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Heal-Me Personalized Online Nutrition and Exercise Routines (PiONEeR)

Primary Purpose

Cancer, Lung Diseases, Liver Diseases

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Exercise & Nutrition
Exercise & Nutrition
Sponsored by
University of Alberta
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cancer focused on measuring Exercise, Nutrition, Chronic Disease, Virtual

Eligibility Criteria

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

Inclusion Criteria:

  • ≥ 18 years of age
  • In one of the following 3 disease groups:

    1. Cancer survivor who has completed treatment or is receiving maintenance therapy
    2. Patient who is currently post-transplantation from liver or lung transplantation
    3. Patient with chronic lung disease who may or may not be listed for organ transplantation
  • Previous enrolment in exercise rehabilitation program (i.e. rehabilitation "graduate")
  • Access to an Internet connected device with video and audio capabilities

Exclusion Criteria:

  • Compassionate care
  • Unsafe to participate in a virtual exercise program
  • Unable to provide informed consent

Sites / Locations

  • University of Alberta

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Experimental

Experimental

Arm Label

Standard Care

App-Based, Personnel-Light Care

App-Based, Personnel-Intensive Care

Arm Description

The standard of care response to COVID. Educational materials will be provided to patients via email. The package will include a combination of personalized exercises, and nutrition information for healthy eating. Participants will also receive a Garmin watch to track their activity over the intervention.

An app-based, "personnel-light" approach to virtual care with a focus on support through group-based interactions with the Trainers, Dietitians and other participants. The patient's personalized 12-week home based exercise program will be enabled in the app after a baseline exercise specialist appointment. The 10-week nutrition program will be enabled at week 3 after a virtual dietitian assessment in week 2 (~1 hour). The home programs will auto-progress. Participants will also receive a Garmin watch to track their activity over the intervention.

An app-based, "personnel-intensive" approach to virtual care with support through a combination of group-based interactions with Trainers, Dietitians and other participants, as well as one-on-one support with Exercise Trainers and Dietitians. In addition to Group 2 features, patient interaction with Trainers will be via live group classes AND 1-to-1 sessions: up to seven 1-to-1 consultations with an exercise specialist and three 1-to-1 consultations with a dietitian to review progress and goals and make any necessary modifications to programming. Participants will also receive a Garmin watch to track their activity over the intervention.

Outcomes

Primary Outcome Measures

Lower Extremity Functional Scale (LEFS)
The difference in the pre- vs post-intervention change in LEFS score between groups (score range: 0-80, higher scores indicate higher function)

Secondary Outcome Measures

Upper Extremity Functional Index (UEFI)
The difference in the pre- vs post-intervention change in UEFI score between groups (score range: 0-80, higher scores indicate higher function)
Timed Sit-to-Stand (60 & 30 seconds)
The difference in the pre- vs post-intervention change in # of repetitions completed over the Timed Sit-to-Stand between groups
Timed One-Legged Stance
The difference in the pre- vs post-intervention change in Timed One-Legged Stance between groups
2-Minute Step Test (2MST)
The difference in the pre- vs post-intervention change in the # of steps completed in the 2MST between groups
Sit-and-Reach
The difference in the pre- vs post-intervention change in the sit-and-reach distance between groups
Step Count & Activity Minutes
The difference in the pre- vs post-intervention change in step count and activity minutes (Garmin watch) between groups
Overall Well-Being (The World Health Organization-5 [WHO-5] Well-Being Index)
The difference in the pre- vs post-intervention change in The World Health Organization-5 (WHO-5) Well-Being Index between groups (score range: 0-25, higher scores indicate higher well-being)
Resilience (10-Item Connor Davidson Resilience Scale)
The difference in the pre- vs post-intervention change in resilience, as measures by the 10-Item Connor Davidson Resilience Scale, between groups (score range: 0-40, higher scores indicate higher resilience)
General health-related quality of life (36-Item Short Form Survey [SF-36])
The difference in the pre- vs post-intervention change in health-related quality of life, as measured by the SF-36, between groups (score range: 0-100, higher scores indicate a more favorable health state)
General health-related quality of life (5-Level EQ-5D [EQ-5D-5L])
The difference in the pre- vs post-intervention change in health-related quality of life, as measured by the EQ-5D-5L, between groups (visual analogue score range: 0-100, higher scores indicate a more favorable health state)

