ACT-smart: Smartphone-supplemented iCBT for Social Phobia and/or Panic Disorder
Primary Purpose
Panic Disorder, Phobic Disorders
Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Smartphone-supplemented iCBT
Therapist support
Active waiting list
Sponsored by
About this trial
This is an interventional treatment trial for Panic Disorder
Eligibility Criteria
Inclusion Criteria:
- Satisfy DSM-IV-TR criteria for panic disorder and/or social anxiety disorder as assessed by the SCID.
- Daily access to the Internet via computer and smartphone
- Residing in Sweden and speaking sufficient Swedish to communicate with the research team
Exclusion Criteria:
- Parallel psychological treatment
- Non-stable dosage of psychoactive medication during last 3 months
- Participants deemed to suffer from suicidal tendencies or another condition requiring specialized treatment
Sites / Locations
- Stockholm University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Active Comparator
Arm Label
Smartphone-supplemented iCBT with therapist support
Smartphone-supplemented iCBT without therapist support
Active waiting list control group with delayed treatment
Arm Description
n = 50
n = 50
n = 50
Outcomes
Primary Outcome Measures
The Generalised Anxiety Disorder 7-item (GAD-7)
The Generalised Anxiety Disorder 7-item (GAD-7). The 7 items of the scales are rated 0-3 ("Not at all" to "Nearly every day") based on their occurrence within the last 2 weeks. Good internal consistency and factor structure has been reported.
Secondary Outcome Measures
Self-rated Liebowitz Social Anxiety Scale (LSAS-SR)
Self-rated Panic Disorder Severity Scale (PDSS-SR)
9-item Patient Health Questionnaire (PHQ-9)
Quality of Life Inventory (QOLI)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01963806
Brief Title
ACT-smart: Smartphone-supplemented iCBT for Social Phobia and/or Panic Disorder
Official Title
Guided and Unguided CBT for Social Anxiety Disorder and/or Panic Disorder Via the Internet and a Smartphone Application
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
September 2013 (undefined)
Primary Completion Date
November 2015 (Actual)
Study Completion Date
November 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stockholm University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
BACKGROUND: Smartphone technology presents a novel and promising opportunity to extend the reach of psychotherapeutic interventions by moving selected parts of the therapy into the real-life situations causing distress. This randomised controlled trial will investigate the effect of a transdiagnostic, Internet-administered cognitive behavioural (iCBT) self-help program for anxiety, supplemented with a tailored smartphone application. The effect of added therapist support will also be studied.
METHODS/DESIGN: 150 participants meeting diagnostic criteria for social anxiety disorder and/or panic disorder will be evenly randomised to one of three treatment arms: (1) smartphone-supplemented iCBT with therapist support; (2) smartphone-supplemented iCBT without therapist support; or (3) an active waiting list control group with delayed treatment. After the 10 week treatment period, the control group (3) will receive the same treatment as group (2). Primary outcome measure will be the Generalised Anxiety Disorder 7-item self-rating scale. Secondary measures include other anxiety, depression and quality of life measures. In addition to pre- and post-treatment measurements, the study includes two mid-treatment and two follow-up assessments (12 and 24 months).
HYPOTHESES: Based on prior research, we hypothesise that the therapist-guided form will be superior to the unguided form in reducing anxiety levels, and that both delivery modes will be superior to an active waiting-list control group.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Panic Disorder, Phobic Disorders
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
152 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Smartphone-supplemented iCBT with therapist support
Arm Type
Experimental
Arm Description
n = 50
Arm Title
Smartphone-supplemented iCBT without therapist support
Arm Type
Experimental
Arm Description
n = 50
Arm Title
Active waiting list control group with delayed treatment
Arm Type
Active Comparator
Arm Description
n = 50
Intervention Type
Behavioral
Intervention Name(s)
Smartphone-supplemented iCBT
Intervention Description
The Internet-administered cognitive behavioural self-help program (iCBT) will be divided into 10 weekly, progressively available modules covering CBT and Acceptance and Commitment Therapy (ACT) conceptualisations of anxiety disorders, as well as more specific therapeutic techniques such as cognitive restructuring, exposure training, attention and breathing exercises and relapse prevention . Each module also includes writing exercises.
Also included is a tailored smartphone application. Briefly, the application allows the user to access, create and modify a personal database of behaviours and check-off these behaviours immediately when completed. Frequency of carried-out behaviours are recorded and displayed as statistics. The application also allows users to browse and search a database of behaviours uploaded by other study participants, providing both inspiration and a sense of social support.
Intervention Type
Behavioral
Intervention Name(s)
Therapist support
Intervention Description
The role of the therapists will be to provide feedback on the written exercises of each treatment module, as well as to provide support and encouragement. As a rule of thumb, the therapists will devote 15 minutes per participant and week.
Intervention Type
Other
Intervention Name(s)
Active waiting list
Intervention Description
Completes measurements at day 24 and 48 and at the end of the initial treatment period, otherwise no activity until crossover.
Primary Outcome Measure Information:
Title
The Generalised Anxiety Disorder 7-item (GAD-7)
Description
The Generalised Anxiety Disorder 7-item (GAD-7). The 7 items of the scales are rated 0-3 ("Not at all" to "Nearly every day") based on their occurrence within the last 2 weeks. Good internal consistency and factor structure has been reported.
Time Frame
Change from baseline at: [1] day 24 and [2] day 48 into the 10-week treatment period; [3] 0-1 week after the treatment period; follow-ups at [4] month 12 and [5] month 36 after the treatment period.
Secondary Outcome Measure Information:
Title
Self-rated Liebowitz Social Anxiety Scale (LSAS-SR)
Time Frame
Change from baseline at: [1] 0-1 week after the treatment period; follow-ups at [2] month 12 and [3] month 36 after the treatment period.
Title
Self-rated Panic Disorder Severity Scale (PDSS-SR)
Time Frame
Change from baseline at: [1] 0-1 week after the treatment period; follow-ups at [2] month 12 and [3] month 36 after the treatment period.
Title
9-item Patient Health Questionnaire (PHQ-9)
Time Frame
Change from baseline at: [1] day 24 and [2] day 48 into the 10-week treatment period; [3] 0-1 week after the treatment period; follow-ups at [4] month 12 and [5] month 36 after the treatment period.
Title
Quality of Life Inventory (QOLI)
Time Frame
Change from baseline at: [1] 0-1 week after the treatment period; follow-ups at [2] month 12 and [3] month 36 after the treatment period.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Satisfy DSM-IV-TR criteria for panic disorder and/or social anxiety disorder as assessed by the SCID.
Daily access to the Internet via computer and smartphone
Residing in Sweden and speaking sufficient Swedish to communicate with the research team
Exclusion Criteria:
Parallel psychological treatment
Non-stable dosage of psychoactive medication during last 3 months
Participants deemed to suffer from suicidal tendencies or another condition requiring specialized treatment
Facility Information:
Facility Name
Stockholm University
City
Stockholm
Country
Sweden
12. IPD Sharing Statement
Citations:
PubMed Identifier
24351088
Citation
Lindner P, Ivanova E, Ly KH, Andersson G, Carlbring P. Guided and unguided CBT for social anxiety disorder and/or panic disorder via the Internet and a smartphone application: study protocol for a randomised controlled trial. Trials. 2013 Dec 18;14:437. doi: 10.1186/1745-6215-14-437.
Results Reference
derived
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ACT-smart: Smartphone-supplemented iCBT for Social Phobia and/or Panic Disorder
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