MI-CBT: Internet-delivered Cognitive Behavioral Therapy Following Myocardial Infarction

Sponsor
Karolinska Institutet (Other)
Overall Status
Recruiting
CT.gov ID
NCT05128981
Collaborator
(none)
30
1
1
13
2.3

Study Details

Study Description

Brief Summary

Myocardial infarction (MI) is one of the leading cause s of health loss globally, representing a large proportion of general disability. Anxiety and depression occur in 20-30 percent of patients following MI and have been identified as risk factors for recurrent adverse cardiac event. The purpose of our this study is to develop and evaluate a disease specific cognitive behavioral therapy (C BT) protocol to reduce cardia anxiety, depression, increase physical inactivity and quality of life (Q oL) in patients following MI

Condition or Disease Intervention/Treatment Phase
  • Behavioral: MI-CBT
N/A

Detailed Description

The study will include 30 patients. The MI-specific CBT lasts for 8 weeks and is therapist guided and delivered via internet via a secure digital platform by licensed psychologists expertise in CBT for cardiac disease or final year psychologist under supervision. During treatment, the psychologists will have direct access to a cardiologist assigned to the project and treatments are conducted in close interdisciplinary collaboration to ensure patient safety

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Internet-delivered Cognitive Behavioral Therapy Following Myocardial Infarction
Actual Study Start Date :
Oct 28, 2021
Anticipated Primary Completion Date :
Nov 28, 2022
Anticipated Study Completion Date :
Nov 28, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: MI-CBT via the Internet

The MI-specific CBT will consist of 8 modules delivered via the Internet with home assignments that can be reviewed and reported in the research groups secure platform.

Behavioral: MI-CBT
Education of MI and common reactions, Interoceptive exposure, Exposure in-vivo, Behavioral activation, Relapse prevention

Outcome Measures

Primary Outcome Measures

  1. 12-Item Short-Form Health Survey (SF-12) [Baseline]

    General quality of life, with a score ranging from 0 to 100. A higher score indicating a better quality of life. General quality of life, with a score ranging from 0 to 100. A higher score indicating a better quality of life. General quality of life, with a score ranging from 0 to 100. A higher score indicating a better quality of life.

  2. 12-Item Short-Form Health Survey (SF-12) [2 months from baseline]

    General quality of life, with a score ranging from 0 to 100. A higher score indicating a better quality of life. General quality of life, with a score ranging from 0 to 100. A higher score indicating a better quality of life. General quality of life, with a score ranging from 0 to 100. A higher score indicating a better quality of life.

  3. 12-Item Short-Form Health Survey (SF-12) [8 months from baseline]

    General quality of life, with a score ranging from 0 to 100. A higher score indicating a better quality of life. General quality of life, with a score ranging from 0 to 100. A higher score indicating a better quality of life. General quality of life, with a score ranging from 0 to 100. A higher score indicating a better quality of life.

Secondary Outcome Measures

  1. Cardiac anxiety questionnaire [Baseline]

    Measure of cardiac anxiety, fear, avoidance and attention. The score ranges between 0 and 72, with a greater score indicating elevated cardiac anxiety.

  2. Cardiac anxiety questionnaire [2 months from baseline]

    Measure of cardiac anxiety, fear, avoidance and attention. The score ranges between 0 and 72, with a greater score indicating elevated cardiac anxiety.

  3. Cardiac anxiety questionnaire [8 months from baseline]

    Measure of cardiac anxiety, fear, avoidance and attention. The score ranges between 0 and 72, with a greater score indicating elevated cardiac anxiety.

  4. Body Sensation Questionnaire [Baseline]

    Fear of bodily symptoms, score ranging from 0 to 72 . Higher scores indicate more fear of body sensations. Fear of bodily symptoms, score ranging from 0 to 72 . Higher scores indicate more fear of body sensations. Fear of bodily symptoms, score ranging from 0 to 72 . Higher scores indicate more fear of body sensations.

  5. Body Sensation Questionnaire [2 months from baseline]

    Fear of bodily symptoms, score ranging from 0 to 72 . Higher scores indicate more fear of body sensations. Fear of bodily symptoms, score ranging from 0 to 72 . Higher scores indicate more fear of body sensations. Fear of bodily symptoms, score ranging from 0 to 72 . Higher scores indicate more fear of body sensations.

  6. Body Sensation Questionnaire [8 months from baseline]

    Fear of bodily symptoms, score ranging from 0 to 72 . Higher scores indicate more fear of body sensations. Fear of bodily symptoms, score ranging from 0 to 72 . Higher scores indicate more fear of body sensations. Fear of bodily symptoms, score ranging from 0 to 72 . Higher scores indicate more fear of body sensations.

  7. Patient Health Questionnaire-9 [Baseline]

    Measure of depression, score ranging 0 to 27 with a higher score indicating higher level of depression

  8. Patient Health Questionnaire-9 [2 months from baseline]

    Measure of depression, score ranging 0 to 27 with a higher score indicating higher level of depression

  9. Patient Health Questionnaire-9 [8 months from baseline]

    Measure of depression, score ranging 0 to 27 with a higher score indicating higher level of depression

  10. Generalized Anxiety Disorder 7-item [Baseline]

    General anxiety, score ranging from 0-21, with a higher score indicating more anxiety and worry.

  11. Generalized Anxiety Disorder 7-item [2 months from baseline]

    General anxiety, score ranging from 0-21, with a higher score indicating more anxiety and worry.