Full Information

First Posted
November 30, 2020
Last Updated
October 3, 2022
Sponsor
University of Alberta
Collaborators
Alberta Innovates Health Solutions
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1. Study Identification

Unique Protocol Identification Number
NCT04666558
Brief Title
Heal-Me Personalized Online Nutrition and Exercise Routines
Acronym
PiONEeR
Official Title
Heal-Me PiONEeR (Personalized Online Nutrition and Exercise Routines) - Reconnecting Vulnerable Outpatients With Multidisciplinary Care - a Randomized Controlled Trial Assessing 3 Levels of Online Programming in the Time of COVID
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
November 30, 2020 (Actual)
Primary Completion Date
December 17, 2021 (Actual)
Study Completion Date
August 31, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Alberta
Collaborators
Alberta Innovates Health Solutions

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare 12-weeks of virtual multidisciplinary programming provided at three levels of support intensity to determine impacts on clinical outcomes, acceptability, and cost amongst outpatients with cancer, liver disease, or lung disease. Participants will be randomized to one of three groups: (i) standard care, (ii) a personnel-light app-based intervention, (iii) a personnel-intensive app-based intervention. Participants randomized to standard care will receive exercise and nutrition resources as well as a Garmin watch. Participants in the experimental groups will receive standard care, plus a 12-week multidisciplinary app-based personalized program involving 12 weeks of exercise programming and 10-weeks of nutrition programming. Participants in study group 3 will receive additional one-on-one care. The Research Ethics Board at the University of Alberta has approved this study. The protocol will measure patient-related outcome measures including physical function, quality of life, social isolation, and anxiety, as well as measures of acceptability and cost. 216 participants will take part in this study (n=72 per arm). Analyses: fitness testing and patient-reported outcomes will be administered before and after the intervention. Fitness and patient-reported outcomes will be compared using linear mixed models with random effects. App acceptability will be compared between groups using Chi-Square.
Detailed Description
INTRODUCTION: COVID-19 related social distancing have a profound impact on vulnerable people living with chronic conditions, including cancer and organ failure. Pre-pandemic, many of these patients relied on and benefited from multidisciplinary supports and structured programming to maintain well-being and function. Many of these in-person supports are not currently available, which has disconnected these patients from the care they need to stay well. Virtual modalities are a promising solution that allow multidisciplinary programs (i.e. exercise and nutrition) to continue to deliver support for these patients when social distancing doesn't allow these programs to run in-person. However, it's currently unclear whether virtual programming is acceptable in these populations, and what level of support is best in terms of benefits and costs. The purpose of this study is to compare 12-weeks of virtual multidisciplinary programming provided at three levels of support intensity to determine impacts on clinical outcomes, acceptability, and cost amongst outpatients with cancer, liver disease, or lung disease. OBJECTIVES: As compared to control, assess the impact of a 12-week virtual exercise and nutrition program (delivered at 2 levels of support) on: physical function and mental health outcomes. As compared to the modeled costs of in-person programming, assess the cost of a 12-week virtual exercise and nutrition program (delivered at 2 levels of support). Assess the acceptability of the virtual exercise and nutrition programming to patients and members of the study team who deliver the intervention. METHODS: This is a mixed-methods, 12-week randomized controlled trial with randomization to one of three study groups with increasing virtual multidisciplinary support for outpatients. Participants will include people living with one of the following three chronic conditions: cancer, lung disease, or lung or liver disease (post-transplantation). Group 1 - The standard of care response to COVID. Educational materials will be provided to patients via email. As needed, the package will include a combination of personalized exercises, disease-tailored tips for healthy eating and COVID precautions. Ad hoc telephone or virtual contact with patients will be at the providers' discretion. Group 2 - An app-based, "personnel-light" approach to virtual care with a focus on support through group-based interactions with the Trainers and other participants during live group exercise and nutrition classes (~3/week). The patient's personalized 12-week home based exercise program will be enabled in the app after a baseline exercise specialist appointment and the 10-week nutrition program will be enabled at week 3 after a dietitian assessment in week 2. The home programs will auto-progress. Group 3 - An app-based, "personnel-intensive" approach. In addition to Group 2 features, patient interaction with Trainers will be via live group classes AND 1-to-1 sessions: seven 1-to-1 consultations with an exercise specialist and three 1-to-1 consultations with a dietitian to review progress and goals and make any necessary modifications to programming. OUTCOMES & ANALYSES: All analyses adhere to the intention-to-treat-principle (ITT). Fitness assessments and patient-reported outcomes will be collected at baseline and 12-weeks. Primary and secondary outcomes from these data will be analyzed using linear mixed models with random effects. Adherence and app acceptability (survey) will be compared between groups using the chi-square. Costs of each level of support will be compared with the cost of in-person programming using a publicly funded provincial payer perspective and will be presented in the Net Benefit framework. Interviews will be conducted with participants, caregivers, and program instructors to determine program acceptability and barriers and facilitators. Inductive content analysis will be used to analyze qualitative data.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer, Lung Diseases, Liver Diseases
Keywords
Exercise, Nutrition, Chronic Disease, Virtual

