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Clinical Trials/NCT02004158
NCT02004158
Completed
Not Applicable

Study of a Positive Psychology Program to Improve Healthy Behaviors After an Acute Coronary Syndrome: Proof of Concept Study

Massachusetts General Hospital1 site in 1 country23 target enrollmentNovember 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Coronary Syndrome
Sponsor
Massachusetts General Hospital
Enrollment
23
Locations
1
Primary Endpoint
Rate of Exercise Completion
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

In this proof-of-concept study, the investigators will assess the ease and usefulness of a positive psychology program in patients with acute coronary syndrome and less-than-optimal adherence to health behaviors. The investigators believe that positive psychology (a field that studies boosting positive emotions rather than simply reducing negative emotions) will help this cardiac population to be more healthy. The investigators want to determine whether this positive psychology program has the potential to be an adjunctive treatment for cardiac populations.

Registry
clinicaltrials.gov
Start Date
November 2013
End Date
September 2014
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jeff C. Huffman, MD

Director, Cardiac Psychiatry Research Program

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Adult patients admitted to one of three cardiac inpatient units at Massachusetts General Hospital.
  • Primary diagnosis of acute coronary syndrome (myocardial infarction or unstable angina).
  • Less-than-optimal adherence to health behaviors. This will be defined as a mean score of less than 15 on the Medical Outcomes Study Specific Adherence Scale (scores range from 3-18, with higher scores indicating better adherence).

Exclusion Criteria

  • Cognitive deficits, assessed via a 6-item cognitive screen used to assess appropriate participation of medically-ill patients in research studies.
  • Patients not prescribed aspirin at discharge.
  • Inability to communicate in English.
  • Inability to participate in physical activity.

Outcomes

Primary Outcomes

Rate of Exercise Completion

Time Frame: 8 weeks

Rate of exercise completion will be measured by the number of participants who have a good rate of completion of exercises. There are 8 exercises in total. A good rate of completion will be defined as an average of 5 or more exercises completed per subject.

Ease of Exercises

Time Frame: 8 weeks

Ease of exercises will be measured by a self-report 10-point Likert scale (0=not easy to complete, 10=very easy to complete). Ease will be defined as an average score of 6 or more on this scale.

Self-reported Psychological Impact of Exercises

Time Frame: 8 weeks

Psychological impact of exercises will be measured by two self-reported 10-point Likert scales. One scale measures optimism after completing the exercise (0=not optimistic, 10=very optimistic), and the other scale measures happiness after completing the exercise (0=not happy, 10=very happy). Psychological impact will be defined as an average score of 6 or more on both of these scales.

Secondary Outcomes

  • Objective Psychological Impact of Exercises(8 weeks)

Study Sites (1)

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