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Internet-delivered Cognitive Behavior Therapy for Atrial Fibrillation

Primary Purpose

Atrial Fibrillation, Arrhythmia

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Internet-delivered cognitive behavior therapy
Treatment as usual
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:

  • Inclusion criteria: A) 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) ; B) Age 18-75 years; C) On optimal medical treatment; D). Able to read and write in Swedish.

Exclusion Criteria:

  • (E) heart failure with severe systolic dysfunction (ejection fraction ≤ 35%); (F) significant valvular disease; (G) planned ablation for AF or ablation within 3 months before assessment; (H) other severe medical illness; (I) any medical restriction to physical exercise; (J) severe psychiatric disorder, severe depression, or risk of suicide; (K) alcohol dependency.

Sites / Locations

  • Karolinska universitetssjukhuset Solna

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Internet-delivered CBT over 10 weeks

Treatment as usual wait list

Arm Description

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.

Patients randomized to the treatment as usual wait list arm will receive standardized AF information that emphasizes that an active physical and social lifestyle is necessary to maintain good health. Thus, the treatment as usual arm will control for the provision of basic patient information, but without the guidance of a psychologist or any CBT interventions.

Outcomes

Primary Outcome Measures

The Atrial Fibrillation Quality of Life (AFEQT)
The AFEQT is an atrial fibrillation-specific measure that taps into the QoL-domains: symptoms, daily activities, treatment concern, and treatment satisfaction.
The Atrial Fibrillation Quality of Life (AFEQT)
The AFEQT is an atrial fibrillation-specific measure that taps into the QoL-domains: symptoms, daily activities, treatment concern, and treatment satisfaction.
The Atrial Fibrillation Quality of Life (AFEQT)
The AFEQT is an atrial fibrillation-specific measure that taps into the QoL-domains: symptoms, daily activities, treatment concern, and treatment satisfaction.
The Atrial Fibrillation Quality of Life (AFEQT)
The AFEQT is an atrial fibrillation-specific measure that taps into the QoL-domains: symptoms, daily activities, treatment concern, and treatment satisfaction.

Secondary Outcome Measures

Electrocardiography (ECG) measurement
Change in symptomatic burden. The patient will undergo 5 days ECG assessment in order to measure objectively symptomatic burden (number and duration of symptomatic AF episodes and symptomatic "non-AF episodes")
ECG measurement
Change in symptomatic burden. The patient will undergo 5 days ECG assessment in order to measure objectively symptomatic burden (number and duration of symptomatic AF episodes and symptomatic "non-AF episodes")
ECG measurement
Change in symptomatic burden. The patient will undergo 5 days ECG assessment in order to measure objectively symptomatic burden (number and duration of symptomatic AF episodes and symptomatic "non-AF episodes")
Cardiac Anxiety Questionary (CAQ)
Symptom preoccupation
Cardiac Anxiety Questionary (CAQ)
Symptom preoccupation
Cardiac Anxiety Questionary (CAQ)
Symptom preoccupation
Cardiac Anxiety Questionary (CAQ)
Symptom preoccupation
the World Health Organization Disability Assessment Schedule (WHODAS 2.0, 12- item version)
General quality of life
WHODAS 2.0 (12-item version)
General quality of life
WHODAS 2.0 (12-item version)
General quality of life
Symptom checklist Severity and Frequency Scale (SCL)
AF related symptoms
Symptom checklist Severity and Frequency Scale (SCL)
AF related symptoms
Symptom checklist Severity and Frequency Scale (SCL)
AF related symptoms
Atrial Fibrillation Severity Scale
Symptomatic burden
Atrial Fibrillation Severity Scale
Symptomatic burden
Atrial Fibrillation Severity Scale
Symptomatic burden
Patient Health Questionnaire (PHQ-9)
Depression
PHQ-9
Depression
PHQ-9
Depression
Client satisfaction Questionnaire
Treatment satisfaction
Adverse events
Potential adverse reactions to the treatment

Full Information

First Posted
December 11, 2017
Last Updated
September 21, 2020
Sponsor
Karolinska Institutet
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1. Study Identification

Unique Protocol Identification Number
NCT03378349
Brief Title
Internet-delivered Cognitive Behavior Therapy for Atrial Fibrillation
Official Title
Internet-delivered Cognitive Behavior Therapy for Atrial Fibrillation - a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
January 8, 2018 (Actual)
Primary Completion Date
December 20, 2019 (Actual)
Study Completion Date
September 20, 2020 (Actual)

