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Sensor-controlled Digital Game for Heart Failure Self-management

A Pilot Sensor-controlled Digital Gaming Intervention With Real-time Behavior Tracking to Motivate Self-management Behaviors in Older Adults With Heart Failure

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03947983
Enrollment
38
Registered
2019-05-13
Start date
2019-11-12
Completion date
2021-01-30
Last updated
2021-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Keywords

self-management, digital game, sensor

Brief summary

This study evaluates a sensor-controlled digital game (SCDG) to motivate self-management behaviors of weight monitoring and physical activity in older adults with heart failure (HF). Half of the participants will receive the SCDG app and weight monitoring and physical activity sensors and the other half will receive only the weight monitoring and physical activity sensors.

Detailed description

The primary goal of this study is to obtain initial efficacy data and undertake a comprehensive feasibility assessment of a SCDG intervention that synchronizes with a Bluetooth-enabled weight scale and activity tracker to activate game rewards and feedback based on older adult heart failure (HF) participants' real-time weight monitoring and exercise behaviors. The SCDG will involve a narrative, the goal of which is to help an avatar in the game avoid rehospitalization by using game points, earned via the participant's real-time behaviors, in game tasks that help maintain the avatar's optimal HF health status. Real-time behaviors of weight-monitoring and physical activity will be tracked by an off-the-shelf sensors and app (Withings). The data from the Withings sensors will then be routed to our SCDG app. The digital game paired with sensors will enable objective tracking of real-time behaviors such as physical activity, and weight monitoring, and provide personalized, contextually relevant feedback (e.g., reduce fluid intake or call doctor for weight gain) to motivate engagement in and generate habit formation of heart failure related self-management behaviors. The goal of this proposal is to demonstrate the feasibility of the SCDG concept with an optimal number of sensors in a small study so as to lay a foundation for scaling this concept to include more relevant sensors in longer, larger studies. In this study, the initial efficacy of the SCDG intervention for primary outcome of rate of engagement in HF self-management behavior of weight-monitoring and secondary outcomes of physical activity engagement, HF self-management-knowledge, and self-efficacy, HF-functional status, hospitalization, cognitive ability, depression and quality of life will be evaluated. For this study, 44 older adults diagnosed with the New York Heart Association's HF classification I to III from out-patient HF settings in central Texas will be recruited, and randomized to either the SCDG intervention group that will receive sensors tracking weight monitoring and activity and play the SCDG on a mobile smartphone for 12 weeks or a control group that will receive sensors and an app tracking activity and weight monitoring, and standardized written HF educational modules.

Interventions

The SCDG will involve a narrative, the goal of which is to help an avatar in the game avoid rehospitalization by using game points, earned via the participant's real-time behaviors, in game tasks that help maintain the avatar's optimal HF health status. Real-time behaviors of weight-monitoring and physical activity will be tracked by an off-the-shelf sensors and app (Withings). The data from the Withings sensors will then be routed to our SCDG app. The digital game paired with sensors will enable objective tracking of real-time behaviors such as physical activity, and weight monitoring, and provide personalized, contextually relevant feedback (e.g., reduce fluid intake or call doctor for weight gain) to motivate engagement in and generate habit formation of heart failure related self-management behaviors.

BEHAVIORALSensor Only

Real-time behaviors of weight-monitoring and physical activity will be tracked by an off-the-shelf sensors and app (Withings). This group will also be provided with standardized evidence-based HF educational material.However, the data from the Withings sensors will not be routed to the SCDG.

Sponsors

National Institute of Nursing Research (NINR)
CollaboratorNIH
University of Texas at Austin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

Participants will be randomized into two arms of intervention group or control group. The control group will receive only the weight monitoring and physical activity sensors while the intervention group will receive a sensor-controlled digital game (SCDG) app and weight monitoring and physical activity sensors

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 55 years or older * New York Heart Association (NYHA) heart failure classification of I to III that permits minimal physical activity without discomfort * Understand English * Pass a mini-cognitive screen * Score of less than 2 (able to independently walk without using a cane or walker) on the Outcome and Assessment Information Set item for ambulation/locomotion * Ownership of a smartphone or digital tablet

Exclusion criteria

* Severe visual (e.g., legally blind) or tactile (e.g., severe arthritis) impairments that adversely prevent the use of a smartphone or sensor devices * History of renal failure which adversely affects heart failure prognosis * Diagnosis of an end stage or terminal illness (e.g., cancer).

Design outcomes

Primary

MeasureTime frameDescription
Number of Days With Weight-monitoring on Sensor Logs at 6 Weeks6 weeksThis outcome will be measured by collecting number of days with weight-monitoring data. This measure will be collected from sensor logs within the apps for both intervention group (IG) and control group (CG).
Number of Days With Weight-monitoring on Sensor Logs at 12 Weeks12 weeksThis outcome will be measured by collecting number of days with weight-monitoring data. This measure will be collected from sensor logs within the apps for both intervention group (IG) and control group (CG).

