Anxiety Clinical Trial
Official title:
Alpha/Theta Neurofeedback Training as Treatment Method for Individuals With Moderate to Severe Trait Anxiety
| Verified date | January 2017 |
| Source | University of Hartford |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Institutional Review Board |
| Study type | Interventional |
This study evaluates if individuals with moderate to high trait anxiety can learn how to self-regulate their brain waves and reduce their trait anxiety in ten sessions of EEG alpha-theta neurofeedback training. Half of the randomly assigned participants will receive alpha/theta neurofeedback training while the other half will receive a two-part control protocol where low beta and beta waves will be uptrained in and downtrained in in successive sessions.
| Status | Completed |
| Enrollment | 28 |
| Est. completion date | January 2017 |
| Est. primary completion date | January 2017 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - adults, age 18 and above - scores of >66% on the State Trait Anxiety Inventory (STAI) Exclusion Criteria: - scores >19 on the Beck Depression Inventory (BDI-II) - scores > 9 on the Patient Health Questionnaire (PHQ-9) - comorbid diagnoses of: Major Depression, Bipolar Disorder, Schizophrenia, Substance Use Disorder, Tic disorders, Seizure Disorders |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| United States | University of Hartford | West Hartford | Connecticut |
| Lead Sponsor | Collaborator |
|---|---|
| University of Hartford |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change from baseline in the State-Trait Anxiety Inventory (STAI) Scale | Change from baseline of symptoms of anxiety to end of treatment after 4-5 weeks. The STAI scale consists of total 40 items on separate scales measuring state (20 items) and trait (20 items) anxiety. The participant reports how they feel right now at this moment for state anxiety and how they generally feel for trait anxiety. The state items are scored as: 1 (not at all), 2 (somewhat true), 3 (moderately true), 4 (very true). The trait items are scored as: 1 (almost never), 2 (sometimes), 3 (often), 4 (almost always). The total scores range from 4-80 for each scale. Higher scores indicate more anxious participants. | 1-2 weeks pre-treatment and at post treatment at end of last treatment session (4-5 weeks) | No |
| Secondary | Theta/alpha (T/A) ratios in EEG recorded at Pz scalp location | Change from baseline of T/A ratio within and between NFB session. | pre- and post each of 3 NFB segments (3 eight-minute segments per NFB session) and over the course of 10 sessions (4-5 weeks) | No |
| Secondary | 19-channel Mini-QEEG | Change in power of alpha and theta waves extracted from the QEEG. Four channels at a time are recorded (time-locked) in 5 runs for for a total 10 minutes to record all 19 channels (5 x 2 minutes) | pre-treatment and at post treatment at end of last treatment session (4-5 weeks) | No |
| Secondary | Change from baseline in Generalized Anxiety Disorder 7-item Scale (GAD-7) | Change from baseline of symptoms of anxiety to end of treatment after 4-5 weeks. | 1-2 weeks pre-treatment and at post treatment at end of last treatment session (4-5 weeks) | No |
| Secondary | Change from baseline in Beck Anxiety Inventory (BAI) Scale | Change from baseline of activation to end of treatment after 4-5 weeks. | 1-2 weeks pre-treatment and at post treatment at end of last treatment session (4-5 weeks) | No |
| Secondary | Change from baseline in Activation Deactivation Adjective Checklist (AD ACL) | Change from baseline of activation to end of treatment after 4-5 weeks. | 1-2 weeks pre-treatment and at post treatment at end of last treatment session (4-5 weeks) | No |
| Secondary | Rotter Locus of Control Scale | Correlation between internal locus of control and theta/alpha pre-and post treatment outcome. | at end of last NFB treatment session (4-5 weeks) | No |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
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