3. Sponsor/Collaborators

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

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 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) compared to treatment as usual. The study will include 120 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 more than a wait list offered treatment as usual. Method: A randomized controlled trial. Participants are randomized to internet-delivered CBT for 10 weeks (N=60) or to treatment as usual (N=60). The internet-delivered CBT-program will last for 10 weeks and include weekly therapist support, consisting of online messages and telephone calls. Patients on the treatment as usual wait list will be provided standardized written information about basic self-management in AF. The treatment as usual wait list will be crossed over to treatment 3 months after the treatment group has completed treatment.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
126 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Internet-delivered CBT over 10 weeks
Arm Type
Experimental
Arm Description
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
Treatment as usual wait list
Arm Type
Placebo Comparator
Arm Description
Patients randomized to the treatment as usual wait list arm will receive standardized AF information that emphasizes that an active physical and social lifestyle is necessary to maintain good health. Thus, the treatment as usual arm will control for the provision of basic patient information, but without the guidance of a psychologist or any CBT interventions.
Intervention Type
Behavioral
Intervention Name(s)
Internet-delivered cognitive behavior therapy
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)
Treatment as usual
Intervention Description
Consist of standardized AF information that emphasizes that an active physical and social lifestyle is necessary to maintain good health, without the guidance of a psychologist or any CBT interventions.
Primary Outcome Measure Information:
Title
The Atrial Fibrillation Quality of Life (AFEQT)
Description
The AFEQT is an atrial fibrillation-specific measure that taps into the QoL-domains: symptoms, daily activities, treatment concern, and treatment satisfaction.
Time Frame
From baseline to 6 months PRIMARY ENDPOINT
Title
The Atrial Fibrillation Quality of Life (AFEQT)
Description
The AFEQT is an atrial fibrillation-specific measure that taps into the QoL-domains: symptoms, daily activities, treatment concern, and treatment satisfaction.
Time Frame
From baseline to 12 weeks
Title
The Atrial Fibrillation Quality of Life (AFEQT)
Description
The AFEQT is an atrial fibrillation-specific measure that taps into the QoL-domains: symptoms, daily activities, treatment concern, and treatment satisfaction.
Time Frame
From baseline to 9 months
Title
The Atrial Fibrillation Quality of Life (AFEQT)
Description
The AFEQT is an atrial fibrillation-specific measure that taps into the QoL-domains: symptoms, daily activities, treatment concern, and treatment satisfaction.
Time Frame
From baseline to 15 months
Secondary Outcome Measure Information:
Title
Electrocardiography (ECG) measurement
Description
Change in symptomatic burden. The patient will undergo 5 days ECG assessment in order to measure objectively symptomatic burden (number and duration of symptomatic AF episodes and symptomatic "non-AF episodes")
Time Frame
From baseline to 12 weeks
Title
ECG measurement
Description
Change in symptomatic burden. The patient will undergo 5 days ECG assessment in order to measure objectively symptomatic burden (number and duration of symptomatic AF episodes and symptomatic "non-AF episodes")
Time Frame
From baseline to 6 months
Title
ECG measurement
Description
Change in symptomatic burden. The patient will undergo 5 days ECG assessment in order to measure objectively symptomatic burden (number and duration of symptomatic AF episodes and symptomatic "non-AF episodes")
Time Frame
From baseline to 15 months
Title
Cardiac Anxiety Questionary (CAQ)
Description
Symptom preoccupation
Time Frame
From baseline to 12 weeks
Title
Cardiac Anxiety Questionary (CAQ)
Description
Symptom preoccupation
Time Frame
From baseline to 6 months
Title
Cardiac Anxiety Questionary (CAQ)
Description
Symptom preoccupation
Time Frame
From baseline to 9 months
Title
Cardiac Anxiety Questionary (CAQ)
Description
Symptom preoccupation
Time Frame
From baseline to 15 months
Title
the World Health Organization Disability Assessment Schedule (WHODAS 2.0, 12- item version)
Description
General quality of life
Time Frame
From baseline to 12 weeks
Title
WHODAS 2.0 (12-item version)
Description
General quality of life
Time Frame
From baseline to 6 months
Title
WHODAS 2.0 (12-item version)
Description
General quality of life
Time Frame
From baseline to 15 months
Title
Symptom checklist Severity and Frequency Scale (SCL)
Description
AF related symptoms
Time Frame
From baseline to 12 weeks
Title
Symptom checklist Severity and Frequency Scale (SCL)
Description
AF related symptoms
Time Frame
From baseline to 6 months
Title
Symptom checklist Severity and Frequency Scale (SCL)
Description
AF related symptoms
Time Frame
From baseline to 15 months
Title
Atrial Fibrillation Severity Scale
Description
Symptomatic burden
Time Frame
From baseline to 12 weeks
Title
Atrial Fibrillation Severity Scale
Description
Symptomatic burden
Time Frame
From baseline to 6 months
Title
Atrial Fibrillation Severity Scale
Description
Symptomatic burden
Time Frame
From baseline to 15 months
Title