Secondary

MeasureTime frameDescription
Mean of Daily Steps on Physical Activity Sensor Logs at 6 Weeks6 weeksThis outcome measure will be measured by calculating the average daily steps at end of 6 weeks. These measures will be collected from sensor logs within the apps for both IG and CG.
Mean of Daily Steps on Physical Activity Sensor Logs at 12 Weeks12 weeksThis outcome measure will be measured by calculating the average daily steps at end of 12 weeks. These measures will be collected from sensor logs within the apps for both IG and CG.
Change From Baseline in Heart Failure Self-management Behaviors as Measured by the European Heart Failure Self-care Behavior Scale at 6 WeeksBaseline, 6 weeksThe instrument used will be 9-item European Heart Failure Self-care Behavior Scale (HSBS; standardized score from 0 to 100 (every item is given an equal weight) with a higher score meaning better self-care). Items are on a Likert scale of 1 - 5. For calculating the standardized score, each item is reverse coded and then computed using the formula: (Sum of all ever-coded items - 9)\*2.7777
Change From Baseline in Heart Failure Self-management Behaviors as Measured by the European Heart Failure Self-care Behavior Scale at 12 WeeksBaseline, 12 weeksThe instrument used will be 9-item European Heart Failure Self-care Behavior Scale (HSBS; standardized score from 0 to 100 (every item is given an equal weight) with a higher score meaning better self-care. Items are on a Likert scale of 1 - 5. For calculating the standardized score, each item is reverse coded and then computed using the formula: (Sum of all ever-coded items - 9)\*2.7777
Change From Baseline in Heart Failure Self-management Behaviors as Measured by the European Heart Failure Self-care Behavior Scale at 24 WeeksBaseline, 24 weeksThe instrument used will be 9-item European Heart Failure Self-care Behavior Scale (HSBS; standardized score from 0 to 100 (every item is given an equal weight) with a higher score meaning better self-care). Items are on a Likert scale of 1 - 5. For calculating the standardized score, each item is reverse coded and then computed using the formula: (Sum of all ever-coded items - 9)\*2.7777
Change From Baseline in Heart Failure-related Quality of Life (QOL) on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 6 WeeksBaseline, 6 weeksThe instrument used will be items 13 - 15 on the KCCQ. Values for the QoL domain range from 0 to 100 with higher scores indicating better quality of life. Domain score will be transformed to a 0 to 100 range by subtracting the lowest possible scale score, dividing by the range of the scale and multiplying by 100.
Change From Baseline in Heart Failure-related Quality of Life (QOL) on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 12 WeeksBaseline, 12 weeksThe instrument used will be items 13 - 15 on the KCCQ. Values for the QoL domain range from 0 to 100 with higher scores indicating better quality of life. Domain score will be transformed to a 0 to 100 range by subtracting the lowest possible scale score, dividing by the range of the scale and multiplying by 100.
Change From Baseline in Heart Failure-related Quality of Life (QOL) on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 24 WeeksBaseline, 24 weeksThe instrument used will be items 13 - 15 on the KCCQ. Values for the QoL domain range from 0 to 100 with higher scores indicating better quality of life. Domain score will be transformed to a 0 to 100 range by subtracting the lowest possible scale score, dividing by the range of the scale and multiplying by 100.
Change From Baseline in Heart Failure-related Functional Status on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 6 WeeksBaseline, 6 weeksThe instrument used will be items 1-12 on the KCCQ. Values for the functional status summary score from 0 to 100 with higher scores indicating better quality of life. Summary score will be transformed to a 0 to 100 range by subtracting the lowest possible scale score, dividing by the range of the scale and multiplying by 100.
Change From Baseline in Heart Failure-related Functional Status on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 12 WeeksBaseline, 12 weeksThe instrument used will be items 1-12 on the KCCQ. Values for the functional status summary score from 0 to 100 with higher scores indicating better quality of life. Summary score will be transformed to a 0 to 100 range by subtracting the lowest possible scale score, dividing by the range of the scale and multiplying by 100.
Change From Baseline in Heart Failure-related Functional Status on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 24 WeeksBaseline, 24 weeksThe instrument used will be items 1-12 on the KCCQ. Values for the functional status summary score from 0 to 100 with higher scores indicating better quality of life. Summary score will be transformed to a 0 to 100 range by subtracting the lowest possible scale score, dividing by the range of the scale and multiplying by 100.
Number of Heart Failure Hospitalizations in the Past 6 Months at End of 24 Weeks as Assessed by Self-reportBaseline, 24 weeksThis measure of number of cardiac hospitalizations in the past 6 months was obtained through participant self-report
Number of Days With Physical Activity on Sensor Logs at 6 Weeks6 weeksThis outcome measure will be measured by collecting number of days with physical activity data. These measures will be collected from sensor logs within the apps for both IG and CG.
Number of Heart Failure Hospitalizations in the Past Month at End of 6 Weeks as Assessed by Self-reportBaseline, 6 weeksThis measure will be obtained through participant self-report
Number of Heart Failure Hospitalizations in the Past Month at End of 24 Weeks as Assessed by Self-reportBaseline, 24 weeksThis measure will be obtained through participant self-report
Change From Baseline in Heart Failure Self-management Knowledge on Atlanta Heart Failure Knowledge Test (AHKT) at 6 WeeksBaseline, 6 weeksThe instrument used will be 30-item Atlanta Heart Failure Knowledge Test (AHFKT). Each correct answer is scored as 1 point, with no additional weighting of items; correct responses are then summed. Incorrect or skipped questions are awarded 0 points. Total scores range from 0 to 30. Higher scores indicate better HF knowledge