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
216 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard Care
Arm Type
No Intervention
Arm Description
The standard of care response to COVID. Educational materials will be provided to patients via email. The package will include a combination of personalized exercises, and nutrition information for healthy eating. Participants will also receive a Garmin watch to track their activity over the intervention.
Arm Title
App-Based, Personnel-Light Care
Arm Type
Experimental
Arm Description
An app-based, "personnel-light" approach to virtual care with a focus on support through group-based interactions with the Trainers, Dietitians and other participants. The patient's personalized 12-week home based exercise program will be enabled in the app after a baseline exercise specialist appointment. The 10-week nutrition program will be enabled at week 3 after a virtual dietitian assessment in week 2 (~1 hour). The home programs will auto-progress. Participants will also receive a Garmin watch to track their activity over the intervention.
Arm Title
App-Based, Personnel-Intensive Care
Arm Type
Experimental
Arm Description
An app-based, "personnel-intensive" approach to virtual care with support through a combination of group-based interactions with Trainers, Dietitians and other participants, as well as one-on-one support with Exercise Trainers and Dietitians. In addition to Group 2 features, patient interaction with Trainers will be via live group classes AND 1-to-1 sessions: up to seven 1-to-1 consultations with an exercise specialist and three 1-to-1 consultations with a dietitian to review progress and goals and make any necessary modifications to programming. Participants will also receive a Garmin watch to track their activity over the intervention.
Intervention Type
Other
Intervention Name(s)
Exercise & Nutrition
Intervention Description
App-based live group exercise classes, personalized follow-up asynchronous workouts, live group nutrition classes, and protein tracking.
Intervention Type
Other
Intervention Name(s)
Exercise & Nutrition
Intervention Description
App-based live group exercise classes, personalized follow-up asynchronous workouts, live group nutrition classes, and protein tracking. Additional one-one-one exercise and nutrition support is provided too.
Primary Outcome Measure Information:
Title
Lower Extremity Functional Scale (LEFS)
Description
The difference in the pre- vs post-intervention change in LEFS score between groups (score range: 0-80, higher scores indicate higher function)
Time Frame
12 Weeks
Secondary Outcome Measure Information:
Title
Upper Extremity Functional Index (UEFI)
Description
The difference in the pre- vs post-intervention change in UEFI score between groups (score range: 0-80, higher scores indicate higher function)
Time Frame
12 weeks
Title
Timed Sit-to-Stand (60 & 30 seconds)
Description
The difference in the pre- vs post-intervention change in # of repetitions completed over the Timed Sit-to-Stand between groups
Time Frame
12 Weeks
Title
Timed One-Legged Stance
Description
The difference in the pre- vs post-intervention change in Timed One-Legged Stance between groups
Time Frame
12 Weeks
Title
2-Minute Step Test (2MST)
Description
The difference in the pre- vs post-intervention change in the # of steps completed in the 2MST between groups
Time Frame
12 Weeks
Title
Sit-and-Reach
Description
The difference in the pre- vs post-intervention change in the sit-and-reach distance between groups
Time Frame
12 Weeks
Title
Step Count & Activity Minutes
Description
The difference in the pre- vs post-intervention change in step count and activity minutes (Garmin watch) between groups
Time Frame
12 Weeks
Title
Overall Well-Being (The World Health Organization-5 [WHO-5] Well-Being Index)
Description
The difference in the pre- vs post-intervention change in The World Health Organization-5 (WHO-5) Well-Being Index between groups (score range: 0-25, higher scores indicate higher well-being)
Time Frame
12 Weeks
Title
Resilience (10-Item Connor Davidson Resilience Scale)
Description
