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Diet and Physical Activity Intervention in CRC Survivors

Primary Purpose

Colorectal Cancer

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Dietary
Physical activity
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colorectal Cancer focused on measuring colorectal cancer, cancer survivor, western pattern diet, physical activity, behavioral intervention, acceptability, feasibility, randomized controlled trial, compliance

Eligibility Criteria

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

Inclusion Criteria:

  1. Histologically proven colorectal adenocarcinoma;
  2. Within one year of completion of main cancer treatment

Exclusion Criteria:

  1. Persistent/recurrent disease upon recruitment;
  2. Current cancer treatment;
  3. Hereditary CRC syndromes;
  4. Known contraindication to PA;
  5. Illiteracy;
  6. Weekly red/processed meat < 5 servings and daily refined grains < 2 servings
  7. Weekly MPA > 300 minutes

Sites / Locations

  • Pamela Youde Nethersole Eastern HospitalRecruiting
  • Princess Margaret HospitalRecruiting
  • Queen Mary HospitalRecruiting
  • Yan Chai HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

No Intervention

Arm Label

dietary

physical activity

dietary and physical activity

usual care

Arm Description

Dietary intervention to meet the target of 1.<5 servings of red/processed meat weekly; <2 servings would be processed meat 2.2 servings of refined grains daily

Physical activity intervention with the following targets: General health target - 30 minutes of moderate-to-vigorous physical activity (MVPA) 5 days per week (i.e. 10 MET-hours/week); Cancer outcome target - 60 minutes of MVPA 5 days per week (i.e. 18-20 MET-hours/week)

Meeting both the dietary and physical activity targets

Follow the general lifestyle advice in accordance with the recommendations of the Department of Health in Hong Kong available in the public domain

Outcomes

Primary Outcome Measures

Whether the PA and dietary intake targets are met at the end of intervention;
Whether the PA and dietary intake targets are met at the end of intervention; i.e. PA group: achieve PA targets or not Dietary group: achieve dietary target or not PA + dietary group: achieve both PA and dietary targets or not Control group: achieve PA or dietary target or not

Secondary Outcome Measures

Magnitude of change in PA level using objective accelerometry
Magnitude of change in each component of dietary target using validated food frequency questionnaire (FFQ);
Rate and determinants of compliance with intervention;
Rates of compliance - measured by rate of completion of assignment; determinants of compliance measured by a questionnaire
Facilitators and barriers to intervention
Measured by (a) qualitatively during the last group meeting and (b) quantitatively by questionnaire
Measurement of theoretical constructs underlying PA and dietary interventions
Using questionnaire specifically desinged to measure these theoretical constructs
Other possible health benefits arising from the intervention
including Changes in body composition via body mass index (BMI) Changes in body fat and/or visceral fat via waist-hip ratio (WHR) and bioelectrical impedance analysis Physical fitness in the form of submaximal oxygen uptake as predicted by 6-minute ergometry Quality-of-life/mood via validated tools (SF12, FACT, HADS and PSS);
Possible side effects arising from the intervention
including PA-associated injury Dietary deficiency - (i) anaemia (haemoglobin level); (ii) energy and protein deficiency

Full Information

First Posted
October 11, 2012
Last Updated
May 11, 2016
Sponsor
The University of Hong Kong
Collaborators
World Cancer Research Fund International
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1. Study Identification

Unique Protocol Identification Number
NCT01708824
Brief Title
Diet and Physical Activity Intervention in CRC Survivors
Official Title
The Acceptability and Feasibility of a Diet and Physical Activity Intervention to Prevent Recurrence in Colorectal Cancer Survivors: a Phase 2 Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Unknown status
Study Start Date
April 2013 (undefined)
Primary Completion Date
December 2016 (Anticipated)
Study Completion Date
June 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong
Collaborators
World Cancer Research Fund International