Change From Baseline in Heart Failure Self-management Knowledge on Atlanta Heart Failure Knowledge Test (AHKT) at 12 WeeksBaseline, 12 weeksThe instrument used will be 30-item Atlanta Heart Failure Knowledge Test (AHFKT). Each correct answer is scored as 1 point, with no additional weighting of items; correct responses are then summed. Incorrect or skipped questions are awarded 0 points. Total scores range from 0 to 30. Higher scores indicate better HF knowledge
Change From Baseline in Heart Failure Self-management Knowledge on Atlanta Heart Failure Knowledge Test (AHKT) at 24 WeeksBaseline,24 weeksThe instrument used will be 30-item Atlanta Heart Failure Knowledge Test (AHFKT). Each correct answer is scored as 1 point, with no additional weighting of items; correct responses are then summed. Incorrect or skipped questions are awarded 0 points. Total scores range from 0 to 30. Higher scores indicate better HF knowledge
Change From Baseline in Heart Failure Self-efficacy on Self-efficacy Section of Self-care of Heart Failure Index at 24 WeeksBaseline, 24 weeksThe instrument used will be 6-item Section C Self-efficacy section of Self-care of heart failure Index (SCHFI). Scores on the self-efficacy scale will range from 0 to 100, with higher scores reflecting better self-efficacy. To standardize scores the formula: (sum of Section C items - 6) \* 5.56 will be used.
Change From Baseline in Heart Failure Self-efficacy on Self-efficacy Section of Self-care of Heart Failure Index at 12 WeeksBaseline, 12 weeksThe instrument used will be 6-item Section C Self-efficacy section of Self-care of heart failure Index (SCHFI). Scores on the self-efficacy scale will range from 0 to 100, with higher scores reflecting better self-efficacy. To standardize scores the formula: (sum of Section C items - 6) \* 5.56 will be used.
Change From Baseline in Heart Failure Self-efficacy on Self-efficacy Section of Self-care of Heart Failure Index at 6 WeeksBaseline, 6 weeksThe instrument used will be 6-item Section C Self-efficacy section of Self-care of heart failure Index (SCHFI). Scores on the self-efficacy scale will range from 0 to 100, with higher scores reflecting better self-efficacy. To standardize scores the formula: (sum of Section C items - 6) \* 5.56 will be used.
Change From Baseline in Relative Autonomy Index (RAI) as Measured on Treatment Self-Regulation Questionnaire (TSRQ) at 6 WeeksBaseline, 6 weeksIn the 19-item Treatment Self-Regulation Questionnaire (TSRQ) adapted for heart failure, each item can receive a value ranging from 1 - 7, as selected by the participant. The scale has 2 sub-scales: autonomous and controlled motivation. Calculating the scores for the sub-scales will consist of averaging the items on that subscale. They are: Autonomous Regulation: 2, 3, 7, 10, 13, 16, 18, 19. Scores for Autonomous Regulation can range from 8 to 56. High scores indicate high autonomous motivation or intrinsic motivation for behavior engagement. Controlled Regulation: 1, 4, 5, 6, 8, 9, 11, 12, 14, 15, 17. Scores for Controlled Regulation can range from 8 to 56. High scores indicate high controlled motivation or extrinsic motivation for behavior engagement. Scoring for RAI will consist of subtracting the average for Controlled Regulation from the average for Autonomous Regulation. Higher RAI scores indicate higher autonomous or intrinsic motivation for behavior engagement.
Change From Baseline in Relative Autonomy Index (RAI) as Measured on Treatment Self-Regulation Questionnaire (TSRQ) at 12 WeeksBaseline, 12 weeksIn the 19-item Treatment Self-Regulation Questionnaire (TSRQ) adapted for heart failure, each item can receive a value ranging from 1 - 7, as selected by the participant. The scale has 2 sub-scales: autonomous and controlled motivation. Calculating the scores for the sub-scales will consist of averaging the items on that subscale. They are: Autonomous Regulation: 2, 3, 7, 10, 13, 16, 18, 19. Scores for Autonomous Regulation can range from 8 to 56. High scores indicate high autonomous motivation or intrinsic motivation for behavior engagement. Controlled Regulation: 1, 4, 5, 6, 8, 9, 11, 12, 14, 15, 17. Scores for Controlled Regulation can range from 8 to 56. High scores indicate high controlled motivation or extrinsic motivation for behavior engagement. Scoring for RAI will consist of subtracting the average for Controlled Regulation from the average for Autonomous Regulation. Higher RAI scores indicate higher autonomous or intrinsic motivation for behavior engagement.
Change From Baseline in Relative Autonomy Index (RAI) as Measured on Treatment Self-Regulation Questionnaire (TSRQ) at 24 WeeksBaseline, 24 weeksIn the 19-item Treatment Self-Regulation Questionnaire (TSRQ) adapted for heart failure, each item can receive a value ranging from 1 - 7, as selected by the participant. The scale has 2 sub-scales: autonomous and controlled motivation. Calculating the scores for the sub-scales will consist of averaging the items on that subscale. They are: Autonomous Regulation: 2, 3, 7, 10, 13, 16, 18, 19. Scores for Autonomous Regulation can range from 8 to 56. High scores indicate high autonomous motivation or intrinsic motivation for behavior engagement. Controlled Regulation: 1, 4, 5, 6, 8, 9, 11, 12, 14, 15, 17. Scores for Controlled Regulation can range from 8 to 56. High scores indicate high controlled motivation or extrinsic motivation for behavior engagement. Scoring for RAI will consist of subtracting the average for Controlled Regulation from the average for Autonomous Regulation. Higher RAI scores indicate higher autonomous or intrinsic motivation for behavior engagement.
Number of Heart Failure Hospitalizations in the Past Month at End of 12 Weeks as Assessed by Self-reportBaseline, 12 weeksThis measure will be obtained through participant self-report
Number of Days With Physical Activity on Sensor Logs at 12 Weeks12 weeksThis outcome measure will be measured by collecting number of days with physical activity data. These measures will be collected from sensor logs within the apps for both IG and CG.

