Trials / Completed
CompletedNCT03346239
Effect of Attention Training or SSRIs on Symptoms and Neural Activation in Social Anxiety
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 105 (actual)
- Sponsor
- Tel Aviv University · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the clinical efficacy and neuro-cognitive mechanisms of Gaze-Contingent Usic Reward Therapy for social anxiety disorder, compared with treatment with SSRIs or waitlist control.
Detailed description
Attention biases in threat processing have been assigned a prominent role in the etiology and maintenance of anxiety disorders. The purpose of this study is to determine whether giving gaze-contingent feedback is an effective treatment for social anxiety disorder, compared to treatment with SSRI (Escitelopram) and a waitlist control. A secondary purpose is to explore the unique neuro-cognitive mechanisms of this treatment, using eye-tracking, MRI and fMRI measurements. Participants will be assessed using clinical interviews and self-rated questionnaires before, during and after 12 weeks of treatment or wait. Outcome measures will be social anxiety symptoms, as well as dwell time on threat in eye-tracking paradigms tested in previous studies, and BOLD signals in MRI measurements. Neuro-cognitive mechanisms will be explored as potential mediators of clinical efficacy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | Gaze Contingent Music Reward Therapy | Feedback according to participants' viewing patterns, in order to modify their attention. |
| DRUG | Escitalopram | 10-20 mg of Escitalopram |
| BEHAVIORAL | Waitlist | Participants will wait for 12 weeks while in touch with the clinic, then receive GC-MRT for 8 weeks. |
Timeline
- Start date
- 2018-07-20
- Primary completion
- 2021-12-01
- Completion
- 2021-12-01
- First posted
- 2017-11-17
- Last updated
- 2022-02-01
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT03346239. Inclusion in this directory is not an endorsement.