  12. Generalized Anxiety Disorder 7-item [8 months from baseline]

    General anxiety, score ranging from 0-21, with a higher score indicating more anxiety and worry.

  13. The Godin Leisure-time Exercise [Baseline]

    Level of physical activity. The participant rate numbers of time per week that they engage in physical activity. The numb ers are the categorized in to low, moderate, and high levels of physical activity.

  14. The Godin Leisure-time Exercise [2 months from baseline]

    Level of physical activity. The participant rate numbers of time per week that they engage in physical activity. The numb ers are the categorized in to low, moderate, and high levels of physical activity.

  15. The Godin Leisure-time Exercise [8 months from baseline]

    Level of physical activity. The participant rate numbers of time per week that they engage in physical activity. The numb ers are the categorized in to low, moderate, and high levels of physical activity.

  16. Tampas Scale for Kinesophobia-Heart version [Baseline]

    Fear of physical activity. The total score varies between 17 and 68, with higher values indicating more severe kinesiophobia.

  17. Tampas Scale for Kinesophobia-Heart version [2 months from baseline]

    Fear of physical activity. The total score varies between 17 and 68, with higher values indicating more severe kinesiophobia.

  18. Tampas Scale for Kinesophobia-Heart version [8 months from baseline]

    Fear of physical activity. The total score varies between 17 and 68, with higher values indicating more severe kinesiophobia.

  19. Client satisfaction Questionnaire [Baseline]

    Treatment satisfaction, score ranging from 0 to 32, with a higher score indication more satisfaction with the treatment.

  20. Client satisfaction Questionnaire [2 months from baseline]

    Treatment satisfaction, score ranging from 0 to 32, with a higher score indication more satisfaction with the treatment.

  21. Adverse events [2 months from treatment]

    Potential adverse reactions to the treatment. Participants will be asked to report and rate the short- and long term discomfort of the adverse event on a scale from 0 ('did not affect me at all') and 3 ('affected me very negatively').

  22. Adverse events [8 months from treatment]

    Potential adverse reactions to the treatment. Participants will be asked to report and rate the short- and long term discomfort of the adverse event on a scale from 0 ('did not affect me at all') and 3 ('affected me very negatively').

  23. Symptom Checklist (SCL) [Baseline]

    Measures frequency and severity of 16 cardiac-related symptoms. Scoring range from 0 to 64 for frequency with a greater score indicating more frequent symptoms, and from range from 0 to 48 for severity, with a greater score indicating more severe symptoms

  24. Symptom Checklist (SCL) [2 months from baseline]

    Measures frequency and severity of 16 cardiac-related symptoms. Scoring range from 0 to 64 for frequency with a greater score indicating more frequent symptoms, and from range from 0 to 48 for severity, with a greater score indicating more severe symptoms

  25. Symptom Checklist (SCL) [8 months from baseline]

    Measures frequency and severity of 16 cardiac-related symptoms. Scoring range from 0 to 64 for frequency with a greater score indicating more frequent symptoms, and from range from 0 to 48 for severity, with a greater score indicating more severe symptoms

  26. Perceived stress scale (4-item version) [Baseline]

    Stress reactivity. A greater score indicate more perceived stress.

  27. Perceived stress scale (4-item version) [2 months from Baseline]

    Stress reactivity. A greater score indicate more perceived stress.

  28. Perceived stress scale (4-item version) [8 months from Baseline]

    Stress reactivity. A greater score indicate more perceived stress.

  29. Insomnia Severity Index [Baseline]

    Measurement of sleep

  30. Insomnia Severity Index [2 months from Baseline]

    Measure of insomnia, score ranging from 0-20, with a higher score indicating more severe insomnia

  31. Insomnia Severity Index [8 months from Baseline]

    Measure of insomnia, score ranging from 0-20, with a higher score indicating more severe insomnia

  32. The Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5) [Baseline]

    Measure of post traumatic stress, score ranging from 0-80, with a higher score indicating more post traumatic stress.

  33. The Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5) [2 months from Baseline]

    Measure of post traumatic stress, score ranging from 0-80, with a higher score indicating more post traumatic stress.

  34. The Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5) [8 months from Baseline]

    Measure of post traumatic stress, score ranging from 0-80, with a higher score indicating more post traumatic stress.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

( - )MI ≥ 6 months before assessment ( - )Age 18-75 years endorsed cardiac anxiety that leads to significant distress or interferes with daily life (Cardiac Anxiety Questionnaire (CAQ); score ≥20) ( - ) On optimal medical treatment ( - )Able to read and write in Swedish.

Exclusion Criteria:

( - ) heart failure with severe systolic dysfunction (ejection fraction ≤ 35%) ( - ) significant valvular disease ( - ) planned coronary artery bypass surgery or other invasive therapy ( - ) other severe medical illness ( - )any medical restriction to physical exercise ( - )severe psychiatric disorder, severe depression, or risk of suicide ( - )alcohol dependency

Contacts and Locations

Locations

Site City State Country Postal Code
1 Karolinska Institutet Stockholm Sweden

Sponsors and Collaborators

  • Karolinska Institutet

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Josefin Särnholm, PhD, Karolinska Institutet
ClinicalTrials.gov Identifier:
NCT05128981
Other Study ID Numbers:
  • CBT-MI
First Posted:
Nov 22, 2021
Last Update Posted:
Nov 22, 2021
Last Verified:
Nov 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 22, 2021