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Internet-delivered Cognitive Behavior Therapy Compared to Stress Management for Atrial Fibrillation

Primary Purpose

Atrial Fibrillation, Arrythmia

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Internet-deliviered exposure-based CBT
Internet-delivered stress management treatment
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Paroxysmal AF ≥ once per month that causes moderate to severe symptoms and leads to significant distress or interferes with daily life (i.e. EHRA class ≥ IIb);
  • Scoring ≥ 20 on the Cardiac Anxiety Questionnaire at screening;
  • Age 18-75 years;
  • 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 ablation for AF or ablation within 3 months before assessment;
  • Other severe medical illness;
  • Any medical restriction to physical exercise;
  • Severe psychiatric disorder, severe depression, or risk of suicide;
  • Alcohol dependency;
  • Previous participation in any AF-CBT study conducted by the research group.

Sites / Locations

  • Karolinska universitetssjukhuset Solna

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Internet-delivered exposure-focused CBT

Internet-delivered stress management treatment

Arm Description

Internet-delivered CBT over 10 weeks The CBT treatment lasts for 10 weeks and includes the following: Education on the role of anxiety on cardiac function and the effects of symptom preoccupation and avoidance QoL and depression in AF, creating a vicious cycle; exposure to physical sensations that are similar to AF symptoms (e.g.,palpitations due to physical activity or stress) to reduce fear of these symptoms; exposure to situations or activities previously avoided and abolishment of behaviors that aim to control symptoms; and behavioral activation aiming to increase social and physical activity and reduce depressive symptoms. Therapist support is provided at least once weekly through the platform developed for the purpose. Therapists are trained CBT-psychologists.

Stress management treatment for 10 weeks Participants randomized to The Stress Management Treatment will receive 10 weeks of stress managemen including relaxation technics, standard life style advice regarding physical activity, sleep and and standardized AF-information in line with current guidelines for AF. Therapist support is provided at least once weekly through the platform developed for the purpose. Therapists are trained CBT-psychologists.

Outcomes

Primary Outcome Measures

Atrial Fibrillation Effect on Quality-of-Life modified for weekly assessment
The AFEQT is an atrial fibrillation-specific measure that taps into the QoL-domains: symptoms, daily activities, treatment concern, and treatment satisfaction. Total score ranges from 0 (severe symptoms and disability) to 100 (no symptoms and disability).
Atrial Fibrillation Effect on Quality-of-Life modified for weekly assessment
The AFEQT is an atrial fibrillation-specific measure that taps into the QoL-domains: symptoms, daily activities, treatment concern, and treatment satisfaction. Total score ranges from 0 (severe symptoms and disability) to 100 (no symptoms and disability).