Patient Health Questionnaire (PHQ-9)
Description
Depression
Time Frame
From baseline to 12 weeks
Title
PHQ-9
Description
Depression
Time Frame
From baseline to 6 months
Title
PHQ-9
Description
Depression
Time Frame
From baseline to 15 months
Title
Client satisfaction Questionnaire
Description
Treatment satisfaction
Time Frame
From baseline to 12 weeks
Title
Adverse events
Description
Potential adverse reactions to the treatment
Time Frame
From baseline to 12 weeks
Other Pre-specified Outcome Measures:
Title
Self-rated health, 1 item
Description
The measure consists of a single item that asks the participants to rate their overall health as excellent, good, fair, or poor.
Time Frame
From baseline to 12 weeks
Title
Self-rated health, 1 item
Description
The measure consists of a single item that asks the participants to rate their overall health as excellent, good, fair, or poor.
Time Frame
From baseline to 6 months
Title
Self-rated health, 1 item
Description
The measure consists of a single item that asks the participants to rate their overall health as excellent, good, fair, or poor.
Time Frame
From baseline to 15 months
Title
Healthcare consumption and work loss:Tic-P
Description
The Trimbos and Institute of Medical Technology Assessment Cost Questionnaire for Psychiatry assesses societal cost during the last month. These costs include the participant's health care consumption (direct medical costs), time spent in other health promoting activities (direct non-medical costs), and sick leave, unemployment, and reduced work capacity at work and in the domestic realm (indirect non-medical costs).
Time Frame
From baseline to 12 weeks
Title
Healthcare consumption and work loss:Tic-P
Description
The Trimbos and Institute of Medical Technology Assessment Cost Questionnaire for Psychiatry assesses societal cost during the last month. These costs include the participant's health care consumption (direct medical costs), time spent in other health promoting activities (direct non-medical costs), and sick leave, unemployment, and reduced work capacity at work and in the domestic realm (indirect non-medical costs).
Time Frame
From baseline to 6 months
Title
Healthcare consumption and work loss:Tic-P
Description
The Trimbos and Institute of Medical Technology Assessment Cost Questionnaire for Psychiatry assesses societal cost during the last month. These costs include the participant's health care consumption (direct medical costs), time spent in other health promoting activities (direct non-medical costs), and sick leave, unemployment, and reduced work capacity at work and in the domestic realm (indirect non-medical costs).
Time Frame
From baseline to 15 months
Title
The International Physical Activity Questionnaire
Description
Physical activity
Time Frame
From baseline to 6 months
Title
The International Physical Activity Questionnaire
Description
Physical activity
Time Frame
From baseline to 12 weeks
Title
The International Physical Activity Questionnaire
Description
Physical activity
Time Frame
From baseline to 9 months
Title
The International Physical Activity Questionnaire
Description
Physical activity
Time Frame
From baseline to 15 months
Title
Body Sensation Questionnaire
Description
Fear of bodily sensations
Time Frame
From baseline to 12 weeks
Title
Body Sensation Questionnaire
Description
Fear of bodily sensations
Time Frame
From baseline to 6 months
Title
Body Sensation Questionnaire
Description
Fear of bodily sensations
Time Frame
From baseline to 15 months
Title
Anxiety Sensitivity Index
Description
Anxiety sensitivity
Time Frame
From baseline to 12 weeks
Title
Anxiety Sensitivity Index
Description
Anxiety sensitivity
Time Frame
From baseline to 6 months
Title
Anxiety Sensitivity Index
Description
Anxiety sensitivity
Time Frame
From baseline to 15 months
Title
Accelerometer
Description
Objective measurement of physical activity 1 week
Time Frame
From baseline to 12 weeks
Title
Accelerometer
Description
Objective measurement of physical activity 1 week
Time Frame
From baseline to 6 months
Title
Accelerometer
Description
Objective measurement of physical activity 1 week
Time Frame
From baseline to 15 months
Title
Perceived stress scale (4-item version)
Description
Stress reactivity
Time Frame
From baseline to 12 weeks
Title
Perceived stress scale (4-item version)
Description
Stress reactivity
Time Frame
From baseline to 6 months
Title
Perceived stress scale (4-item version)
Description
Stress reactivity
Time Frame
From baseline to 9 months
Title
Perceived stress scale (4-item version)
Description
Stress reactivity
Time Frame
From baseline to 15 months

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: Inclusion criteria: A) 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) ; B) Age 18-75 years; C) On optimal medical treatment; D). Able to read and write in Swedish. Exclusion Criteria: (E) heart failure with severe systolic dysfunction (ejection fraction ≤ 35%); (F) significant valvular disease; (G) planned ablation for AF or ablation within 3 months before assessment; (H) other severe medical illness; (I) any medical restriction to physical exercise; (J) severe psychiatric disorder, severe depression, or risk of suicide; (K) alcohol dependency.
Facility Information:
Facility Name
Karolinska universitetssjukhuset Solna
City
Stockholm
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
No

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Internet-delivered Cognitive Behavior Therapy for Atrial Fibrillation

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