search
Back to results

Healthy Eating and Active Lifestyle After Bowel Cancer: HEAL ABC (HEALABC)

Primary Purpose

Colorectal Cancer, Survivorship, Behavior, Health

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
HEAL ABC
Sponsored by
University of Manchester
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Colorectal Cancer focused on measuring colorectal, cancer, diet, physical activity, survivorship, behaviour

Eligibility Criteria

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

Inclusion Criteria:

  • Adults, age ≥18
  • Minimum 12 weeks post-surgery and/or active treatment
  • Completed all active anti-cancer treatments, including surgery, radiotherapy or chemotherapy
  • Body mass index ≥20 kg/m2 and no previous unintentional weight loss ≥5% of body weight in the previous six months.
  • Identified as living an unhealthy lifestyle based on current recommendations - follow less than four of the WCRF/AICR recommendations on eligibility questionnaire
  • Ability to work with computer, smart phone or tablet.
  • Able to give informed consent.

Exclusion Criteria:

  • Receiving treatment for malignancy.
  • Secondary malignancy.
  • Having short bowel syndrome, Crohn's disease, ulcerative colitis, diverticulitis or jejunostomy (due to requirement for a very specific diet).
  • Previous stroke, congested cardiac failure or oedema.
  • Hepatic or renal failure
  • Less than 12 weeks post-surgery or active treatment.
  • Meeting the requirements of a healthy lifestyle (follow four or more of the WCRF/AICR recommendations).
  • Being on any therapeutic diets, multiple food intolerances or allergies.
  • Unplanned weight loss of ≥10% in the previous 3-6 months.
  • Cannot read or communicate in English (due to resource constraints of this PhD study).

Sites / Locations

  • Salford Royal NHS Foundation Trust
  • Manchester University NHS Foundation Trust
  • The University of Manchester

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

HEAL ABC

HEALTH

Arm Description

Participants allocated to the intervention will be encouraged to follow the HEAL ABC resources in order to make a healthy eating and active lifestyle change. This will be achieved by setting specific goal(s) and by making concrete plan(s) to implement changes in their everyday life. Interventions will be delivered in the form of written resources that will guide participants. Supportive phone calls using motivational interviewing techniques will be provided to participants every two weeks to encourage lifestyle changes.

Participants allocated to the control group will be referred to publicly available resources on healthy lifestyle recommendations but will not receive any additional support.

Outcomes

Primary Outcome Measures

Adherence to intervention
Assessed as adherence to WCRF/AICR guidelines by using a scoring system for nutrition and physical activity guideline adherence developed by McCullough and colleagues. Number of goals set and number of changes implemented in everyday life during the 3 months intervention.
Adherence to intervention
Assessed as adherence to WCRF/AICR guidelines by using a scoring system for nutrition and physical activity guideline adherence developed by McCullough and colleagues. Number of goals set and number of changes implemented in everyday life during the 6 months follow up.
Recruitment rates
Cumulative recruitment against target rate each month.
Recruitment rates
Cumulative recruitment against target rate each month.
Retention rates
Calculated as the number of participants who completed the study divided by the number of participants randomised.
Retention rates
Calculated as the number of participants who completed the study divided by the number of participants randomised.
Acceptability of the intervention
This will be qualitatively assessed through in depth interviews with a subset of the trial participants.
Acceptability of the intervention
This will be qualitatively assessed through in depth interviews with a subset of the trial participants.
Data completion rates
Completeness of collected data will be assessed for all time points (% missing).
Data completion rates
Completeness of collected data will be assessed for all time points (% missing).

Secondary Outcome Measures

Change in participants' experience, motivation, barriers and facilitators to use HEAL ABC resources and follow the intervention
Qualitatively assessed with in depth interviews.
Change in behaviour
The health action process approach (HAPA) questionnaires, previously used in publications investigating changes in HAPA constructs in lifestyle interventions. A 5 point Likert scale will be used for each question. Minimum score is 15 and maximum score is 75. Higher score is better score.
Change in dietary intake
Three day dietary assessment. Participants will complete prospectively food diary during the day and enter all foods and drinks consumed into online system for dietary assessment - INTAKE24.
Change in BMI
Body weight [kg] and height [m] to calculate body mass index
Change in waist to hip ratio
waist circumference [cm] and hip circumference [cm] to calculate waist to hip ratio
Change in body composition (BIA)
lean mass [%] and fat mass [%] using bio-impedance machine
Change in body composition (CT scan)
muscle mass [cm2] and fat mass [cm2]using CT scans body composition analysis
Change in physical activity
Global Physical Activity Questionnaire is used to assess the metabolic equivalent (MET) based on Global Physical Activity Questionnaire Analysis Guide: https://www.who.int/ncds/surveillance/steps/resources/GPAQ_Analysis_Guide.pdf
Change in step count
pedometer
Patients' socio-demographic characteristics
age, gender, marital status, occupation, education, income, ethnicity, smoking status and number of supplements used
Contact with primary and secondary healthcare services
The Healthcare Resource Use Questionnaire - questionnaire was developed by a health economist for the EU funded project 'PreventIT' (2016-2018, grant number 689238) responding to the Horizon 2020, Personalised Health and Care call PHC-21: Advancing active and healthy aging with ICT: Early risk detection and intervention. There is no set score - questionnaire is used to estimate the costs associated with different healthcare services used.
Mortality
Patient's medical records
Morbidity
Patient's medical records
Change in Quality of life
SF-12 questionnaire - 12 questions, total score can range from 0 to 100 (sore zero indicates the lowest level of health and 100 indicates the highest level of health).