Secondary Outcome Measures

Cardiac Anxiety Questionnaire (CAQ)
Measure of cardiac anxiety, fear, avoidance and attention. The score ranges between 0 and 72, with a greater score indicating elevated cardiac anxiety.
Cardiac Anxiety Questionnaire (CAQ)
Measure of cardiac anxiety, fear, avoidance and attention. The score ranges between 0 and 72, with a greater score indicating elevated cardiac anxiety.
AF-avoidance behavior questionnaire
Form measuring AF-specific avoidance- and control behaviors, developed by the research group
AF-avoidance behavior questionnaire
Form measuring AF-specific avoidance- and control behaviors, developed by the research group
AF-avoidance behavior questionnaire modified for weekly assessment
4 items from the AF-avoidance behavior questionnaire
Short Form Health Survey (SF-12)
General quality of life, with a score ranging from 0 to 100. A higher score indicating a better quality of life
Short Form Health Survey (SF-12)
General quality of life, with a score ranging from 0 to 100. A higher score indicating a better quality of life
Atrial Fibrillation Severity Scale (4 items)
4 items from the Atrial Fibrillation Severity Scale, measuring health care seeking
Atrial Fibrillation Severity Scale (4 items)
4 items from the Atrial Fibrillation Severity Scale, measuring health care seeking
The Godin-Shepard Leisure-Time Physical Activity Questionnaire
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.
The Godin-Shepard Leisure-Time Physical Activity Questionnaire
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.
Body Sensation Questionnaire
Fear of bodily symptoms, score ranging from 0 to 72 . Higher scores indicate more fear of body sensations.
Body Sensation Questionnaire
Fear of bodily symptoms, score ranging from 0 to 72 . Higher scores indicate more fear of body sensations.
Patient Health Questionnaire-2
Short form measuring depression, score ranging 0 to 6 with a higher score indicating higher level of depression.
Patient Health Questionnaire-2
Short form measuring depression, score ranging 0 to 6 ,with a higher score indicating higher level of depression.
Perceived Stress Scale (4 items version)
Measures perceived stress, score ranging from 0-16, with a higher score indicating higher level of perceived stress
Perceived Stress Scale (4 items version)
Measures perceived stress, score ranging from 0-16, with a higher score indicating higher level of perceived stress
Generalized Anxiety Disorder-2 (GAD-2)
General anxiety, score ranging from 0-6, with a higher score indicating more anxiety and worry.
Generalized Anxiety Disorder-2
General anxiety, score ranging from 0-6, with a higher score indicating more anxiety and worry.
Insomnia Severity Index (5 items)
Measure of insomnia, score ranging from 0-20, with a higher score indicating more severe insomnia
Insomnia Severity Index (5 items)
Measure of insomnia, score ranging from 0-20, with a higher score indicating more severe insomnia
Perceived Competence Scale
Perception of AF-specific knowledge and competence, score ranging from 0- 50 with higher score indicating higher perceived competence
Perceived Competence Scale
Perception of AF-specific knowledge and competence, score ranging from 0- 50 with higher score indicating higher perceived competence
Client Satisfaction Questionnaire
Treatment satisfaction, score ranging from 0-24, with a higher score indicating higher satisfaction with treatment.
Adverse events
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').
Adverse events
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').
Symptoms Checklist Severity and Frequency Scale (SCL)
AF-related symptoms
Symptoms Checklist Severity and Frequency Scale (SCL)
AF-related symptoms measured in two sub scales A) frequency: score ranging from 0-48, with higher score indicating higher frequency of symptoms, B) severity of experienced symptom: score ranging from 0- 48, with a higher score indicating more severe symptoms
AFFS/SCL-4
4 items derived from the Symptoms Checklist (SCL) and the Atrial Fibrillation Severity Scale (AFSS) measuring disabling cardiac symptoms not specified in AFEQT
AFFS/SCL-4
4 items derived from the Symptoms Checklist (SCL) and the Atrial Fibrillation Severity Scale (AFSS) measuring disabling cardiac symptoms not specified in AFEQT

Full Information

First Posted
June 24, 2021
Last Updated
October 10, 2023
Sponsor
Karolinska Institutet
Collaborators
Karolinska University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04962932
Brief Title
Internet-delivered Cognitive Behavior Therapy Compared to Stress Management for Atrial Fibrillation
Official Title
Internet-delivered Cognitive Behavior Therapy Compared to Stress Management for Atrial Fibrillation- a Randomized Controlled Trial With Active Control
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
August 13, 2021 (Actual)
Primary Completion Date
March 31, 2023 (Actual)
Study Completion Date
October 5, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Karolinska University Hospital