The difference in the pre- vs post-intervention change in resilience, as measures by the 10-Item Connor Davidson Resilience Scale, between groups (score range: 0-40, higher scores indicate higher resilience)
Time Frame
12 Weeks
Title
General health-related quality of life (36-Item Short Form Survey [SF-36])
Description
The difference in the pre- vs post-intervention change in health-related quality of life, as measured by the SF-36, between groups (score range: 0-100, higher scores indicate a more favorable health state)
Time Frame
12 Weeks
Title
General health-related quality of life (5-Level EQ-5D [EQ-5D-5L])
Description
The difference in the pre- vs post-intervention change in health-related quality of life, as measured by the EQ-5D-5L, between groups (visual analogue score range: 0-100, higher scores indicate a more favorable health state)
Time Frame
12 Weeks
Other Pre-specified Outcome Measures:
Title
Physical activity
Description
The difference in the pre- vs post-intervention change in proportion of "yes" answers to the single-item physical activity questionnaire from pre- to post-intervention between groups
Time Frame
12 Weeks
Title
Sedentary Time (International Sedentary Assessment Tool - ISAT)
Description
The difference in the pre- vs post-intervention change in sedentary time, as self-reported on the ISAT between groups
Time Frame
12 Weeks
Title
Protein Intake
Description
The difference in the pre- vs post-intervention change in protein intake (grams) between groups, based on 3-day food record(s)
Time Frame
12 Weeks
Title
Calorie Intake
Description
The difference in the pre- vs post-intervention change in calorie intake (kilocalories) between groups, based on 3-day food record(s)
Time Frame
12 Weeks
Title
Micronutrient Intake
Description
The difference in the pre- vs post-intervention change in micronutrient intake (milligrams) between groups, based on 3-day food record(s)
Time Frame
12 Weeks
Title
Beliefs and outcome expectations about exercise
Description
The difference in the pre- vs post-intervention change in the 6-item COM-B scale between groups (score range: 0-120, higher scores indicate higher capability, opportunity, motivation)
Time Frame
12 Weeks
Title
Program acceptability (Unified Theory of Acceptance and Use of Technology - UTAUT)
Description
The difference in the pre- vs post-intervention change in the UTAUT scale between groups (score range: 0-92, higher scores indicate higher app acceptance and use)
Time Frame
12 Weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥ 18 years of age In one of the following 3 disease groups: Cancer survivor who has completed treatment or is receiving maintenance therapy Patient who is currently post-transplantation from liver or lung transplantation Patient with chronic lung disease who may or may not be listed for organ transplantation Previous enrolment in exercise rehabilitation program (i.e. rehabilitation "graduate") Access to an Internet connected device with video and audio capabilities Exclusion Criteria: Compassionate care Unsafe to participate in a virtual exercise program Unable to provide informed consent
Facility Information:
Facility Name
University of Alberta
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2G4
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
35569753
Citation
Tandon P, Purdy G, Ismond KP, Cruz C, Etruw E, Suderman K, Hyde A, Stickland M, Spence JC, Lien DC, Bhanji R, Prado CM, Cruz AM, Joy AA, Yaskina M, Round J, Harback K, Padwal R, McNeely ML. Heal-me PiONEer (personalized online nutrition and exercise): An RCT assessing 2 levels of app-based programming in individuals with chronic disease. Contemp Clin Trials. 2022 Jul;118:106791. doi: 10.1016/j.cct.2022.106791. Epub 2022 May 13.
Results Reference
derived
PubMed Identifier
34857190
Citation
Cruz C, Prado CM, Punja S, Tandon P. Use of digital technologies in the nutritional management of catabolism-prone chronic diseases: A rapid review. Clin Nutr ESPEN. 2021 Dec;46:152-166. doi: 10.1016/j.clnesp.2021.10.020. Epub 2021 Nov 1.
Results Reference
derived

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Heal-Me Personalized Online Nutrition and Exercise Routines

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