The purpose of this study is to evaluate early preliminary efficacy of the eMotion intervention in US adults who have experienced a first cardiac event and participating in phase II cardiac rehabilitation. This study will evaluate early efficacy and evaluate the cognitive processes as intervention response variables. Investigators will also examine the relationships between emotion regulation and other cognitive processes and symptoms (threat and stress, cognition and motivation), symptoms \[depression, anxiety, pain, sleep, and fatigue\]), and health related quality of life among adults enrolled in cardiac rehabilitation after a first cardiac event.
Aim 1: Evaluate early preliminary efficacy of the eMotion intervention Research hypothesis 1. Compared with adults randomized to active healthy living attention control and usual care control groups, adults randomized to eMotion will have greater improvement in these outcomes over time: 1.1. Improved minutes of moderate to vigorous physical activity 1.2. Symptom improvement (depression, anxiety, pain, sleep, and fatigue) 1.3. Health related quality of life. Aim 2: Evaluate the cognitive processes as intervention response variables. Research hypothesis 2. Compared with adults randomized to active healthy living attention control and usual care control groups, adults randomized to eMotion will have: 2.1. Improved emotion regulation (efficiency and strategy use) 2.2. Decreased perceived cardiac threat and general stress 2.3. Improved cognition and motivation Aim 3. Exploratory. Examine the relationships between emotion regulation and other cognitive processes and symptoms (threat and stress, cognition and motivation), and symptoms \[depression, anxiety, pain, sleep, and fatigue\]) among adults enrolled in cardiac rehabilitation after a first major cardiac event.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
TRIPLE
Enrollment
40
Content is delivered within the context of emotion provoking situations common in those recovering from a first MI and in maintaining MVPA. The new on-demand access to asynchronous content sessions provides didactic presentation of video and written material based on weekly needs assessments. Weekly scheduled synchronous video chat sessions, led by a nurse interventionist, will provide further individualization and application of content materials.
The attention control group will receive their usual cardiac rehabilitation and a comparable dose matched (to that of the eMotion intervention) of healthy living web content and video chat with a nurse.
Indiana University Health West Hospital
Avon, Indiana, United States
Indiana University Health Bedford Hospital
Bedford, Indiana, United States
Indiana University Health Methodist Hospital
Indianapolis, Indiana, United States
Indiana University Health Tipton Hospital
Tipton, Indiana, United States
Change in Moderate to Vigorous Physical Activity (MVPA)
Minutes spent in MVPA
Time frame: 1 week trials at baseline, 12 weeks, 20 weeks, and 52 weeks
Change in Depression Symptoms
Symptoms of depression measured using the Depression, Anxiety, and Stress Scale (DASS)
Time frame: Baseline to 12 weeks, 20 weeks, and 52 weeks
Change in Anxiety Symptoms
Symptoms of anxiety measured using the Depression, Anxiety, and Stress Scale (DASS)
Time frame: Baseline to 12 weeks, 20 weeks, and 52 weeks
Change in Pain Symptoms
Pain will be measured with the Brief Pain Inventory
Time frame: Baseline to 12 weeks, 20 weeks, and 52 weeks
Change in Sleep efficiency
Sleep efficiency will be a calculation of the ratio of the total sleep time to time spent in bed using the ActiGraph wGT3X-BT accelerometer
Time frame: Baseline to 12 weeks, 20 weeks, and 52 weeks
Change in Fatigue Symptoms
Fatigue will be measured using the Fatigue Severity Scale
Time frame: Baseline to 12 weeks, 20 weeks, and 52 weeks
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