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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02739607
Other study ID # WUTimisoara-iTAD
Secondary ID
Status Recruiting
Phase N/A
First received April 12, 2016
Last updated May 5, 2016
Start date April 2016
Est. completion date March 2017

Study information

Verified date May 2016
Source West University of Timisoara
Contact Bogdan Tudor Tulbure, PhD
Phone 0040745753061
Email btulbure@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Objectives

1. To test the effectiveness and acceptability of an augmented internet-supported transdiagnostic intervention in Romania.

2. To assess the cost-effectiveness of the Internet version of the transdiagnostic program as compared to a standard treatment/usual care.


Description:

The effectiveness of a transdiagnostic intervention will be compared with a wait list control group using a randomized control trial (RCT) design in a culture where this has not been tested before. The treatment approach is mainly emotion-focus, teaching participants how to confront and experience uncomfortable emotions, and how more adaptive coping mechanisms could be used. Because internet-delivered interventions represent an effective way to disseminate evidence-based programs, investigators decided to present our intervention online.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date March 2017
Est. primary completion date September 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- be fluent in Romanian

- be over 18 years

- have the principal diagnostic of generalized anxiety disorder and/or obsessive-compulsive disorder and/or panic disorder and/or social anxiety disorder and/or major depression disorder and/or dysthymia (or any combination of these diagnostics) on Structured Clinical Interview for the Diagnostic and Statistical Manual for Mental Disorders (SCID-I)

- have access to an Internet connected computer

Exclusion Criteria:

- suicidal ideation

- ongoing psychological treatment for generalized anxiety disorder and/or obsessive-compulsive disorder and/or panic disorder and/or social anxiety disorder and/or major depression disorder and/or dysthymia

- other primary disorder that need treatment

- obstacle to participation (i.e., long travel plans)

- recent change in psychiatric medication (i.e., during the last 6 weeks)

Study Design


Intervention

Behavioral:
Transdiagnostic program
This transdiagnostic program is based on the general Cognitive Behavioral Therapy (CBT) principles and targets core higher order factors such as negative affectivity and emotion dysregulation, using common intervention techniques applicable across disorders. The program was designed to directly address the aversive emotional experiences often reported by clients, hoping to reverse participants' maladaptive thinking style and dysfunctional behaviors.

Locations

Country Name City State
Romania West University of Timisoara Timi?oara Timi?

Sponsors (1)

Lead Sponsor Collaborator
West University of Timisoara

Country where clinical trial is conducted

Romania, 

Outcome

Type Measure Description Time frame Safety issue
Primary Penn State Worry Questionnaire (PSWQ) The PSWQ was designed to measure participant's level of generalized anxiety or worry. The scale is unidimensional and the total score rages from 16 to 80. Low scores are associated with low levels of worry, while high scores are associated with high levels of worry. Absolute values (average score) of PSWQ at 11 weeks (post-intervention)
Primary Social Phobia Inventory (SPIN) The SPIN was designed to measure participant's level of social phobia. The scale is unidimensional and the total score rages from 0 to 68. Low scores are associated with low levels of social phobia, while high scores are associated with high levels of social phobia. Absolute values (average score) of SPIN at 11 weeks (post-intervention)
Primary Yale-Brown Obsessive Compulsive Scale (YBOCS) The YBOCS was designed to measure participant's level of obsessions and compulsions (O&C). The scale total score rages from 0 to 40. Low scores are associated with low levels of O&C, while high scores are associated with high levels of O&C. Absolute values (average score) of YBOCS at 11 weeks (post-intervention)
Primary Panic Disorder Severity Scale - Self Report (PDSS-SR) The PDSS-SR was designed to measure participant's level of panic. The scale is unidimensional and the total score rages from 0 to 28. Low scores are associated with low levels of panic, while high scores are associated with high levels of panic. Absolute values (average score) of PDSS-SR at 11 weeks (post-intervention)
Primary Post-Traumatic Stress Disorder Checklist for the Diagnostic and Statistical Manual-5 (PCL-5) The PCL-5 was designed to measure participant's level of post-traumatic stress. The scale is unidimensional and the total score rages from 0 to 80. Low scores are associated with low levels of post-traumatic stress, while high scores are associated with high levels of post-traumatic stress. Absolute values (average score) of PCL-5 at 11 weeks (post-intervention)
Primary Beck Depression Inventory-II (BDI-II) The Beck Depression Inventory-II (BDI-II) was designed to measure participant's level of depression. The scale is unidimensional and the total score rages from 0 to 63. Low scores are associated with low levels of depression, while high scores are associated with high levels of depression. Absolute values (average score) of BDI-II at 11 weeks (post-intervention)
Secondary Emotion Regulation Questionnaire (ERQ) The ERQ was designed to measure participant's level of emotion regulation. The scale is multidimensional and measures two emotion regulation strategies: reappraisal and suppression. Low scores are associated with low levels of emotion regulation, while high scores are associated with high levels of emotion regulation. Absolute values (average score) of ERQ at 11 weeks (post-intervention)
Secondary Anxiety Sensitivity Index (ASI) The ASI was designed to measure participant's level of anxiety sensitivity. The scale is unidimensional and the total score rages from 0 to 64. Low scores are associated with low levels of anxiety sensitivity, while high scores are associated with high levels of anxiety sensitivity. Absolute values (average score) of ASI at 11 weeks (post-intervention)
Secondary Beck Anxiety Inventory (BAI) The BAI was designed to measure participant's level of anxiety. The scale is unidimensional and the total score rages from 0 to 63. Low scores are associated with low levels of anxiety, while high scores are associated with high levels of anxiety. Absolute values (average score) of Treatment satisfaction and acceptability at 11 weeks (post-intervention)
Secondary Almost Perfect Scale-Revised (APS-R) The APS-R was designed to measure participant's level of perfectionism. The scale is multidimensional and measures three dimensions of perfectionism: high standards, order and discrepancy. Low scores are associated with low levels of perfectionism, while high scores are associated with high levels of perfectionism. Absolute values (average score) of APS-R at 11 weeks (post-intervention)
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