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 aim of this study is to evaluate if internet- delivered cognitive behavior therapy (CBT), based on exposure principles and behavioral activation, improves QoL and symptom burden in patients with symptomatic atrial fibrillation (AF), controlling for expectancy of improvement and attention from a caregiver, using an active control group (stress management). The study will include 260 patients with symptomatic AF despite optimal medical treatment in accordance with current guidelines.
Detailed Description
Atrial fibrillation (AF) is the most common cardiac arrhythmia (irregular heartbeat) affecting 3% of the population. AF is associated with poor quality of life (QoL) and large costs for society. In a considerable proportion of patients, AF symptoms (e.g., palpitations, fatigue, and chest pain) are not alleviated by current medical or interventional treatments. Psychological factors can worsen AF symptoms, and anxiety and depression are common among AF patients. Symptom preoccupation and avoidance of social and physical activities are likely to play important roles in the development of anxiety, depression, disability and healthcare utilization. The aim is to evaluate if CBT, based on behavioral activation and exposure principles, improves wellbeing and QoL in symptomatic AF patients controlling for expectancy of improvement and attention from a caregiver using an active control group receiving stress management treatment (SMT). Method: A randomized controlled trial. Participants are randomized to internet- delivered exposure-based CBT (N=130) or to SMT (N=130). Participants in both groups receive weekly therapist support through online written communication. The internet-delivered SMT-treatment includes life-style advice (e.g., exercise, sleep advice), relaxation and problem-solving skills to reduce stress. Both treatments lasts 10 weeks and are comparable regarding number of treatment modules, treatment burden and attention from the treating psychologist.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation, Arrythmia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
206 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Internet-delivered exposure-focused CBT
Arm Type
Experimental
Arm Description
Internet-delivered CBT over 10 weeks The CBT treatment lasts for 10 weeks and includes the following: Education on the role of anxiety on cardiac function and the effects of symptom preoccupation and avoidance QoL and depression in AF, creating a vicious cycle; exposure to physical sensations that are similar to AF symptoms (e.g.,palpitations due to physical activity or stress) to reduce fear of these symptoms; exposure to situations or activities previously avoided and abolishment of behaviors that aim to control symptoms; and behavioral activation aiming to increase social and physical activity and reduce depressive symptoms. Therapist support is provided at least once weekly through the platform developed for the purpose. Therapists are trained CBT-psychologists.
Arm Title
Internet-delivered stress management treatment
Arm Type
Active Comparator
Arm Description
Stress management treatment for 10 weeks Participants randomized to The Stress Management Treatment will receive 10 weeks of stress managemen including relaxation technics, standard life style advice regarding physical activity, sleep and and standardized AF-information in line with current guidelines for AF. Therapist support is provided at least once weekly through the platform developed for the purpose. Therapists are trained CBT-psychologists.
Intervention Type
Behavioral
Intervention Name(s)
Internet-deliviered exposure-based CBT
Intervention Description
The intervention lasts for 10 weeks and include: Education, Interoceptive exposure, exposure in-vivo, combining in-vivo exposure with interoceptive exposure, behavioral activation and relapse prevention. Include the guidance of a minimum weekly contact with a CBT psychologist.
Intervention Type
Behavioral
Intervention Name(s)
Internet-delivered stress management treatment
Intervention Description
The intervention last for 10 weeks and include: Internet-SMT include life-style advice (e.g., exercise, sleep advice), relaxation and problem-solving skills to reduce stress. Patients are offered regular online contact with a psychologist with the same frequency and intensity as in the CBT arm.
Primary Outcome Measure Information:
Title
Atrial Fibrillation Effect on Quality-of-Life modified for weekly assessment
Description
