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Evidence-Based Lifestyle Prescription Program: Pilot Study (HeSP)

Primary Purpose

Chronic Disease, Sedentary Lifestyle, Overweight

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
HealtheSteps Program
Sponsored by
Western University, Canada
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Chronic Disease focused on measuring lifestyle intervention, physical activity, exercise, eHealth, technology, coaching, healthy eating

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • One or more self-reported or measured risk factors for chronic disease including: a) objectively-measured body-mass index of greater than or equal to 25 kg/m2; b) less than 150 minutes of exercise per week; c) greater than 3 hours of sitting per day; d) less than 8 fruit and vegetable servings per day; e) diagnosis of metabolic syndrome or type 2 diabetes
  • Clear Physical Activity Readiness Questionnaire (PAR-Q) (i.e., either by answering "No" to all questions or receiving clearance from a healthcare provider)

Exclusion Criteria:

  • Unable to comprehend letter of information and consent documentation

Sites / Locations

  • SJHC Family Medical Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

HealtheSteps Program

Usual-care wait-list control

Arm Description

6 month evidence-based lifestyle Rx program: receive lifestyle Rx's for exercise, physical activity (step counts) and healthy eating and set goals around Rx's (in person sessions at set time points during 6-month period); take part in self-directed healthy living activities to achieve Rx's (Months 0-6); access to a suite of health technology support options for additional support and coaching (Months 0-6).

No active intervention (usual care).

Outcomes

Primary Outcome Measures

Average steps per day
Measured over 7-day monitoring period using pedometers (Yamax Digiwalker SW200 model)

Secondary Outcome Measures

Total physical activity (metabolic equivalent (MET)-minutes/week)
From the International Physical Activity Questionnaire - Short Version
Time spent in sedentary activity (minutes/day)
From the International Physical Activity Questionnaire - Short Version
Eating habits: Total healthful eating score
Measured by Starting the conversation questionnaire
Eating habits: Fruit and vegetable consumption
Measured by the modified Dietary Instrument for Nutrition Education questionnaire
Eating habits: Fatty food score
Measured by the modified Dietary Instrument for Nutrition Education questionnaire
Eating habits: sugary food consumption
Measured by the modified Dietary Instrument for Nutrition Education questionnaire
Health-related quality of life: self-rated health
Visual Analogue Scale score measured using questionnaire known as EQ-5D-3L
Resting systolic blood pressure
Measured using automated blood pressure monitor
Resting diastolic blood pressure
Measured using automated blood pressure monitor
Weight loss (absolute and percentage)
Measured using digital weight scale
Waist circumference
Measured using tape measure
Body mass index
Calculated from height (stadiometer) and weight (digital weight scale) measurements

Full Information

First Posted
April 6, 2015
Last Updated
September 27, 2017
Sponsor
Western University, Canada
Collaborators
Public Health Agency of Canada (PHAC)
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1. Study Identification

Unique Protocol Identification Number
NCT02413385
Brief Title
Evidence-Based Lifestyle Prescription Program: Pilot Study
Acronym
HeSP
Official Title
Canadian Diabetes Strategy Research Project - HealtheSteps™: Exercise and Healthy Eating Prescriptions to Reduce the Risk of Diabetes in Rural and Remote Communities: A Pilot Pragmatic Randomized Controlled Trial (Project 3).
Study Type
Interventional