Countries

United States

Participant flow

Participants by arm

ArmCount
Intervention Group
The intervention group will receive a sensor-controlled digital game (SCDG) app and weight monitoring and physical activity sensors Sensor-controlled digital game (SCDG): The SCDG will involve a narrative, the goal of which is to help an avatar in the game avoid rehospitalization by using game points, earned via the participant's real-time behaviors, in game tasks that help maintain the avatar's optimal HF health status. Real-time behaviors of weight-monitoring and physical activity will be tracked by an off-the-shelf sensors and app (Withings). The data from the Withings sensors will then be routed to our SCDG app. The digital game paired with sensors will enable objective tracking of real-time behaviors such as physical activity, and weight monitoring, and provide personalized, contextually relevant feedback (e.g., reduce fluid intake or call doctor for weight gain) to motivate engagement in and generate habit formation of heart failure related self-management behaviors.
19
Control Group
The control group will receive only the weight monitoring and physical activity sensors Sensor Only: Real-time behaviors of weight-monitoring and physical activity will be tracked by an off-the-shelf sensors and app (Withings). This group will also be provided with standardized evidence-based HF educational material.However, the data from the Withings sensors will not be routed to the SCDG.
19
Total38

Baseline characteristics

CharacteristicIntervention GroupControl GroupTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
8 Participants10 Participants18 Participants
Age, Categorical
Between 18 and 65 years
11 Participants9 Participants20 Participants
Duration with heart failure diagnosis
1 month to 1 year
8 Participants5 Participants13 Participants
Duration with heart failure diagnosis
> 1 year
6 Participants8 Participants14 Participants
Duration with heart failure diagnosis
< 30 days
5 Participants6 Participants11 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
3 Participants0 Participants3 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
16 Participants19 Participants35 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Last heart failure hospitalization
> 1 year
11 Participants11 Participants22 Participants
Last heart failure hospitalization
< 6 months
6 Participants5 Participants11 Participants
Last heart failure hospitalization
7 months to 1 year
2 Participants3 Participants5 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants1 Participants1 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
2 Participants4 Participants6 Participants
Race (NIH/OMB)
More than one race
1 Participants1 Participants2 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
16 Participants13 Participants29 Participants
Region of Enrollment
United States
19 participants19 participants38 participants
Sex: Female, Male
Female
10 Participants10 Participants20 Participants
Sex: Female, Male
Male
9 Participants9 Participants18 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 190 / 19
other
Total, other adverse events
0 / 190 / 19
serious
Total, serious adverse events
0 / 190 / 19

Outcome results

Primary

Number of Days With Weight-monitoring on Sensor Logs at 12 Weeks

This outcome will be measured by collecting number of days with weight-monitoring data. This measure will be collected from sensor logs within the apps for both intervention group (IG) and control group (CG).

Time frame: 12 weeks

Population: Based on participants available for data collection at 12 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupNumber of Days With Weight-monitoring on Sensor Logs at 12 Weeks69.7 daysStandard Deviation 16.1
Control GroupNumber of Days With Weight-monitoring on Sensor Logs at 12 Weeks60.1 daysStandard Deviation 18.7
Primary

Number of Days With Weight-monitoring on Sensor Logs at 6 Weeks

This outcome will be measured by collecting number of days with weight-monitoring data. This measure will be collected from sensor logs within the apps for both intervention group (IG) and control group (CG).

Time frame: 6 weeks

Population: Based on participants available for data collection at 6 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupNumber of Days With Weight-monitoring on Sensor Logs at 6 Weeks35.8 daysStandard Deviation 6
Control GroupNumber of Days With Weight-monitoring on Sensor Logs at 6 Weeks32.9 daysStandard Deviation 10.5
Secondary

Change From Baseline in Heart Failure-related Functional Status on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 12 Weeks

The instrument used will be items 1-12 on the KCCQ. Values for the functional status summary score from 0 to 100 with higher scores indicating better quality of life. Summary score will be transformed to a 0 to 100 range by subtracting the lowest possible scale score, dividing by the range of the scale and multiplying by 100.

Time frame: Baseline, 12 weeks

Population: Based on participants available for data collection for this measure at 12 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure-related Functional Status on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 12 Weeks3.7 score on a scaleStandard Deviation 14.1
Control GroupChange From Baseline in Heart Failure-related Functional Status on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 12 Weeks4.1 score on a scaleStandard Deviation 12.6
Secondary

Change From Baseline in Heart Failure-related Functional Status on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 24 Weeks

The instrument used will be items 1-12 on the KCCQ. Values for the functional status summary score from 0 to 100 with higher scores indicating better quality of life. Summary score will be transformed to a 0 to 100 range by subtracting the lowest possible scale score, dividing by the range of the scale and multiplying by 100.

