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Effects of Exergaming to Reduce Sedentary Time in Inactive Patients With Heart Failure (Heart-eXg)

Primary Purpose

Cardiovascular Diseases

Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Heart Farming
Sponsored by
Linkoeping University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cardiovascular Diseases

Eligibility Criteria

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

Inclusion Criteria: Diagnosed with symptomatic HF (NYHA II-IV) as diagnosed by cardiologist, (independent of Ejection Fraction: Patients with a preserved ejection fraction (HFpEF), mid-range ejection fraction (HFmrREF) or reduced ejection fraction (HFrEF) can be included. Clinically stable Physically inactive by self-report * (see 6.3.1) Older than 18 years, there is no upper age limit, Speak/understand the language of the country where the study is taking place. Wanting to use a smartphone for the study (if patients do not have a smartphone, they can borrow it from the study team for the duration of the study) Exclusion Criteria: Unable to use an exergame due to visual, hearing, cognitive impairment assessed by HF nurse or cardiologist. Not being able to perform the 6-minute walk test. Not being able or willing to wear an activity monitor. Currently included in a rehabilitation program Lack of willingness to play an exergame. Co-morbidity that hinders benefitting for this form of exercise (history of stroke, severe cognitive dysfunction, or a life expectancy shorter than 6 months).

Sites / Locations

  • Kalmar LänssjukhusetRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Exergame group

Control group

Arm Description

Patients will be introduced to the exergame and the exergame will be installed following a protocol either by the patients themselves or an instructor of the study. Patients will be advised to exergame daily based on their activity monitor reading at baseline and based on their current activity level and preferences. During the 3 months of active intervention patients will receive feedback on their activity level and data will also be shared with the coach who will use it to adapt the gaming advice. A clear exergaming goal will be set together by patient and coach. In the first month, they will receive weekly feedback on their performance based on the readings from the activity monitor and the reading from the exergame. In the rest of the active study team the frequency of the contact with the coach will be personalized.

Patients will receive a protocol-based activity advice (one time) from the HF team (nurse, cardiologist and/or physiotherapist) that corresponds to the intervention group in terms of time and effort. Participants in the control group are encouraged to decrease their sedentary behaviour to the same extent as the intervention group, and if possible be physical active 30 minutes for 5 days a week.

Outcomes

Primary Outcome Measures

Sedentary time
Sedentary time measured with activity monitor Actigraph

Secondary Outcome Measures

Exercise Capacity
6-minute walk test
Frailty
Fried Frailty tests
Clinical frailty
Clinical Frailty Scale: a frailty score ranging from 1 (very fit) to 9 (terminally ill)
Heart Failure specific Quality of Life
12 item Kansas City Cardiomyopathy inlcudes that quantifies physical limitations, symptom frequency, Quality of Life, and social limitation, along with a summary scores for each domain, scoring from 0 to 100. Zero denoting the worst and 100 the best possible health status.
General Quality of Life
EuroQol-5 Dimension 5 levels (EQ-5D) includes five domain scales (mobility, self-care, usual activities, pain and discomfort, and anxiety and depression) and five levels for each domain. A higher score in the EQ-5D-5L indicated better HRQOL
Sedentary time
Sedentary time measured with activity monitor Actigraph

Full Information

First Posted
May 17, 2022
Last Updated
December 6, 2022
Sponsor
Linkoeping University
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1. Study Identification