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Background - Colorectal cancer (CRC) incidence is increasing at an alarming rate in Hong Kong. A recent report concluded physical activity (PA) protects against colon cancer and foods low in dietary fibre, red meat and processed meat cause CRC. Yet, the influence of lifestyle factors on cancer outcome (i.e. recurrence and survival rates) in CRC survivors is largely unknown. Objectives & hypothesis - Our study aims to evaluate the acceptability of two behavioural interventions for CRC survivors intended to improve cancer outcome and designed to (1) increase PA levels and (2) reduce consumption of a Western diet. The investigators hypothesize that the proposed interventions are (1) efficacious in changing the two targeted behaviours; and (2) acceptable to CRC survivors. Settings and methods - Phase 2 feasibility trial. Two hundred and twenty-four CRC survivors within 12 months of completion of cancer treatment and without evidence of persistent/recurrent disease will be recruited from four public hospitals in Hong Kong after informed consent. Subjects will be randomized in a 2x2 factorial design for the two targeted behaviours prescribed over 12 months. Primary outcome measure is whether the target levels of PA and dietary intake could be met at the end of intervention. Secondary outcome measures include: (1) magnitude of changes in PA level and dietary intakes; (2) rates and determinants of compliance; (3) facilitators and barriers to behavioural change; (4) measurement of theoretical constructs underlying PA and dietary interventions; (5) possible health benefits and side effects (PA-associated injury and nutritional deficiency) arising from the interventions. Outcome will be assessed at baseline, 6 months into intervention and then at 0, 6 and 12 months post-intervention. Impact - If proven feasible, our intervention programme would pave way for a large randomized controlled trial testing the effect of PA and diet on the treatment outcome of CRC.
Detailed Description
Background - Colorectal cancer (CRC) incidence is increasing at an alarming rate in Hong Kong. A recent World Cancer Research Fund (WCRF) report concluded physical activity (PA) protects against colon cancer and foods low in dietary fibre, red meat and processed meat cause CRC. Yet, the influence of lifestyle factors on cancer outcome (i.e. recurrence and survival rates) in CRC survivors is largely unknown. Our literature review showed a paucity of published studies on lifestyle intervention in CRC survivors; none had investigated the effect of such intervention on cancer outcomes. With advances in treatment, CRC survivors live longer. Many of them are motivated to make lifestyle changes. However, our qualitative research has shown a huge service gap in the provision of appropriate PA and dietary advice to CRC survivors. Many patients were unaware of the link between PA and diet with CRC outcome but most demonstrated acceptance of lifestyle intervention. Yet, there is currently no scientifically-based evidence to allow firm recommendations to be made. Objectives & hypothesis - Our study aims to evaluate the acceptability of two behavioural interventions for CRC survivors intended to improve cancer outcome and designed to (1) increase PA levels (to 60 minutes of moderate PA 5 days/week) and (2) reduce consumption of a Western diet (<5 servings of red/processed meat weekly and 2 servings of refined grain daily). We hypothesize that the proposed interventions are (1) efficacious in changing the two targeted behaviours; and (2) acceptable to CRC survivors with compliance rates of about 80%. Settings and methods - The study follows the Medical Research Council Framework for the design and evaluation of complex interventions. Phases 0 and 1 (funded by WCRF) have been completed. This application seeks funding for a Phase 2 feasibility trial. Two hundred and twenty-four CRC survivors within 12 months of completion of cancer treatment and without evidence of persistent/recurrent disease will be recruited from four public hospitals in Hong Kong after informed consent. Subjects will be randomized in a 2x2 factorial design for the two targeted behaviours prescribed over 12 months. Primary outcome measure is whether the target levels of PA and dietary intake could be met at the end of intervention. Secondary outcome measures include: (1) magnitude of changes in PA level and dietary intakes; (2) rates and determinants of compliance by questionnaire; (3) facilitators and barriers to behavioural change by questionnaire; (4) measurement of theoretical constructs underlying PA and dietary interventions by questionnaire; (5) possible health benefits (body composition, physical fitness, quality of life and mood) and side effects (PA-associated injury and nutritional deficiency) arising from the interventions. Outcome will be assessed at baseline, 6 months into intervention and then at 0, 6 and 12 months post-intervention (i.e. at baseline, 6, 12, 18 and 24 months after the start of intervention). Impact - To the best of our knowledge, this is the first behavioural intervention model targeting PA and reduced consumption of a Western diet in CRC survivors. If proven feasible, our intervention programme would pave way for a large randomized controlled trial testing the effect of PA and diet on the treatment outcome 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, cancer survivor, western pattern diet, physical activity, behavioral intervention, acceptability, feasibility, randomized controlled trial, compliance