2. Study Status

Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
May 2015 (Actual)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
March 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Western University, Canada
Collaborators
Public Health Agency of Canada (PHAC)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The HealtheSteps™ (HeS) Program is an evidence-based, community-focused, lifestyle prescription (Rx) program, supported by in-person coaching and innovative health technologies. The program improves the health of Canadians and reduces their risk for chronic disease by tackling three major risk factors that are shared across a number of chronic diseases: physical inactivity, sedentary behaviour and poor diet. Each HeS participant receives an individualized healthy living Rx for exercise, physical activity (step counts) and healthy eating, supported by coaching and technology tools to promote long-term health behaviour change. For this study, the investigators will undertake a 6-month pilot pragmatic randomized controlled trial (RCT), conducted within 5 clinic settings in Southwestern Ontario. The primary aim is to conduct an outcome evaluation to determine the effectiveness of the HeS program in helping at-risk individuals increase physical activity levels, improve eating habits, and improve other health behaviours and health indicators.
Detailed Description
The HealtheSteps™ (HeS) program was developed to improve the health of Canadians and reduce their risk for chronic disease (CD) and brings together emerging evidence from the areas of physical activity, nutrition, behaviour change, health technologies, and knowledge transfer, and moves knowledge into practice. HeS is an evidence-based, viable, and scalable healthy lifestyle solution to tackle the epidemic of CD in Canada. HeS goes beyond traditional health promotion messaging to give individuals a specific plan of action to improve their health and provides community settings with hands-on training, and resources from study knowledge brokers (KBs) to facilitate program uptake and sustainability. The investigators suggest that a widely available HeS program has the potential to impact the lives of Canadians at-risk for and living with CD; shift practice patterns within Family Health Teams (FHTs), Community Health Centres (CHCs) and clinics; reduce health care costs associated with CD; and inform policy decisions about health resource allocation and human resource planning. A scaled-up HeS program will offer at-risk Canadians an opportunity to actively participate in an evidence-based, community-focused, affordable (no cost to participant), healthy lifestyle program supported by point-of-care coaching and innovative electronic Health (eHealth) technologies. This study will use a two-arm, pilot pragmatic randomized controlled trial (RCT) design. It will take place within 5 clinic settings in Southwestern Ontario. Following assessment of eligibility and baseline measurements, participants will be individually randomized (1:1; stratified by clinical setting) to either the intervention group (receiving the HeS program) or to the comparison group (usual care wait-list control). The comparison group will be offered to start the HeS program after a 6 month delay. All participants (both intervention and comparison groups) will receive publicly available healthy eating and physical activity materials at baseline. Measurements will be taken at baseline and 6 months in both groups; additional follow-up measurements will be taken in the intervention group only at 12 months and again at 18 months (from baseline). Groups will be compared at 6-months in order to examine effectiveness of the HeS program; further, follow-up to 12 and 18 months will be used to look at maintenance of any changes in the intervention group only.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Disease, Sedentary Lifestyle, Overweight
Keywords
lifestyle intervention, physical activity, exercise, eHealth, technology, coaching, healthy eating