Unique Protocol Identification Number
NCT05641662
Brief Title
Effects of Exergaming to Reduce Sedentary Time in Inactive Patients With Heart Failure
Acronym
Heart-eXg
Official Title
Heart-eXg Study: Effects of Exergaming to Reduce Sedentary Time in Inactive Patients With Heart Failure: An International Multi-center, Randomized, Parallel-group Study
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 16, 2022 (Actual)
Primary Completion Date
August 16, 2023 (Anticipated)
Study Completion Date
April 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
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
The goal of this to determine the effect of tailored exergaming for inactive patients with heart failure to reduce their sedentary time, improve their daily physical activity, exercise capacity, decrease frailty and improve health-related quality of life. Participants will, on a background of standard guideline-directed medical therapy patients, be randomised to tailored activity advice (control) or the Heart-Exergame (Heart-eXg) intervention for a period of 3 months. Patients randomised to the Heart-eXg group will receive an exergame with feedback and tailoring to adapt the exergaming advice. Patients will also be able to play with a person in their own network.
Detailed Description
Rationale: Heart failure (HF) is an increasing global health concern with over 20 million patients worldwide. A decrease in sedentary time can have beneficial effects for a growing group of inactive patients with HF. The use of exergames (games to improve physical activity) is promising for people who are home bound and physically inactive. Such a gaming activity should be attractive, tailored to preferences and to capacity. Objective: To determine the effect of tailored exergaming for inactive patients with HF to reduce their sedentary time, improve their daily physical activity, exercise capacity, decrease frailty and improve health-related quality of life. Study design: A pilot study and a multicentre, open-label 1:1 randomised clinical trial with 6 months follow-up. Study population: Adult patients with symptomatic HF: n= 20 for the pilot study and n=600 for the main study Intervention: On a background of standard guideline-directed medical therapy patients will be randomised to tailored activity advice (control) or the Heart-Exergame (Heart-eXg) intervention for a period of 3 months. Patients randomised to the Heart-eXg group will receive an exergame with feedback and tailoring to adapt the exergaming advice. Patients will also be able to play with a person in their own network. Main study parameters/endpoints: Primary endpoint is sedentary time (actigraphy). Secondary outcomes are daily physical activity, submaximal exercise capacity, physical frailty, health-related quality of life. This study will gain insight into the effects of using an exergame that is easily applicable and affordable. Given the vast growing target population of patients with HF worldwide, and the simplicity of the intervention, potentially millions of patients may benefit from the results of this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Diseases