Time frame: Baseline, 24 weeks

Population: Based on participants available for data collection for this measure at 24 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure-related Functional Status on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 24 Weeks7.4 score on a scaleStandard Deviation 10.7
Control GroupChange From Baseline in Heart Failure-related Functional Status on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 24 Weeks6.5 score on a scaleStandard Deviation 11.7
Secondary

Change From Baseline in Heart Failure-related Functional Status on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 6 Weeks

The instrument used will be items 1-12 on the KCCQ. Values for the functional status summary score from 0 to 100 with higher scores indicating better quality of life. Summary score will be transformed to a 0 to 100 range by subtracting the lowest possible scale score, dividing by the range of the scale and multiplying by 100.

Time frame: Baseline, 6 weeks

Population: Based on participants available for data collection for this measure at 6 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure-related Functional Status on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 6 Weeks6.9 score on a scaleStandard Deviation 14.1
Control GroupChange From Baseline in Heart Failure-related Functional Status on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 6 Weeks1.7 score on a scaleStandard Deviation 11.8
Secondary

Change From Baseline in Heart Failure-related Quality of Life (QOL) on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 12 Weeks

The instrument used will be items 13 - 15 on the KCCQ. Values for the QoL domain range from 0 to 100 with higher scores indicating better quality of life. Domain score will be transformed to a 0 to 100 range by subtracting the lowest possible scale score, dividing by the range of the scale and multiplying by 100.

Time frame: Baseline, 12 weeks

Population: Based on participants available for data collection for this measure at 12 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure-related Quality of Life (QOL) on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 12 Weeks8.2 score on a scaleStandard Deviation 13.5
Control GroupChange From Baseline in Heart Failure-related Quality of Life (QOL) on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 12 Weeks13.0 score on a scaleStandard Deviation 19.3
Secondary

Change From Baseline in Heart Failure-related Quality of Life (QOL) on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 24 Weeks

The instrument used will be items 13 - 15 on the KCCQ. Values for the QoL domain range from 0 to 100 with higher scores indicating better quality of life. Domain score will be transformed to a 0 to 100 range by subtracting the lowest possible scale score, dividing by the range of the scale and multiplying by 100.

Time frame: Baseline, 24 weeks

Population: Based on participants available for data collection for this measure at 24 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure-related Quality of Life (QOL) on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 24 Weeks10.8 score on a scaleStandard Deviation 16.9
Control GroupChange From Baseline in Heart Failure-related Quality of Life (QOL) on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 24 Weeks15.4 score on a scaleStandard Deviation 19.6
Secondary

Change From Baseline in Heart Failure-related Quality of Life (QOL) on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 6 Weeks

The instrument used will be items 13 - 15 on the KCCQ. Values for the QoL domain range from 0 to 100 with higher scores indicating better quality of life. Domain score will be transformed to a 0 to 100 range by subtracting the lowest possible scale score, dividing by the range of the scale and multiplying by 100.

Time frame: Baseline, 6 weeks

Population: Based on participants available for data collection for this measure at 6 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure-related Quality of Life (QOL) on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 6 Weeks5.8 score on a scaleStandard Deviation 13.1
Control GroupChange From Baseline in Heart Failure-related Quality of Life (QOL) on Kansas City Cardiomyopathy Questionnaire (KCCQ) at 6 Weeks8.7 score on a scaleStandard Deviation 15.3
Secondary

Change From Baseline in Heart Failure Self-efficacy on Self-efficacy Section of Self-care of Heart Failure Index at 12 Weeks

The instrument used will be 6-item Section C Self-efficacy section of Self-care of heart failure Index (SCHFI). Scores on the self-efficacy scale will range from 0 to 100, with higher scores reflecting better self-efficacy. To standardize scores the formula: (sum of Section C items - 6) \* 5.56 will be used.

Time frame: Baseline, 12 weeks

Population: Based on participants available for data collection for this measure at 12 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure Self-efficacy on Self-efficacy Section of Self-care of Heart Failure Index at 12 Weeks1.0 score on a scaleStandard Deviation 20.5
Control GroupChange From Baseline in Heart Failure Self-efficacy on Self-efficacy Section of Self-care of Heart Failure Index at 12 Weeks10.2 score on a scaleStandard Deviation 12.3
Secondary

Change From Baseline in Heart Failure Self-efficacy on Self-efficacy Section of Self-care of Heart Failure Index at 24 Weeks

The instrument used will be 6-item Section C Self-efficacy section of Self-care of heart failure Index (SCHFI). Scores on the self-efficacy scale will range from 0 to 100, with higher scores reflecting better self-efficacy. To standardize scores the formula: (sum of Section C items - 6) \* 5.56 will be used.

Time frame: Baseline, 24 weeks

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure Self-efficacy on Self-efficacy Section of Self-care of Heart Failure Index at 24 Weeks3.0 score on a scaleStandard Deviation 18
Control GroupChange From Baseline in Heart Failure Self-efficacy on Self-efficacy Section of Self-care of Heart Failure Index at 24 Weeks7.0 score on a scaleStandard Deviation 16.5
Secondary

Change From Baseline in Heart Failure Self-efficacy on Self-efficacy Section of Self-care of Heart Failure Index at 6 Weeks

The instrument used will be 6-item Section C Self-efficacy section of Self-care of heart failure Index (SCHFI). Scores on the self-efficacy scale will range from 0 to 100, with higher scores reflecting better self-efficacy. To standardize scores the formula: (sum of Section C items - 6) \* 5.56 will be used.