The AFEQT is an atrial fibrillation-specific measure that taps into the QoL-domains: symptoms, daily activities, treatment concern, and treatment satisfaction. Total score ranges from 0 (severe symptoms and disability) to 100 (no symptoms and disability).
Time Frame
Change over 11 measurement points measured from baseline and weekly for 10 weeks during treatment [PRIMARY ENDPOINT]
Title
Atrial Fibrillation Effect on Quality-of-Life modified for weekly assessment
Description
The AFEQT is an atrial fibrillation-specific measure that taps into the QoL-domains: symptoms, daily activities, treatment concern, and treatment satisfaction. Total score ranges from 0 (severe symptoms and disability) to 100 (no symptoms and disability).
Time Frame
From baseline to 9 months
Secondary Outcome Measure Information:
Title
Cardiac Anxiety Questionnaire (CAQ)
Description
Measure of cardiac anxiety, fear, avoidance and attention. The score ranges between 0 and 72, with a greater score indicating elevated cardiac anxiety.
Time Frame
From baseline to 10 weeks
Title
Cardiac Anxiety Questionnaire (CAQ)
Description
Measure of cardiac anxiety, fear, avoidance and attention. The score ranges between 0 and 72, with a greater score indicating elevated cardiac anxiety.
Time Frame
From baseline to 9 months
Title
AF-avoidance behavior questionnaire
Description
Form measuring AF-specific avoidance- and control behaviors, developed by the research group
Time Frame
From baseline to 10 weeks
Title
AF-avoidance behavior questionnaire
Description
Form measuring AF-specific avoidance- and control behaviors, developed by the research group
Time Frame
From baseline to 9 months
Title
AF-avoidance behavior questionnaire modified for weekly assessment
Description
4 items from the AF-avoidance behavior questionnaire
Time Frame
Change over 11 measurement points measured from baseline and weekly for 10 weeks during treatment
Title
Short Form Health Survey (SF-12)
Description
General quality of life, with a score ranging from 0 to 100. A higher score indicating a better quality of life
Time Frame
From baseline to 10 weeks
Title
Short Form Health Survey (SF-12)
Description
General quality of life, with a score ranging from 0 to 100. A higher score indicating a better quality of life
Time Frame
From baseline to 9 months
Title
Atrial Fibrillation Severity Scale (4 items)
Description
4 items from the Atrial Fibrillation Severity Scale, measuring health care seeking
Time Frame
From baseline to 10 weeks
Title
Atrial Fibrillation Severity Scale (4 items)
Description
4 items from the Atrial Fibrillation Severity Scale, measuring health care seeking
Time Frame
From baseline to 9 months
Title
The Godin-Shepard Leisure-Time Physical Activity Questionnaire
Description
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.
Time Frame
From baseline to 10 weeks
Title
The Godin-Shepard Leisure-Time Physical Activity Questionnaire
Description
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.
Time Frame
From baseline to 9 months
Title
Body Sensation Questionnaire
Description
Fear of bodily symptoms, score ranging from 0 to 72 . Higher scores indicate more fear of body sensations.
Time Frame
From baseline to 10 weeks
Title
Body Sensation Questionnaire
Description
Fear of bodily symptoms, score ranging from 0 to 72 . Higher scores indicate more fear of body sensations.
Time Frame
From baseline to 9 months
Title
Patient Health Questionnaire-2
Description
Short form measuring depression, score ranging 0 to 6 with a higher score indicating higher level of depression.
Time Frame
From baseline to 10 weeks
Title
Patient Health Questionnaire-2
Description
Short form measuring depression, score ranging 0 to 6 ,with a higher score indicating higher level of depression.
Time Frame
From baseline to 9 months
Title
Perceived Stress Scale (4 items version)
Description
Measures perceived stress, score ranging from 0-16, with a higher score indicating higher level of perceived stress
Time Frame
From baseline to 10 weeks
Title
Perceived Stress Scale (4 items version)
Description
Measures perceived stress, score ranging from 0-16, with a higher score indicating higher level of perceived stress
Time Frame
From baseline to 9 months
Title
Generalized Anxiety Disorder-2 (GAD-2)
Description
General anxiety, score ranging from 0-6, with a higher score indicating more anxiety and worry.
Time Frame
From baseline to 10 weeks
Title
Generalized Anxiety Disorder-2
Description
General anxiety, score ranging from 0-6, with a higher score indicating more anxiety and worry.
Time Frame
From baseline to 9 months
Title
Insomnia Severity Index (5 items)