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
224 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
dietary
Arm Type
Experimental
Arm Description
Dietary intervention to meet the target of 1.<5 servings of red/processed meat weekly; <2 servings would be processed meat 2.2 servings of refined grains daily
Arm Title
physical activity
Arm Type
Experimental
Arm Description
Physical activity intervention with the following targets: General health target - 30 minutes of moderate-to-vigorous physical activity (MVPA) 5 days per week (i.e. 10 MET-hours/week); Cancer outcome target - 60 minutes of MVPA 5 days per week (i.e. 18-20 MET-hours/week)
Arm Title
dietary and physical activity
Arm Type
Experimental
Arm Description
Meeting both the dietary and physical activity targets
Arm Title
usual care
Arm Type
No Intervention
Arm Description
Follow the general lifestyle advice in accordance with the recommendations of the Department of Health in Hong Kong available in the public domain
Intervention Type
Behavioral
Intervention Name(s)
Dietary
Intervention Description
Dietary intervention to meet the target of <5 servings of red/processed meat weekly; <2 servings would be processed meat 2 servings of refined grains daily
Intervention Type
Behavioral
Intervention Name(s)
Physical activity
Intervention Description
Physical activity intervention with the following targets: General health target - 30 minutes of moderate-to-vigorous physical activity (MVPA) 5 days per week (i.e. 10 MET-hours/week); Cancer outcome target - 60 minutes of MVPA 5 days per week (i.e. 18-20 MET-hours/week)
Primary Outcome Measure Information:
Title
Whether the PA and dietary intake targets are met at the end of intervention;
Description
Whether the PA and dietary intake targets are met at the end of intervention; i.e. PA group: achieve PA targets or not Dietary group: achieve dietary target or not PA + dietary group: achieve both PA and dietary targets or not Control group: achieve PA or dietary target or not
Time Frame
at the end of 12 months of intervention
Secondary Outcome Measure Information:
Title
Magnitude of change in PA level using objective accelerometry
Time Frame
6, 12, 18 and 24 months after start of intervention (i.e. interim, 0, 6 and 12 months post-intervention)
Title
Magnitude of change in each component of dietary target using validated food frequency questionnaire (FFQ);
Time Frame
6, 12, 18 and 24 months after start of intervention (i.e. interim, 0, 6 and 12 months post-intervention)
Title
Rate and determinants of compliance with intervention;
Description
Rates of compliance - measured by rate of completion of assignment; determinants of compliance measured by a questionnaire
Time Frame
at the end of 12 months of intervention
Title
Facilitators and barriers to intervention
Description
Measured by (a) qualitatively during the last group meeting and (b) quantitatively by questionnaire
Time Frame
at the end of intervention
Title
Measurement of theoretical constructs underlying PA and dietary interventions
Description
Using questionnaire specifically desinged to measure these theoretical constructs
Time Frame
6, 12, 18 and 24 months after start of intervention (i.e. interim, 0, 6 and 12 months post-intervention)
Title
Other possible health benefits arising from the intervention
Description
including Changes in body composition via body mass index (BMI) Changes in body fat and/or visceral fat via waist-hip ratio (WHR) and bioelectrical impedance analysis Physical fitness in the form of submaximal oxygen uptake as predicted by 6-minute ergometry Quality-of-life/mood via validated tools (SF12, FACT, HADS and PSS);
Time Frame
at 12 and 24 months after start of intervention (i.e. at 0 and 12 months post-intervention)
Title
Possible side effects arising from the intervention
Description
including PA-associated injury Dietary deficiency - (i) anaemia (haemoglobin level); (ii) energy and protein deficiency
Time Frame
at 6, 12, 18 and 24 months after start of intervention (i.e. interim, 0, 6 and 12 months post-intervention)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically proven colorectal adenocarcinoma; Within one year of completion of main cancer treatment Exclusion Criteria: Persistent/recurrent disease upon recruitment; Current cancer treatment; Hereditary CRC syndromes; Known contraindication to PA; Illiteracy; Weekly red/processed meat < 5 servings and daily refined grains < 2 servings Weekly MPA > 300 minutes
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Judy WC Ho, MBBS
Phone
852 2255 4762
Email
judyho@hku.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Judy WC Ho, MBBS
Organizational Affiliation
Queen Mary Hospital, University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pamela Youde Nethersole Eastern Hospital
City
Hong Kong
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hester Cheung, MBBS
Email
cheuys@ha.org.hk
Facility Name
Princess Margaret Hospital
City
Hong Kong
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
SM Hui, MBBS
Email
huism@ha.org.hk
Facility Name
Queen Mary Hospital
City
Hong Kong
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Judy WC Ho, MBBS
Phone
852 2255 4762
Email
judyho@hku.hk
First Name & Middle Initial & Last Name & Degree
Judy WC Ho, MBBS
Facility Name
Yan Chai Hospital
City
Hong Kong
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
CK Kong, MBBS
Email
kck326@ha.org.hk

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
no consent has been obtained to make individual participant data available
Citations:
PubMed Identifier
34433608
Citation
Wong JYH, Ho JWC, Lee AM, Fong DYT, Chu N, Leung S, Chan YYW, Lam SH, Leung IPF, Macfarlane D, Cerin E, Taylor AJ, Cheng KK. Lived experience of dietary change among Chinese colorectal cancer survivors in Hong Kong: A qualitative study. BMJ Open. 2021 Aug 25;11(8):e051052. doi: 10.1136/bmjopen-2021-051052.
Results Reference
derived
PubMed Identifier
32072434
Citation
Ho M, Ho JWC, Fong DYT, Lee CF, Macfarlane DJ, Cerin E, Lee AM, Leung S, Chan WYY, Leung IPF, Lam SHS, Chu N, Taylor AJ, Cheng KK. Effects of dietary and physical activity interventions on generic and cancer-specific health-related quality of life, anxiety, and depression in colorectal cancer survivors: a randomized controlled trial. J Cancer Surviv. 2020 Aug;14(4):424-433. doi: 10.1007/s11764-020-00864-0. Epub 2020 Feb 18.
Results Reference
derived
PubMed Identifier
23688320
Citation
Ho JW, Lee AM, Macfarlane DJ, Fong DY, Leung S, Cerin E, Chan WY, Leung IP, Lam SH, Taylor AJ, Cheng KK. Study protocol for "Moving Bright, Eating Smart"- A phase 2 clinical trial on the acceptability and feasibility of a diet and physical activity intervention to prevent recurrence in colorectal cancer survivors. BMC Public Health. 2013 May 20;13:487. doi: 10.1186/1471-2458-13-487.
Results Reference
derived

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Diet and Physical Activity Intervention in CRC Survivors

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