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
118 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HealtheSteps Program
Arm Type
Experimental
Arm Description
6 month evidence-based lifestyle Rx program: receive lifestyle Rx's for exercise, physical activity (step counts) and healthy eating and set goals around Rx's (in person sessions at set time points during 6-month period); take part in self-directed healthy living activities to achieve Rx's (Months 0-6); access to a suite of health technology support options for additional support and coaching (Months 0-6).
Arm Title
Usual-care wait-list control
Arm Type
No Intervention
Arm Description
No active intervention (usual care).
Intervention Type
Behavioral
Intervention Name(s)
HealtheSteps Program
Intervention Description
6-month evidence-based lifestyle Rx program: At set time points over the 6-month period, participants have in-person visits with a HeS coach at the clinic setting. At each in-person session, the participant receives an individualized Rx for exercise, physical activity (step count) and healthy eating. The HeS Coach and participant then engage in a coaching/goal setting conversation to set detailed plans and goals to achieve their prescriptions. Participants independently choose which activities they will take part in to achieve their lifestyle Rx's and goals. In between in-person sessions, the participants have access to a suite of free-of-charge health technology support tools to: a) track their exercise, physical activity, and healthy eating; and b) receive virtual coaching and support.
Primary Outcome Measure Information:
Title
Average steps per day
Description
Measured over 7-day monitoring period using pedometers (Yamax Digiwalker SW200 model)
Time Frame
6 months (plus 12 and 18 months in the intervention group only)
Secondary Outcome Measure Information:
Title
Total physical activity (metabolic equivalent (MET)-minutes/week)
Description
From the International Physical Activity Questionnaire - Short Version
Time Frame
6 months (plus 12 and 18 months in the intervention group only)
Title
Time spent in sedentary activity (minutes/day)
Description
From the International Physical Activity Questionnaire - Short Version
Time Frame
6 months (plus 12 and 18 months in the intervention group only)
Title
Eating habits: Total healthful eating score
Description
Measured by Starting the conversation questionnaire
Time Frame
6 months (plus 12 and 18 months in the intervention group only)
Title
Eating habits: Fruit and vegetable consumption
Description
Measured by the modified Dietary Instrument for Nutrition Education questionnaire
Time Frame
6 months (plus 12 and 18 months in the intervention group only)
Title
Eating habits: Fatty food score
Description
Measured by the modified Dietary Instrument for Nutrition Education questionnaire
Time Frame
6 months (plus 12 and 18 months in the intervention group only)
Title
Eating habits: sugary food consumption
Description
Measured by the modified Dietary Instrument for Nutrition Education questionnaire
Time Frame
6 months (plus 12 and 18 months in the intervention group only)
Title
Health-related quality of life: self-rated health
Description
Visual Analogue Scale score measured using questionnaire known as EQ-5D-3L
Time Frame
6 months (plus 12 and 18 months in the intervention group only)
Title
Resting systolic blood pressure
Description
Measured using automated blood pressure monitor
Time Frame
6 months (plus 12 and 18 months in the intervention group only)
Title
Resting diastolic blood pressure
Description
Measured using automated blood pressure monitor
Time Frame
6 months (plus 12 and 18 months in the intervention group only)
Title
Weight loss (absolute and percentage)
Description
Measured using digital weight scale
Time Frame
6 months (plus 12 and 18 months in the intervention group only)
Title
Waist circumference
Description
Measured using tape measure
Time Frame
6 months (plus 12 and 18 months in the intervention group only)
Title
Body mass index
Description
Calculated from height (stadiometer) and weight (digital weight scale) measurements
Time Frame
6 months (plus 12 and 18 months in the intervention group only)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: One or more self-reported or measured risk factors for chronic disease including: a) objectively-measured body-mass index of greater than or equal to 25 kg/m2; b) less than 150 minutes of exercise per week; c) greater than 3 hours of sitting per day; d) less than 8 fruit and vegetable servings per day; e) diagnosis of metabolic syndrome or type 2 diabetes Clear Physical Activity Readiness Questionnaire (PAR-Q) (i.e., either by answering "No" to all questions or receiving clearance from a healthcare provider) Exclusion Criteria: Unable to comprehend letter of information and consent documentation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert J Petrella, MD, PhD
Organizational Affiliation