Full Information

First Posted
December 9, 2019
Last Updated
October 11, 2022
Sponsor
University of Manchester
search

1. Study Identification

Unique Protocol Identification Number
NCT04227353
Brief Title
Healthy Eating and Active Lifestyle After Bowel Cancer: HEAL ABC
Acronym
HEALABC
Official Title
Healthy Eating and Active Lifestyle After Bowel Cancer - HEAL ABC Workbook: Development and Feasibility Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
January 30, 2021 (Actual)
Primary Completion Date
September 30, 2022 (Actual)
Study Completion Date
September 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Manchester

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
Trial Design: This is a feasibility randomised controlled trial. Aim: The study aims to test the Healthy Eating and Active Lifestyle After Bowel Cancer - HEAL ABC intervention and HEAL ABC resources for feasibility and will inform a future definitive randomised controlled trial (RCT). Objectives: Is it practical to run HEAL ABC study as a definitive randomised controlled trial? Adherence to intervention, motivations, barriers and facilitators of CRC survivors to follow HEAL ABC. Study Population: Colorectal cancer survivors who completed surgery and/or active treatment. Intervention: The intervention group will use HEAL ABC resource with supportive telephone calls every two weeks during the intervention period and once a month during the follow up period. Control: Participants follow standard care recommendations. Timing and duration: 3 months intervention with 6 months follow up period
Detailed Description
Background: Investigators were awarded a grant to develop a lifestyle resource called HEAL ABC - the Healthy Eating and Active Lifestyle After Bowel Cancer. This resource is based on prevention guidelines of World Cancer Research Fund and American Institute of Cancer Research. The resource was developed in cooperation with a psychologist and so has incorporated behaviour change theory. Investigators organised focused groups with patients and healthcare professionals, and amended the resource based on their feedback. In this study, investigators will test the HEAL ABC resource and the HEAL ABC intervention for its practicality before further studies will be conducted. HEAL ABC consists of 10 booklets and supportive materials. The order for using the booklets is not specified. Participants will be assigned their first booklet based on the one they perceive to be the easiest for setting an incremental goal and achieving it. This means the participant starts with the booklet of the highest self-efficacy and after the participant achieves successful behaviour change, he or she can move more confidently to the next booklet. During the follow up period, participants will use the follow up booklet which helps them to continue with changes they have made and encourage them to set a new goals. Participants in the intervention group will receive a supportive telephone call every two weeks during the intervention period (three months) and once a month during the six months follow up. Participants allocated to the control group will given information about publicly available resources on healthy lifestyle recommendations. No additional support will be provided. Primary Question/Objective: Is it feasible to run a definitive RCT to determine the effectiveness of HEAL ABC? This study will address questions around suitability and practicality of using the HEAL ABC resource and the ability to run an intervention in relation to adherence, recruitment, retention rates and the ability to collect relevant data. Secondary Question/Objective: Adherence to intervention and the motivations, barriers and facilitators of CRC survivors to follow HEAL ABC.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer, Survivorship, Behavior, Health
Keywords
colorectal, cancer, diet, physical activity, survivorship, behaviour