Time frame: Baseline, 6 weeks

Population: Based on participants available for data collection for this measure at 6 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure Self-efficacy on Self-efficacy Section of Self-care of Heart Failure Index at 6 Weeks2.2 score on a scaleStandard Deviation 25.7
Control GroupChange From Baseline in Heart Failure Self-efficacy on Self-efficacy Section of Self-care of Heart Failure Index at 6 Weeks6.9 score on a scaleStandard Deviation 18.1
Secondary

Change From Baseline in Heart Failure Self-management Behaviors as Measured by the European Heart Failure Self-care Behavior Scale at 12 Weeks

The instrument used will be 9-item European Heart Failure Self-care Behavior Scale (HSBS; standardized score from 0 to 100 (every item is given an equal weight) with a higher score meaning better self-care. Items are on a Likert scale of 1 - 5. For calculating the standardized score, each item is reverse coded and then computed using the formula: (Sum of all ever-coded items - 9)\*2.7777

Time frame: Baseline, 12 weeks

Population: Based on participants available for data collection for this measure at 12 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure Self-management Behaviors as Measured by the European Heart Failure Self-care Behavior Scale at 12 Weeks9.3 score on a scaleStandard Deviation 16.5
Control GroupChange From Baseline in Heart Failure Self-management Behaviors as Measured by the European Heart Failure Self-care Behavior Scale at 12 Weeks2.6 score on a scaleStandard Deviation 12.4
Secondary

Change From Baseline in Heart Failure Self-management Behaviors as Measured by the European Heart Failure Self-care Behavior Scale at 24 Weeks

The instrument used will be 9-item European Heart Failure Self-care Behavior Scale (HSBS; standardized score from 0 to 100 (every item is given an equal weight) with a higher score meaning better self-care). Items are on a Likert scale of 1 - 5. For calculating the standardized score, each item is reverse coded and then computed using the formula: (Sum of all ever-coded items - 9)\*2.7777

Time frame: Baseline, 24 weeks

Population: Based on participants available for data collection for this measure at 24 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure Self-management Behaviors as Measured by the European Heart Failure Self-care Behavior Scale at 24 Weeks10.2 score on a scaleStandard Deviation 13.4
Control GroupChange From Baseline in Heart Failure Self-management Behaviors as Measured by the European Heart Failure Self-care Behavior Scale at 24 Weeks0.5 score on a scaleStandard Deviation 9.8
Secondary

Change From Baseline in Heart Failure Self-management Behaviors as Measured by the European Heart Failure Self-care Behavior Scale at 6 Weeks

The instrument used will be 9-item European Heart Failure Self-care Behavior Scale (HSBS; standardized score from 0 to 100 (every item is given an equal weight) with a higher score meaning better self-care). Items are on a Likert scale of 1 - 5. For calculating the standardized score, each item is reverse coded and then computed using the formula: (Sum of all ever-coded items - 9)\*2.7777

Time frame: Baseline, 6 weeks

Population: Based on participants available for data collection for this measure at 6 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure Self-management Behaviors as Measured by the European Heart Failure Self-care Behavior Scale at 6 Weeks4.9 score on a scaleStandard Deviation 20.4
Control GroupChange From Baseline in Heart Failure Self-management Behaviors as Measured by the European Heart Failure Self-care Behavior Scale at 6 Weeks-2.7 score on a scaleStandard Deviation 9.9
Secondary

Change From Baseline in Heart Failure Self-management Knowledge on Atlanta Heart Failure Knowledge Test (AHKT) at 12 Weeks

The instrument used will be 30-item Atlanta Heart Failure Knowledge Test (AHFKT). Each correct answer is scored as 1 point, with no additional weighting of items; correct responses are then summed. Incorrect or skipped questions are awarded 0 points. Total scores range from 0 to 30. Higher scores indicate better HF knowledge

Time frame: Baseline, 12 weeks

Population: Based on participants available for data collection for this measure at 12 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure Self-management Knowledge on Atlanta Heart Failure Knowledge Test (AHKT) at 12 Weeks1.4 score on a scaleStandard Deviation 1.7
Control GroupChange From Baseline in Heart Failure Self-management Knowledge on Atlanta Heart Failure Knowledge Test (AHKT) at 12 Weeks1.1 score on a scaleStandard Deviation 1.5
Secondary

Change From Baseline in Heart Failure Self-management Knowledge on Atlanta Heart Failure Knowledge Test (AHKT) at 24 Weeks

The instrument used will be 30-item Atlanta Heart Failure Knowledge Test (AHFKT). Each correct answer is scored as 1 point, with no additional weighting of items; correct responses are then summed. Incorrect or skipped questions are awarded 0 points. Total scores range from 0 to 30. Higher scores indicate better HF knowledge

Time frame: Baseline,24 weeks

Population: Based on participants available for data collection for this measure at 24 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure Self-management Knowledge on Atlanta Heart Failure Knowledge Test (AHKT) at 24 Weeks1.1 score on a scaleStandard Deviation 2.1
Control GroupChange From Baseline in Heart Failure Self-management Knowledge on Atlanta Heart Failure Knowledge Test (AHKT) at 24 Weeks1.1 score on a scaleStandard Deviation 2.7
Secondary

