Heart Failure Activity Coach Study (HEALTHY)
Primary Purpose
Physical Inactivity, Heart Failure
Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
activity coach
sham activity coach
Sponsored by

About this trial
This is an interventional other trial for Physical Inactivity
Eligibility Criteria
Inclusion Criteria:
- Diagnosed heart failure
- Equipped with Optilogg
- Physically inactive (screening)
Exclusion Criteria:
- Does not consent to using accelerometer
- Does not consent to home-visit
- Current participation in another study relating to physical activity
- Life-expectancy less than six months
Sites / Locations
- Skiftinge VC
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Control
Intervention
Arm Description
A sham activity coach will be installed on the Optilogg system, slightly changing its appearance.
The activity coach educates the patient about physical activity, offers means of manually tracking physical activity, and provides trends of registered activity. Furthermore, it provides weekly summaries of registered physical activity and provides means of setting goals for the following week.
Outcomes
Primary Outcome Measures
Study design
Analyze the number of patients needed to be screened to find appropriate and willing participants for the study.
Secondary Outcome Measures
Physical activity
Measured with acelerometer, reported as steps per day
Sedentary time
Measured with accelerometer, evaluate if sedentary time has been decreased by 10 minutes or more.
Goal attainment score
At the start of the study, patients will select to goals relating to physical acitvity which they want to achieve. At the end of the study, this attainment will be evaluated on an ordinal scale with five levels, ranging from -2 to 2, and a mean of the two goal attainments is calculated.
Kansas City Cardiomyopathy Questionnaire
Health-related quality of life assessed by Kansas City Cardiomyopathy Questionnaire, a scale between 0 (very poor) to 100 (excellent).
Full Information
NCT ID
NCT05235763
First Posted
January 21, 2022
Last Updated
October 23, 2023
Sponsor
CareLigo AB
Collaborators
Linkoeping University
1. Study Identification
Unique Protocol Identification Number
NCT05235763
Brief Title
Heart Failure Activity Coach Study
Acronym
HEALTHY
Official Title
Heart Failure Activity Coach Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
June 1, 2022 (Actual)
Primary Completion Date
July 30, 2023 (Actual)
Study Completion Date
September 1, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
CareLigo AB
Collaborators
Linkoeping University
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
An application (app) called the activity coach will be tested to see if it can increase physical activity and decrease sedentary behaviuor, as well as increase quality of life and lead to personal goal attainment in physically inactive heart failure (HF) patients. This pilot randomized controlled trial (RCT) will test the study design and recruitment process, as well as outcomes for a future efficacy RCT.
HF-patients equipped with the mHealth-tool Optilogg will be screened for physical inactivity and then recruited and randomized to either have the activity coach app added to their Optilogg or remain with the standard Optilogg. The study will go on for 12 weeks. Weeks 1 and 12 physical activity using an accelerometer will be recorded, as well as health-related quality of life. At the start of the study the patients will list goals relating to physical activity which the wish to attain, and the level of attainment will be evaluated at the end of the study.
The activity coach educated the patient about physical activity, offers means of manually tracking physical activity, and provides trends of registered activity. Furthermore, it provides weekly summaries of registered physical activity and provides means of setting goals for the following week.
Detailed Description
Study design:
---------------- The activity coach is to be developed using a scientific approach based on the Medical Research Council guidelines, including a small pilot (ethical approval Dnr 2020-01444) which is to be published separately.
This is the first step and the second step is the randomized controlled pilot study (pilot-RCT), to be performed in a primary care setting in Sweden (ethical approval Dnr 2021-05366-01). The purpose is to test the newly developed application (app) called the activity coach, to see if it can improve physical activity, health and quality of life in physically inactive hert failure (HF) patients, but more importantly test the study design and recruitment process, as well as outcomes for a future efficacy RCT.
The patients included will already be equipped with the mHealth tool Optilogg, and then screened for physical inactivty through a self-report question (Blomqvist, 2020, ESC Heart Fail, Utility of single-item questions to assess physical inactivity in patients with chronic heart failure), and then randomized to either receive or not receive the activity coach app.
