, but the delivery of the intervention and baseline measurement will happen two to three weeks after the colonoscopy. Data will be collected at baseline, 3, 6 and 12 months. At baseline, participants will be required to answer questionnaires on sociodemographic and medical history. At all aforementioned time points, online or paper-based questionnaires will be administered to collect information on diet and lifestyle behaviours, knowledge on healthy lifestyle, quality of life and medical therapy. Participants will also have their anthropometric measures and physical fitness test taken and blood, faecal and colon tissue samples collected during baseline and follow-up appointments (tissue samples will be obtained only for those who are required to undergo the colonoscopy again at 12 months as part of the screening programme). The primary outcome of this intervention will be adherence to target recommendations at 3 months and beyond. Univariate and multivariate statistical analyses as well as qualitative analyses will be performed.
Providing lifestyle advice for cancer prevention at screening programs is a new field in public health that has the potential to be cost-effective, convenient, appealing and wide-reaching. It may also help to reach individuals at higher risk at a time-window when they are more receptive to advice on healthy lifestyles and more likely to make the required behavioural changes. The proposed intervention is expected to have a positive impact on adherence to cancer prevention recommendations, as well as on quality of life, biomarkers for cancer risk, physical fitness and body weight among individuals at higher risk of CRC.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
colorectal cancer, prevention
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
500 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Active Comparator
Arm Description
Colorectal cancer free participants receive evidence-based diet and lifestyle advice in addition to the 'usual care' following a positive FIT test and diagnostic colonoscopy
Arm Title
Control
Arm Type
No Intervention
Arm Description
Colorectal cancer free participants receive the 'usual care' following a positive FIT test and diagnostic colonoscopy
Intervention Type
Behavioral
Intervention Name(s)
Diet and lifestyle advice following a positive FIT test and diagnostic colonoscopy.
Intervention Description
Participants will be recruited during CRC screening and will be included if they have a positive faecal immunochemical test (FIT) and are diagnosed with adenomas but are CRC negative during the colonoscopy. Participants receive evidence-based diet and lifestyle advice intervention with 'usual care'.
Primary Outcome Measure Information:
Title
Change in knowledge score assessed via a knowledge questionnaire
Description
The knowledge regarding the effect of lifestyle factors on cancer risk and cancer prevention lifestyle recommendations will be assessed via a knowledge score derived from the General Nutrition & Physical Activity Knowledge Questionnaires
Time Frame
1 year
Title
Improvement in lifestyle score assessed via lifestyle questionnaires
Description
WCRF lifestyle score will be assessed through lifestyle questionnaires. Compliance with the WCRF recommendations is considered achieved if this WCRF lifestyle score increases to more than 5 out of 8.
The following questionnaires will be used to assess lifestyle changes:
French EPIC food frequency questionnaire; the International Physical Activity Questionnaires - IPAQ; Weight and height measurements to assess BMI.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
At high risk for CRC but CRC negative (confirmed by colonoscopy)
Able to provide informed consent
Understanding and able to speak French
Exclusion Criteria:
Extensive intestinal surgery such as colectomy or surgical resection of the colon
Chronic gastrointestinal illness (inflammatory bowel disease (IBD), irritable bowel syndrome (IBS), celiac disease)
Use of any systemic antibiotics, antifungals, antivirals, or antiparasitics in the past 3 months
Use of probiotic medications in the past 3 months
Under a strict diet such as meal replacements, diets for co-morbidities such as diabetes
Immobile due to physical constraints (e.g. handicap that is not compatible with physical activities)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marc J Gunter, PhD
Phone
0033472738093
Email
GunterM@iarc.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Inge Huybrechts, PhD
Phone
0033472738148
Email
HuybrechtsI@iarc.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marc J Gunter, PhD
Organizational Affiliation
International Agency for Research on Cancer
Official's Role
Principal Investigator
Facility Information:
Facility Name
International Agency for Research on Cancer
City
Lyon
State/Province
Rhone
ZIP/Postal Code
69008
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marc J Gunter, PhD
Phone
0033472738093
Email
GunterM@iarc.fr
First Name & Middle Initial & Last Name & Degree
Inge Huybrechts, PhD
Phone
0033472738148
Email
HuybrechtsI@iarc.fr
First Name & Middle Initial & Last Name & Degree
Nathalie Kliemann, PhD
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Lifestyle Intervention Among Participants of the French Colorectal Cancer Screening Program
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