Change From Baseline in Heart Failure Self-management Knowledge on Atlanta Heart Failure Knowledge Test (AHKT) at 6 Weeks

The instrument used will be 30-item Atlanta Heart Failure Knowledge Test (AHFKT). Each correct answer is scored as 1 point, with no additional weighting of items; correct responses are then summed. Incorrect or skipped questions are awarded 0 points. Total scores range from 0 to 30. Higher scores indicate better HF knowledge

Time frame: Baseline, 6 weeks

Population: Based on participants available for data collection for this measure at 6 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Heart Failure Self-management Knowledge on Atlanta Heart Failure Knowledge Test (AHKT) at 6 Weeks1.9 score on a scaleStandard Deviation 2.5
Control GroupChange From Baseline in Heart Failure Self-management Knowledge on Atlanta Heart Failure Knowledge Test (AHKT) at 6 Weeks2.1 score on a scaleStandard Deviation 2.5
Secondary

Change From Baseline in Relative Autonomy Index (RAI) as Measured on Treatment Self-Regulation Questionnaire (TSRQ) at 12 Weeks

In the 19-item Treatment Self-Regulation Questionnaire (TSRQ) adapted for heart failure, each item can receive a value ranging from 1 - 7, as selected by the participant. The scale has 2 sub-scales: autonomous and controlled motivation. Calculating the scores for the sub-scales will consist of averaging the items on that subscale. They are: Autonomous Regulation: 2, 3, 7, 10, 13, 16, 18, 19. Scores for Autonomous Regulation can range from 8 to 56. High scores indicate high autonomous motivation or intrinsic motivation for behavior engagement. Controlled Regulation: 1, 4, 5, 6, 8, 9, 11, 12, 14, 15, 17. Scores for Controlled Regulation can range from 8 to 56. High scores indicate high controlled motivation or extrinsic motivation for behavior engagement. Scoring for RAI will consist of subtracting the average for Controlled Regulation from the average for Autonomous Regulation. Higher RAI scores indicate higher autonomous or intrinsic motivation for behavior engagement.

Time frame: Baseline, 12 weeks

Population: Based on participants available for data collection for this measure at 12 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Relative Autonomy Index (RAI) as Measured on Treatment Self-Regulation Questionnaire (TSRQ) at 12 Weeks0.1 score on a scaleStandard Deviation 2.6
Control GroupChange From Baseline in Relative Autonomy Index (RAI) as Measured on Treatment Self-Regulation Questionnaire (TSRQ) at 12 Weeks-0.3 score on a scaleStandard Deviation 3
Secondary

Change From Baseline in Relative Autonomy Index (RAI) as Measured on Treatment Self-Regulation Questionnaire (TSRQ) at 24 Weeks

In the 19-item Treatment Self-Regulation Questionnaire (TSRQ) adapted for heart failure, each item can receive a value ranging from 1 - 7, as selected by the participant. The scale has 2 sub-scales: autonomous and controlled motivation. Calculating the scores for the sub-scales will consist of averaging the items on that subscale. They are: Autonomous Regulation: 2, 3, 7, 10, 13, 16, 18, 19. Scores for Autonomous Regulation can range from 8 to 56. High scores indicate high autonomous motivation or intrinsic motivation for behavior engagement. Controlled Regulation: 1, 4, 5, 6, 8, 9, 11, 12, 14, 15, 17. Scores for Controlled Regulation can range from 8 to 56. High scores indicate high controlled motivation or extrinsic motivation for behavior engagement. Scoring for RAI will consist of subtracting the average for Controlled Regulation from the average for Autonomous Regulation. Higher RAI scores indicate higher autonomous or intrinsic motivation for behavior engagement.

Time frame: Baseline, 24 weeks

Population: Based on participants available for data collection for this measure at 24 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Relative Autonomy Index (RAI) as Measured on Treatment Self-Regulation Questionnaire (TSRQ) at 24 Weeks-0.6 score on a scaleStandard Deviation 2.5
Control GroupChange From Baseline in Relative Autonomy Index (RAI) as Measured on Treatment Self-Regulation Questionnaire (TSRQ) at 24 Weeks-0.2 score on a scaleStandard Deviation 2.7
Secondary

Change From Baseline in Relative Autonomy Index (RAI) as Measured on Treatment Self-Regulation Questionnaire (TSRQ) at 6 Weeks

In the 19-item Treatment Self-Regulation Questionnaire (TSRQ) adapted for heart failure, each item can receive a value ranging from 1 - 7, as selected by the participant. The scale has 2 sub-scales: autonomous and controlled motivation. Calculating the scores for the sub-scales will consist of averaging the items on that subscale. They are: Autonomous Regulation: 2, 3, 7, 10, 13, 16, 18, 19. Scores for Autonomous Regulation can range from 8 to 56. High scores indicate high autonomous motivation or intrinsic motivation for behavior engagement. Controlled Regulation: 1, 4, 5, 6, 8, 9, 11, 12, 14, 15, 17. Scores for Controlled Regulation can range from 8 to 56. High scores indicate high controlled motivation or extrinsic motivation for behavior engagement. Scoring for RAI will consist of subtracting the average for Controlled Regulation from the average for Autonomous Regulation. Higher RAI scores indicate higher autonomous or intrinsic motivation for behavior engagement.