After randomization the patients will be equipped with an accelerometer for one week. The intervention will go on for 12 weeks, and week twelve the patients will once again carry an acceleroemter.
At baseline demographical data will be recorded, as well as data on co-morbidities and pharmacological treatment. Patients will from a pre-specified list select two goals relating to physical activity that they wish to attain. After 12 weeks they will evaluate the subjective goal attainment on a five level ordinal scale ranging from -2 to 2. At weeks 1 and 12 they will also report health related quality of life using the Kansas City Cardiomyopathy Questionnaire.
Intervention
--------------- The Optilogg system is based around a touch screen computer (tablet), and the activity coach app runs on this screen.
During the first week the patient receives specific education about physical activity and HF on the screen After the first week the patient is expected to be motivated to engage in physical activity and a short slideshow on the screen of the activity coach illustrates how the person using the system can manually register physical activity on the tablet interface. The registered activity trends can be viewed on the screen.At the end of every week the user will receive a weekly summary on screen with the option to set a goal for next week. The goal functionality is optional so that anyone who feels negative stress from the goal, can simply select to not have a goal.
All patients will have access to telephone support during office hours for technical assistance with Optilogg and/or the activity coach.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Physical Inactivity, Heart Failure
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Upon recruitment, patients are randomized 1:1 to either intervention or control group. The study arms run in parallell for the twelve weeks.
Masking
Participant
Allocation
Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
A sham activity coach will be installed on the Optilogg system, slightly changing its appearance.
Arm Title
Intervention
Arm Type
Experimental
Arm Description
The activity coach educates the patient about physical activity, offers means of manually tracking physical activity, and provides trends of registered activity. Furthermore, it provides weekly summaries of registered physical activity and provides means of setting goals for the following week.
Intervention Type
Other
Intervention Name(s)
activity coach
Intervention Description
The activity coach educates the patient about physical activity, offers means of manually tracking physical activity, and provides trends of registered activity. Furthermore, it provides weekly summaries of registered physical activity and provides means of setting goals for the following week.
Intervention Type
Other
Intervention Name(s)
sham activity coach
Intervention Description
The visual appearance of Optilogg is changed as to make the patient aware that something has happened to it, hence not knowing if it is the real activity coach or not. No new functionality is added, however.
Primary Outcome Measure Information:
Title
Study design
Description
Analyze the number of patients needed to be screened to find appropriate and willing participants for the study.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Physical activity
Description
Measured with acelerometer, reported as steps per day
Time Frame
12 weeks
Title
Sedentary time
Description
Measured with accelerometer, evaluate if sedentary time has been decreased by 10 minutes or more.
Time Frame
12 weeks
Title
Goal attainment score
Description
At the start of the study, patients will select to goals relating to physical acitvity which they want to achieve. At the end of the study, this attainment will be evaluated on an ordinal scale with five levels, ranging from -2 to 2, and a mean of the two goal attainments is calculated.
Time Frame
12 weeks
Title
Kansas City Cardiomyopathy Questionnaire
Description
Health-related quality of life assessed by Kansas City Cardiomyopathy Questionnaire, a scale between 0 (very poor) to 100 (excellent).
Time Frame
12 weeks
Other Pre-specified Outcome Measures:
Title
System adherence
Description
For the intervention group, analysis of the frequency with which they used the activity coach
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosed heart failure
Equipped with Optilogg
Physically inactive (screening)
Exclusion Criteria:
Does not consent to using accelerometer
Does not consent to home-visit
Current participation in another study relating to physical activity
Life-expectancy less than six months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tiny Jaarsma, PhD
Organizational Affiliation
Linkoeping University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Skiftinge VC
City
Eskilstuna
ZIP/Postal Code
63188
Country
Sweden
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
32372549
Citation
Blomqvist A, Back M, Klompstra L, Stromberg A, Jaarsma T. Utility of single-item questions to assess physical inactivity in patients with chronic heart failure. ESC Heart Fail. 2020 Aug;7(4):1467-1476. doi: 10.1002/ehf2.12709. Epub 2020 May 6.
Results Reference
background
Learn more about this trial
Heart Failure Activity Coach Study
We'll reach out to this number within 24 hrs