Description
Measure of insomnia, score ranging from 0-20, with a higher score indicating more severe insomnia
Time Frame
From baseline to 10 weeks
Title
Insomnia Severity Index (5 items)
Description
Measure of insomnia, score ranging from 0-20, with a higher score indicating more severe insomnia
Time Frame
From Baseline to 9 months
Title
Perceived Competence Scale
Description
Perception of AF-specific knowledge and competence, score ranging from 0- 50 with higher score indicating higher perceived competence
Time Frame
From baseline to 10 weeks
Title
Perceived Competence Scale
Description
Perception of AF-specific knowledge and competence, score ranging from 0- 50 with higher score indicating higher perceived competence
Time Frame
From baseline to 9 months
Title
Client Satisfaction Questionnaire
Description
Treatment satisfaction, score ranging from 0-24, with a higher score indicating higher satisfaction with treatment.
Time Frame
10 weeks from baseline
Title
Adverse events
Description
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').
Time Frame
10 weeks from baseline
Title
Adverse events
Description
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').
Time Frame
9 months from baseline
Title
Symptoms Checklist Severity and Frequency Scale (SCL)
Description
AF-related symptoms
Time Frame
From baseline to 10 weeks
Title
Symptoms Checklist Severity and Frequency Scale (SCL)
Description
AF-related symptoms measured in two sub scales A) frequency: score ranging from 0-48, with higher score indicating higher frequency of symptoms, B) severity of experienced symptom: score ranging from 0- 48, with a higher score indicating more severe symptoms
Time Frame
From baseline to 9 months
Title
AFFS/SCL-4
Description
4 items derived from the Symptoms Checklist (SCL) and the Atrial Fibrillation Severity Scale (AFSS) measuring disabling cardiac symptoms not specified in AFEQT
Time Frame
Weekly from baseline to 10 weeks
Title
AFFS/SCL-4
Description
4 items derived from the Symptoms Checklist (SCL) and the Atrial Fibrillation Severity Scale (AFSS) measuring disabling cardiac symptoms not specified in AFEQT
Time Frame
From baseline to 9 months
Other Pre-specified Outcome Measures:
Title
Psychosocial stressors and changes in physical health
Description
Participants are asked about their self-perceived health and if they have experienced any stressful event that they believe have affected their health (e.g severe disease, death of close relative, divorce)
Time Frame
10 weeks from baseline
Title
Psychosocial stressors and changes in physical health
Description
Participants are asked about their self-perceived health and if they have experienced any stressful event that they believe have affected their health (e.g severe disease, death of close relative, divorce)
Time Frame
9 months from baseline
Title
Background data
Description
Demographics, list of medications, co-morbidity, smoking history and alcohol consumption
Time Frame
Baseline
Title
Treatment Credibility Scale
Description
Measures treatment credibility
Time Frame
2-4 weeks from baseline
Title
Working Alliance Inventory
Description
Measures therapeutic alliance with the psychologist
Time Frame
2-4 weeks from baseline
Title
Changes in medication
Description
Participants are asked if they have made any changes in medication
Time Frame
10 weeks from baseline
Title
Changes in medication
Description
Participants are asked if they have made any changes in medication
Time Frame
9 months from baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Paroxysmal AF ≥ once per month that causes moderate to severe symptoms and leads to significant distress or interferes with daily life (i.e. EHRA class ≥ IIb); Scoring ≥ 20 on the Cardiac Anxiety Questionnaire at screening; Age 18-75 years; 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 ablation for AF or ablation within 3 months before assessment; Other severe medical illness; Any medical restriction to physical exercise; Severe psychiatric disorder, severe depression, or risk of suicide; Alcohol dependency; Previous participation in any AF-CBT study conducted by the research group.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brjann Ljotsson, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska universitetssjukhuset Solna
City
Solna
ZIP/Postal Code
171 64
Country
Sweden

12. IPD Sharing Statement

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Internet-delivered Cognitive Behavior Therapy Compared to Stress Management for Atrial Fibrillation

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