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigator
Allocation
Randomized
Enrollment
750 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Exergame group
Arm Type
Experimental
Arm Description
Patients will be introduced to the exergame and the exergame will be installed following a protocol either by the patients themselves or an instructor of the study. Patients will be advised to exergame daily based on their activity monitor reading at baseline and based on their current activity level and preferences. During the 3 months of active intervention patients will receive feedback on their activity level and data will also be shared with the coach who will use it to adapt the gaming advice. A clear exergaming goal will be set together by patient and coach. In the first month, they will receive weekly feedback on their performance based on the readings from the activity monitor and the reading from the exergame. In the rest of the active study team the frequency of the contact with the coach will be personalized.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Patients will receive a protocol-based activity advice (one time) from the HF team (nurse, cardiologist and/or physiotherapist) that corresponds to the intervention group in terms of time and effort. Participants in the control group are encouraged to decrease their sedentary behaviour to the same extent as the intervention group, and if possible be physical active 30 minutes for 5 days a week.
Intervention Type
Other
Intervention Name(s)
Heart Farming
Intervention Description
Heart Farming is a mobile game. which can be played indoors and outdoors and stimulates players to be physically active. The game is built around a theme (farming) and users are challenged to collect products by being active. The phone will register movements and convert them into points and fruits and vegetables. For the basic playing only 10 minutes walking a day with the game is possible and is rewarded. For players who want more challenge and level of trading products and collecting products in groups is added. The game is adaptable to different levels of mobility and players can invite others to play with them. Players can see their own game results, progression, and active time.
Primary Outcome Measure Information:
Title
Sedentary time
Description
Sedentary time measured with activity monitor Actigraph
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Exercise Capacity
Description
6-minute walk test
Time Frame
Baseline, 3 months and 6 months
Title
Frailty
Description
Fried Frailty tests
Time Frame
Baseline, 3 months and 6 months
Title
Clinical frailty
Description
Clinical Frailty Scale: a frailty score ranging from 1 (very fit) to 9 (terminally ill)
Time Frame
Baseline, 3 months and 6 months
Title
Heart Failure specific Quality of Life
Description
12 item Kansas City Cardiomyopathy inlcudes that quantifies physical limitations, symptom frequency, Quality of Life, and social limitation, along with a summary scores for each domain, scoring from 0 to 100. Zero denoting the worst and 100 the best possible health status.
Time Frame
Baseline, 3 months and 6 months
Title
General Quality of Life
Description
EuroQol-5 Dimension 5 levels (EQ-5D) includes five domain scales (mobility, self-care, usual activities, pain and discomfort, and anxiety and depression) and five levels for each domain. A higher score in the EQ-5D-5L indicated better HRQOL
Time Frame
Baseline, 3 months and 6 months
Title
Sedentary time
Description
Sedentary time measured with activity monitor Actigraph
Time Frame
6 months
Other Pre-specified Outcome Measures:
Title
Patient expectations
Description
Open ended interview questions
Time Frame
Baseline and 6 months
Title
Exercise motivation
Description
The situational motivation scale (SIMS): 16 items measuring four forms of motivation with exh four items (amotivation, external, identified, and intrinsic motivation). Each item is rated on a 7-point Likert scale ranging from 1 "corresponds not at all" to 7 "corresponds exactly." The score of each form of motivation ranges from 4-28, with a higher score meaning higher motivation.
Time Frame
Baseline, 3 months and 6 months
Title
Cost
Description
Cost logbook
Time Frame
6 months
Title
Willingness to pay
Description
Interviews
Time Frame
6 months
Title
Time exergaming
Description
Record time exergaming
Time Frame
During the 6 months intervention
Title
Enjoyment physical activity
Description
Exergaming Enjoyment Scale, 20 items, scoring ranging from 20-100
Time Frame
3 and 6 months in the intervention group only
Title
Cognitive function
Description
Montreal Cognitive Assessment (MoCA)
Time Frame
Baseline, 3 months and 6 months
Title
Social and daily function
Description
Canadian Occupational Performance Measure (COPM)
Time Frame
Baseline, 3 months and 6 months
Title
Depression
Description
Hospital Anxiety and Depression scale( HADs): two conjoint 7-item subscales, one specifically targeted at anxiety (HADS-A) and one focussing on depression (HADS-D). Raw scores of between 8 and 10 identify mild cases of depression or anxiety, 11-15 moderate cases, and 16 or above, severe cases.
Time Frame
Baseline, 3 months and 6 months
Title
Self-care
Description
European Self-Care Behavioural Scale (ESCBS): nine statements about HF-specific self-care which have to be rated on a 5-point Likert scale ('completely agree' and 'I don't agree at all').The sum score of range from 9 to 45, with lower scores indicating better self-care.
Time Frame
Baseline, 3 months and 6 months
Title
Knowledge
Description
Heart Failure Knowledge Scale: 15-item, self-administered questionnaire that covers items concerning HF knowledge in general, knowledge on HF treatment (including diet and fluid restriction) and HF symptoms and symptom recognition. The scale has a minimum score of 0 (no knowledge) and a maximum score of 15 points (optimal knowledge).
Time Frame
Baseline
Title
Clinical Data
Description
Clinical data from patient journal
Time Frame
Baseline
Title
Adverse events
Description
Number of adverse events
Time Frame
Throughout the trial of 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed with symptomatic HF (NYHA II-IV) as diagnosed by cardiologist, (independent of Ejection Fraction: Patients with a preserved ejection fraction (HFpEF), mid-range ejection fraction (HFmrREF) or reduced ejection fraction (HFrEF) can be included. Clinically stable Physically inactive by self-report * (see 6.3.1) Older than 18 years, there is no upper age limit, Speak/understand the language of the country where the study is taking place. Wanting to use a smartphone for the study (if patients do not have a smartphone, they can borrow it from the study team for the duration of the study) Exclusion Criteria: Unable to use an exergame due to visual, hearing, cognitive impairment assessed by HF nurse or cardiologist. Not being able to perform the 6-minute walk test. Not being able or willing to wear an activity monitor. Currently included in a rehabilitation program Lack of willingness to play an exergame. Co-morbidity that hinders benefitting for this form of exercise (history of stroke, severe cognitive dysfunction, or a life expectancy shorter than 6 months).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tiny Jaarsma, PhD
Phone
+46011363550
Email
tiny.jaarsma@liu.se
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
Kalmar Länssjukhuset
City
Kalmar
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tiny Jaarsma

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
http://www.heart-exg.com/index.php
Description
Study website

Learn more about this trial

Effects of Exergaming to Reduce Sedentary Time in Inactive Patients With Heart Failure

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