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Clinical Trials/NCT03845101
NCT03845101
Recruiting
Not Applicable

SoREAL- a Randomized Clinical Trial

Mental Health Services in the Capital Region, Denmark5 sites in 1 country302 target enrollmentFebruary 19, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Social Anxiety Disorder
Sponsor
Mental Health Services in the Capital Region, Denmark
Enrollment
302
Locations
5
Primary Endpoint
Change in symptom severity of primary diagnosis
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

Introduction: Anxiety disorders have a high lifetime prevalence, early-onset, and long duration or chronicity. Exposure therapy is considered one of the most effective elements in cognitive behavioral therapy (CBT) for anxiety, but in vivo exposure can be challenging to access and control, and is sometimes rejected by patients because they consider it too aversive. Virtual reality allows flexible and controlled exposure to challenging situations in an immersive and protected environment.

Aim: The SoREAL-trial aims to investigate the effect of group cognitive-behavioral therapy (CBT-in vivo) versus group cognitive behavioral therapy with virtual reality exposure (CBT-in virtuo) for patients diagnosed with social anxiety disorder and/or agoraphobia, in mixed groups.

Methods & Analysis: The design is an investigator-initiated randomized, assessor-blinded, parallel-group and superiority-designed clinical trial. Three hundred two patients diagnosed with social anxiety disorder and/or agoraphobia will be included from the regional mental health centers of Copenhagen and North Sealand and the Northern Region of Denmark. All patients will be offered a manual-based 14-week cognitive behavioral group treatment program, including eight sessions with exposure therapy. Therapy groups will be centrally randomized with concealed allocation sequence to either CBT-in virtuo or CBT-in vivo. Patients will be assessed at baseline, post-treatment and one-year follow-up by treatment blinded researchers and research assistants. The primary outcome will be diagnosis-specific symptoms measured with the Liebowitz Social Anxiety Scale for patients with social anxiety disorder and the Mobility Inventory for Agoraphobia for patients with agoraphobia. Secondary outcome measures will include depression symptoms, social functioning, and patient satisfaction. Exploratory outcomes will be substance and alcohol use, working alliance and quality of life.

Ethics and dissemination: The trial has been approved by the research ethics committee in the Capital Region of Denmark. All results, positive, negative as well as inconclusive, will be published as quickly as possible and still in concordance with Danish law on the protection of confidentially and personal information. Results will be presented at national and international scientific conferences.

Registry
clinicaltrials.gov
Start Date
February 19, 2019
End Date
April 9, 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Mental Health Services in the Capital Region, Denmark
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Fulfilling diagnostic criteria for social anxiety disorder (ICD-code: F40.1) and/or Agoraphobia (ICD-code: 40.0)
  • Age 18-75 years
  • Sufficient knowledge of the Danish language
  • Informed consent

Exclusion Criteria

  • Alcohol or drug dependence (ICD-code: F10-19.20-26).

Outcomes

Primary Outcomes

Change in symptom severity of primary diagnosis

Time Frame: Between 30 to 1 day(s) before treatment, between 0 and 14 days after treatment ends and between 365 to 395 days after first assesment.

Total scores on the Liebowitz Social Anxiety Scale (LSAS) for patients with social anxiety disorder and the Mobility Inventory for Agoraphobia (MIA) for patients with Agoraphobia measured pre-treatment, post-treatment and at one-year follow-up converted to the 'Percentage of Maximum Possible Score' (POMP) and averaged within treatment arms. POMP calculations can bring differently measured items to the same metric and do not change the multivariate distribution and covariance matrix of the transformed variables. Ranges from 0 to 100. Higher is worse.

Secondary Outcomes

  • Change in Work and Social Adjustment Scale score(Between 30 to 1 day(s) before treatment, between 0 and 14 days after treatment ends and between 365 to 395 days after first assesment.)
  • Treatment response on agoraphobia symptoms(Between 0 and 14 day(s) after treatment ends and between 365 to 395 days after first assesment.)
  • Remission from social anxiety disorder(Between 0 and 14 day(s) after treatment ends and between 365 to 395 days after first assesment.)
  • Change in Brief Version of the Fear of Negative Evaluation Scale score(Between 30 to 1 day(s) before treatment, between 0 and 14 days after treatment ends and between 365 to 395 days after first assesment.)
  • Client Satisfaction Questionnaire(Measured between 0 and 14 days after treatment ends)
  • Change in WHO Well-Being Index 5 items, score(Between 30 to 1 day(s) before treatment, between 0 and 14 day(s) after treatment ends and between 365 to 395 days after first assesment.)
  • Remission from agoraphobia(Between 0 and 14 day(s) after treatment ends and between 365 to 395 days after first assesment.)
  • Change in Hamilton Depression Rating Scale, 6 item score(Between 30 to 1 day(s) before treatment, between 0 and 14 days after treatment ends and between 365 to 395 days after first assesment.)
  • Treatment response on social anxiety disorder symptoms(Between 0 and 14 day(s) after treatment ends and between 365 to 395 days after first assesment.)

Study Sites (5)

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