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study is prospective randomised controlled trial, open label, exploratory/feasibility trial. The study aims to test the Healthy Eating and Active Lifestyle After Bowel Cancer - HEAL ABC intervention and HEAL ABC resources for feasibility and will inform a future definitive randomised controlled trial.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
35 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HEAL ABC
Arm Type
Experimental
Arm Description
Participants allocated to the intervention will be encouraged to follow the HEAL ABC resources in order to make a healthy eating and active lifestyle change. This will be achieved by setting specific goal(s) and by making concrete plan(s) to implement changes in their everyday life. Interventions will be delivered in the form of written resources that will guide participants. Supportive phone calls using motivational interviewing techniques will be provided to participants every two weeks to encourage lifestyle changes.
Arm Title
HEALTH
Arm Type
No Intervention
Arm Description
Participants allocated to the control group will be referred to publicly available resources on healthy lifestyle recommendations but will not receive any additional support.
Intervention Type
Behavioral
Intervention Name(s)
HEAL ABC
Intervention Description
Participants will be assigned their first booklet based on the one they perceive to be the easiest for setting an incremental goal and achieving it. After the participant achieves successful behaviour change, he or she can move more confidently to the next booklet. Support will be provided every two weeks over the phone for 12 weeks. During the follow-up period, participants will use the follow-up booklet which helps them to continue with changes they have made and encourage them to set new goals.
Primary Outcome Measure Information:
Title
Adherence to intervention
Description
Assessed as adherence to WCRF/AICR guidelines by using a scoring system for nutrition and physical activity guideline adherence developed by McCullough and colleagues. Number of goals set and number of changes implemented in everyday life during the 3 months intervention.
Time Frame
3 months
Title
Adherence to intervention
Description
Assessed as adherence to WCRF/AICR guidelines by using a scoring system for nutrition and physical activity guideline adherence developed by McCullough and colleagues. Number of goals set and number of changes implemented in everyday life during the 6 months follow up.
Time Frame
6 months
Title
Recruitment rates
Description
Cumulative recruitment against target rate each month.
Time Frame
3 months
Title
Recruitment rates
Description
Cumulative recruitment against target rate each month.
Time Frame
6 months
Title
Retention rates
Description
Calculated as the number of participants who completed the study divided by the number of participants randomised.
Time Frame
3 months
Title
Retention rates
Description
Calculated as the number of participants who completed the study divided by the number of participants randomised.
Time Frame
6 months
Title
Acceptability of the intervention
Description
This will be qualitatively assessed through in depth interviews with a subset of the trial participants.
Time Frame
3 months
Title
Acceptability of the intervention
Description
This will be qualitatively assessed through in depth interviews with a subset of the trial participants.
Time Frame
6 months
Title
Data completion rates
Description
Completeness of collected data will be assessed for all time points (% missing).
Time Frame
3 months
Title
Data completion rates
Description
Completeness of collected data will be assessed for all time points (% missing).
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Change in participants' experience, motivation, barriers and facilitators to use HEAL ABC resources and follow the intervention
Description
Qualitatively assessed with in depth interviews.
Time Frame
3 months and 6 months
Title
Change in behaviour
Description
The health action process approach (HAPA) questionnaires, previously used in publications investigating changes in HAPA constructs in lifestyle interventions. A 5 point Likert scale will be used for each question. Minimum score is 15 and maximum score is 75. Higher score is better score.
Time Frame
Baseline, 3 months and 6 months
Title
Change in dietary intake
Description
Three day dietary assessment. Participants will complete prospectively food diary during the day and enter all foods and drinks consumed into online system for dietary assessment - INTAKE24.
Time Frame
Baseline, 3 months and 6 months
Title
Change in BMI
Description
Body weight [kg] and height [m] to calculate body mass index
Time Frame
Baseline, 3 months and 6 months
Title
Change in waist to hip ratio
Description
waist circumference [cm] and hip circumference [cm] to calculate waist to hip ratio
Time Frame
Baseline, 3 months and 6 months
Title
Change in body composition (BIA)
Description
lean mass [%] and fat mass [%] using bio-impedance machine
Time Frame
Baseline, 3 months and 6 months
Title
Change in body composition (CT scan)
Description
muscle mass [cm2] and fat mass [cm2]using CT scans body composition analysis
Time Frame
Baseline, 3 months and 6 months
Title
Change in physical activity
Description
Global Physical Activity Questionnaire is used to assess the metabolic equivalent (MET) based on Global Physical Activity Questionnaire Analysis Guide: https://www.who.int/ncds/surveillance/steps/resources/GPAQ_Analysis_Guide.pdf