Time frame: Baseline, 6 weeks

Population: Based on participants available for data collection for this measure at 6 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupChange From Baseline in Relative Autonomy Index (RAI) as Measured on Treatment Self-Regulation Questionnaire (TSRQ) at 6 Weeks-0.1 score on a scaleStandard Deviation 1.2
Control GroupChange From Baseline in Relative Autonomy Index (RAI) as Measured on Treatment Self-Regulation Questionnaire (TSRQ) at 6 Weeks-0.2 score on a scaleStandard Deviation 2.2
Secondary

Mean of Daily Steps on Physical Activity Sensor Logs at 12 Weeks

This outcome measure will be measured by calculating the average daily steps at end of 12 weeks. These measures will be collected from sensor logs within the apps for both IG and CG.

Time frame: 12 weeks

Population: Based on participants available for data collection at 12 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupMean of Daily Steps on Physical Activity Sensor Logs at 12 Weeks2887 stepsStandard Deviation 2821
Control GroupMean of Daily Steps on Physical Activity Sensor Logs at 12 Weeks2541 stepsStandard Deviation 1604
Secondary

Mean of Daily Steps on Physical Activity Sensor Logs at 6 Weeks

This outcome measure will be measured by calculating the average daily steps at end of 6 weeks. These measures will be collected from sensor logs within the apps for both IG and CG.

Time frame: 6 weeks

Population: Based on participants available for data collection at 6 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupMean of Daily Steps on Physical Activity Sensor Logs at 6 Weeks2742 stepsStandard Deviation 2499
Control GroupMean of Daily Steps on Physical Activity Sensor Logs at 6 Weeks2638 stepsStandard Deviation 1573
Secondary

Number of Days With Physical Activity on Sensor Logs at 12 Weeks

This outcome measure will be measured by collecting number of days with physical activity data. These measures will be collected from sensor logs within the apps for both IG and CG.

Time frame: 12 weeks

Population: Based on participants available for data collection at 12 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupNumber of Days With Physical Activity on Sensor Logs at 12 Weeks76.6 daysStandard Deviation 11.02
Control GroupNumber of Days With Physical Activity on Sensor Logs at 12 Weeks69.6 daysStandard Deviation 17.3
Secondary

Number of Days With Physical Activity on Sensor Logs at 6 Weeks

This outcome measure will be measured by collecting number of days with physical activity data. These measures will be collected from sensor logs within the apps for both IG and CG.

Time frame: 6 weeks

Population: Based on participants available for data collection at 6 weeks.

ArmMeasureValue (MEAN)Dispersion
Intervention GroupNumber of Days With Physical Activity on Sensor Logs at 6 Weeks36.7 DaysStandard Deviation 10.9
Control GroupNumber of Days With Physical Activity on Sensor Logs at 6 Weeks39.2 DaysStandard Deviation 6.6
Secondary

Number of Heart Failure Hospitalizations in the Past 6 Months at End of 24 Weeks as Assessed by Self-report

This measure of number of cardiac hospitalizations in the past 6 months was obtained through participant self-report

Time frame: Baseline, 24 weeks

Population: Based on participants available for data collection for this measure at 24 weeks.

ArmMeasureValue (NUMBER)
Intervention GroupNumber of Heart Failure Hospitalizations in the Past 6 Months at End of 24 Weeks as Assessed by Self-report2 hospitalizations
Control GroupNumber of Heart Failure Hospitalizations in the Past 6 Months at End of 24 Weeks as Assessed by Self-report2 hospitalizations
Secondary

Number of Heart Failure Hospitalizations in the Past Month at End of 12 Weeks as Assessed by Self-report

This measure will be obtained through participant self-report

Time frame: Baseline, 12 weeks

Population: Based on participants available for data collection for this measure at 12 weeks.

ArmMeasureValue (NUMBER)
Intervention GroupNumber of Heart Failure Hospitalizations in the Past Month at End of 12 Weeks as Assessed by Self-report0 hospitalizations
Control GroupNumber of Heart Failure Hospitalizations in the Past Month at End of 12 Weeks as Assessed by Self-report1 hospitalizations
Secondary

Number of Heart Failure Hospitalizations in the Past Month at End of 24 Weeks as Assessed by Self-report

This measure will be obtained through participant self-report

Time frame: Baseline, 24 weeks

Population: Based on participants available for data collection for this measure at 24 weeks.

ArmMeasureValue (NUMBER)
Intervention GroupNumber of Heart Failure Hospitalizations in the Past Month at End of 24 Weeks as Assessed by Self-report1 hospitalizations
Control GroupNumber of Heart Failure Hospitalizations in the Past Month at End of 24 Weeks as Assessed by Self-report0 hospitalizations
Secondary

Number of Heart Failure Hospitalizations in the Past Month at End of 6 Weeks as Assessed by Self-report

This measure will be obtained through participant self-report

Time frame: Baseline, 6 weeks

Population: Based on participants available for data collection for this measure at 6 weeks.

ArmMeasureValue (NUMBER)
Intervention GroupNumber of Heart Failure Hospitalizations in the Past Month at End of 6 Weeks as Assessed by Self-report1 hospitalizations
Control GroupNumber of Heart Failure Hospitalizations in the Past Month at End of 6 Weeks as Assessed by Self-report1 hospitalizations

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026