ACS - Acute Coronary Syndrome
Conditions
Keywords
ACS, Positive Psychology, Motivational Interviewing, Positive emotions
Brief summary
This study is a single-arm, 12-week trial to test the feasibility of a PP-MI intervention for patients recently admitted following ACS. PP-MI is a novel positive psychology-based health behavior intervention that is adapted for patients hospitalized for ACS. The intervention aims to cultivate positive emotions in this vulnerable population that could provide broad and significant health benefits, and may have distinct-and more powerful-effects than simply attempting to dampen negative emotions. The primary aim is to assess whether the intervention exercises are feasible and linked with immediate boosts in positive affect upon completion. The secondary goal is to provide the research team with greater experience recruiting inpatients with an ACS, successfully completing intervention sessions, and administering psychological and medical assessments by phone.
Detailed description
The initial study visit will occur in-person two weeks after discharge from the hospital. Participants will meet with a member of the study staff (the study trainer) and complete self-report questionnaires assessing health behavior adherence and mental and physical health. Then, a study interventionist will provide a treatment manual for the positive psychology + motivational interviewing intervention, review the rationale for the initial exercise, and assign the first exercise. If the participant is in the positive psychology + motivational interviewing condition, the trainer will explain the rationale for both the positive psychology and goal-setting and motivational interviewing portions of the program, and will be assigned the first exercise. Participants will then be given an accelerometer, which they will be asked to wear for 7 days to ensure that they are comfortable with the device and that useable data can be obtained from the participant. Participants will then complete twelve 30-minute weekly phone sessions with a study trainer. The phone sessions primarily will include a review of the prior week's session content and a discussion of the rationale and assignment of the next week's exercise/assignment. Upon the completion of these calls, a blinded member of the study staff will call participants to administer self-report outcome measures. Participants will also be asked to wear an accelerometer at the follow-up timepoint as an objective measure of physical activity, which they will return by mail to the study staff.
Interventions
For the positive psychology portion of the intervention, the study trainer will (a) review the week's positive psychology exercise, (b) discuss the rationale of the next week's positive psychology exercise through a guided review of the positive psychology manual, and (c) assign the next week's positive psychology exercise. For the motivational interviewing portion, participants will (a) review their physical activity goal from the prior week, (b) discuss techniques for improving physical activity, and (c) set a physical activity goal for the next week. Study trainers will use motivational interviewing techniques to facilitate goal setting.
Sponsors
Northwestern University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Eligible patients must meet at least two of three World Health Organization criteria for an acute MI: typical chest pain, elevated cardiac enzymes, and electrocardiographic changes consistent with MI. For UA, participants must have new-onset angina within 2 months, exacerbation of previous angina with rest or with minimal exercise, or angina within 2 weeks of MI. * Suboptimal adherence to health behaviors: eligible patients must meet a total item score of \<15 (suboptimal) based on three Medical Outcomes Study-Specific Adherence Scale (MOS SAS) items OR a total item score of 15 and a physical activity item score of \<5.
Exclusion criteria
* Cognitive deficits, assessed via a 6-item cognitive screen,33 used to assess appropriate participation of medically ill patients in research studies and defined by a score of \< 4. * Medical conditions precluding interviews or likely to lead to death within 6 months, determined in consultation with the primary treatment team and Dr. James Flaherty. * Individuals who have undergone coronary artery bypass surgery, or any open heart surgery, in the past 1 year. * Inability to perform moderate to vigorous physical activity, as defined by an inability to walk without aid of an assistive device such as a walker or cane, OR inability to walk at a steady pace for at least 5 minutes without stopping. * Inability to communicate in English.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of intervention sessions completed by participants | 12 weeks | Measured by number of intervention sessions completed by participants |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in medication adherence | Baseline, 12 week | Measured by SRMA, a two-item self-report medication adherence scale measuring percentage of time patients report taking their heart medications in the past one and two weeks. |
| Change in dietary adherence | Baseline, 12 week | Measured by the MEDFICTS scale, a National Cholesterol Education Program-developed scale inquiring about saturated fat. |
| Change in positive affect | Baseline, 12 week | Measured by the Positive and Negative Affect Schedule (PANAS) |
| Change in trait optimism | Baseline, 12 week | Measured by the Life Orientation Test-Revised (LOT-R) |
| Change in state optimism | Baseline, 12 week | Measured by the State Optimism Scale developed by Dr. Jeff Huffman |
| Change in anxiety | Baseline, 12 week | Measured by the anxiety subscale of the Hospital Anxiety and Depression Scale (HADS-A) |
| Change in physical activity | Baseline, 12 week | As measured by accelerometer |
| Change in physical function | Baseline, 12 week | Measured by the Duke Activity Status Index (DASI) |
| Change in health-related quality of life | Baseline, 12 week | Measured by the Short Form 12 (SF-12) |
| Change in adherence to health behaviors | Baseline, 12 week | Measured by the three items from the Medical Outcomes Study-Specific Adherence Scale (MOS SAS) |
| Change in cardiac symptoms | Baseline, 12 week | Measured by a checklist taken from the Women and Ischemia Syndrome Evaluation Study |
| Change in perceived stress | Baseline, 12 week | Measured by the perceived stress scale (PSS-4) measure |
| Change in depression | Baseline, 12 week | Measured by the depression subscale of the Hospital Anxiety and Depression Scale (HADS-D) |
Countries
United States
Outcome results
None listed