Time Frame
Baseline, 3 months and 6 months
Title
Change in step count
Description
pedometer
Time Frame
Baseline, 3 months and 6 months
Title
Patients' socio-demographic characteristics
Description
age, gender, marital status, occupation, education, income, ethnicity, smoking status and number of supplements used
Time Frame
Baseline
Title
Contact with primary and secondary healthcare services
Description
The Healthcare Resource Use Questionnaire - questionnaire was developed by a health economist for the EU funded project 'PreventIT' (2016-2018, grant number 689238) responding to the Horizon 2020, Personalised Health and Care call PHC-21: Advancing active and healthy aging with ICT: Early risk detection and intervention. There is no set score - questionnaire is used to estimate the costs associated with different healthcare services used.
Time Frame
6 months
Title
Mortality
Description
Patient's medical records
Time Frame
6 months
Title
Morbidity
Description
Patient's medical records
Time Frame
6 months
Title
Change in Quality of life
Description
SF-12 questionnaire - 12 questions, total score can range from 0 to 100 (sore zero indicates the lowest level of health and 100 indicates the highest level of health).
Time Frame
Baseline, 3 months and 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults, age ≥18 Minimum 12 weeks post-surgery and/or active treatment Completed all active anti-cancer treatments, including surgery, radiotherapy or chemotherapy Body mass index ≥20 kg/m2 and no previous unintentional weight loss ≥5% of body weight in the previous six months. Identified as living an unhealthy lifestyle based on current recommendations - follow less than four of the WCRF/AICR recommendations on eligibility questionnaire Ability to work with computer, smart phone or tablet. Able to give informed consent. Exclusion Criteria: Receiving treatment for malignancy. Secondary malignancy. Having short bowel syndrome, Crohn's disease, ulcerative colitis, diverticulitis or jejunostomy (due to requirement for a very specific diet). Previous stroke, congested cardiac failure or oedema. Hepatic or renal failure Less than 12 weeks post-surgery or active treatment. Meeting the requirements of a healthy lifestyle (follow four or more of the WCRF/AICR recommendations). Being on any therapeutic diets, multiple food intolerances or allergies. Unplanned weight loss of ≥10% in the previous 3-6 months. Cannot read or communicate in English (due to resource constraints of this PhD study).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jana Sremanakova
Organizational Affiliation
University of Manchester
Official's Role
Principal Investigator
Facility Information:
Facility Name
Salford Royal NHS Foundation Trust
City
Manchester
State/Province
Great Manchester
ZIP/Postal Code
M6 8HD
Country
United Kingdom
Facility Name
Manchester University NHS Foundation Trust
City
Manchester
ZIP/Postal Code
M13 9WL
Country
United Kingdom
Facility Name
The University of Manchester
City
Manchester
ZIP/Postal Code
M139PL
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Investigators have published detailed study protocol and will share further details in main study publications
IPD Sharing Time Frame
Study protocol has been published and is available online
IPD Sharing Access Criteria
free access
IPD Sharing URL
https://pilotfeasibilitystudies.biomedcentral.com/articles/10.1186/s40814-020-00721-y
Citations:
PubMed Identifier
31623177
Citation
Sremanakova J, Jones D, Cooke R, Burden S. Exploring Views of Healthcare Professionals, Researchers, and People Living with and beyond Colorectal Cancer on a Healthy-Eating and Active Lifestyle Resource. Nutrients. 2019 Oct 16;11(10):2482. doi: 10.3390/nu11102482.
Results Reference
background
PubMed Identifier
31755089
Citation
Burden S, Jones DJ, Sremanakova J, Sowerbutts AM, Lal S, Pilling M, Todd C. Dietary interventions for adult cancer survivors. Cochrane Database Syst Rev. 2019 Nov 22;2019(11):CD011287. doi: 10.1002/14651858.CD011287.pub2.
Results Reference
background
PubMed Identifier
30563580
Citation
Burden S, Sremanakova J, Jones D, Todd C. Dietary interventions for cancer survivors. Proc Nutr Soc. 2019 Feb;78(1):135-145. doi: 10.1017/S0029665118002690. Epub 2018 Dec 19.
Results Reference
background
PubMed Identifier
28429186
Citation
Wright SJ, Gibson D, Eden M, Lal S, Todd C, Ness A, Burden S. What are colorectal cancer survivors' preferences for dietary advice? A best-worst discrete choice experiment. J Cancer Surviv. 2017 Dec;11(6):782-790. doi: 10.1007/s11764-017-0615-2. Epub 2017 Apr 20.
Results Reference
background
PubMed Identifier
30941834
Citation
Aubrey V, Hon Y, Shaw C, Burden S. Healthy eating interventions in adults living with and beyond colorectal cancer: a systematic review. J Hum Nutr Diet. 2019 Aug;32(4):501-511. doi: 10.1111/jhn.12651. Epub 2019 Apr 3.
Results Reference
background
PubMed Identifier
33292854
Citation
Sremanakova J, Sowerbutts AM, Todd C, Cooke R, Burden S. Healthy Eating and Active Lifestyle After Bowel Cancer (HEAL ABC): feasibility randomised controlled trial protocol. Pilot Feasibility Stud. 2020 Nov 13;6(1):176. doi: 10.1186/s40814-020-00721-y.
Results Reference
derived

Learn more about this trial

Healthy Eating and Active Lifestyle After Bowel Cancer: HEAL ABC

We'll reach out to this number within 24 hrs