University of Western Ontario, Lawson Health Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
SJHC Family Medical Centre
City
London
State/Province
Ontario
ZIP/Postal Code
N6G 1J1
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
12726869
Citation
Petrella RJ, Koval JJ, Cunningham DA, Paterson DH. Can primary care doctors prescribe exercise to improve fitness? The Step Test Exercise Prescription (STEP) project. Am J Prev Med. 2003 May;24(4):316-22. doi: 10.1016/s0749-3797(03)00022-9.
Results Reference
background
PubMed Identifier
15735210
Citation
Petrella RJ, Lattanzio CN, Demeray A, Varallo V, Blore R. Can adoption of regular exercise later in life prevent metabolic risk for cardiovascular disease? Diabetes Care. 2005 Mar;28(3):694-701. doi: 10.2337/diacare.28.3.694.
Results Reference
background
PubMed Identifier
17846397
Citation
Petrella RJ, Lattanzio CN, Overend TJ. Physical activity counseling and prescription among canadian primary care physicians. Arch Intern Med. 2007 Sep 10;167(16):1774-81. doi: 10.1001/archinte.167.16.1774.
Results Reference
background
PubMed Identifier
20463260
Citation
Petrella RJ, Lattanzio CN, Shapiro S, Overend T. Improving aerobic fitness in older adults: effects of a physician-based exercise counseling and prescription program. Can Fam Physician. 2010 May;56(5):e191-200.
Results Reference
background
PubMed Identifier
21324150
Citation
Petrella RJ, Aizawa K, Shoemaker K, Overend T, Piche L, Marin M, Shapiro S, Atkin S. Efficacy of a family practice-based lifestyle intervention program to increase physical activity and reduce clinical and physiological markers of vascular health in patients with high normal blood pressure and/or high normal blood glucose (SNAC): study protocol for a randomized controlled trial. Trials. 2011 Feb 16;12:45. doi: 10.1186/1745-6215-12-45.
Results Reference
background
PubMed Identifier
21880237
Citation
Stuckey M, Fulkerson R, Read E, Russell-Minda E, Munoz C, Kleinstiver P, Petrella R. Remote monitoring technologies for the prevention of metabolic syndrome: the Diabetes and Technology for Increased Activity (DaTA) study. J Diabetes Sci Technol. 2011 Jul 1;5(4):936-44. doi: 10.1177/193229681100500417.
Results Reference
background
PubMed Identifier
21880236
Citation
Stuckey M, Russell-Minda E, Read E, Munoz C, Shoemaker K, Kleinstiver P, Petrella R. Diabetes and Technology for Increased Activity (DaTA) study: results of a remote monitoring intervention for prevention of metabolic syndrome. J Diabetes Sci Technol. 2011 Jul 1;5(4):928-35. doi: 10.1177/193229681100500416.
Results Reference
background
PubMed Identifier
24500553
Citation
Noble E, Melling J, Shoemaker K, Tikkanen H, Peltonen J, Stuckey M, Petrella RJ. Innovation to reduce cardiovascular complications of diabetes at the intersection of discovery, prevention and knowledge exchange. Can J Diabetes. 2013 Oct;37(5):282-93. doi: 10.1016/j.jcjd.2013.07.061.
Results Reference
background
PubMed Identifier
18179688
Citation
Kitson AL, Rycroft-Malone J, Harvey G, McCormack B, Seers K, Titchen A. Evaluating the successful implementation of evidence into practice using the PARiHS framework: theoretical and practical challenges. Implement Sci. 2008 Jan 7;3:1. doi: 10.1186/1748-5908-3-1.
Results Reference
background
PubMed Identifier
12068568
Citation
Rycroft-Malone J, Harvey G, Kitson A, McCormack B, Seers K, Titchen A. Getting evidence into practice: ingredients for change. Nurs Stand. 2002 May 29-Jun 4;16(37):38-43. doi: 10.7748/ns2002.05.16.37.38.c3201.
Results Reference
background
PubMed Identifier
21258626
Citation
Ward V, House A, Hamer S. Knowledge Brokering: The missing link in the evidence to action chain? Evid Policy. 2009 Aug;5(3):267-279. doi: 10.1332/174426409X463811.
Results Reference
background
PubMed Identifier
31253112
Citation
Gill DP, Blunt W, Boa Sorte Silva NC, Stiller-Moldovan C, Zou GY, Petrella RJ. The HealtheSteps lifestyle prescription program to improve physical activity and modifiable risk factors for chronic disease: a pragmatic randomized controlled trial. BMC Public Health. 2019 Jun 28;19(1):841. doi: 10.1186/s12889-019-7141-2.
Results Reference
derived
PubMed Identifier
28173782
Citation
Gill DP, Blunt W, Bartol C, Pulford RW, De Cruz A, Simmavong PK, Gavarkovs A, Newhouse I, Pearson E, Ostenfeldt B, Law B, Karvinen K, Moffit P, Jones G, Watson C, Zou G, Petrella RJ. HealtheSteps Study Protocol: a pragmatic randomized controlled trial promoting active living and healthy lifestyles in at-risk Canadian adults delivered in primary care and community-based clinics. BMC Public Health. 2017 Feb 7;17(1):173. doi: 10.1186/s12889-017-4047-8.
Results Reference
derived
Links:
URL
http://www.healthesteps.ca
Description
Improving the health of Canadians with evidence-based lifestyle prescriptions website

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Evidence-Based Lifestyle Prescription Program: Pilot Study

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