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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06267313
Other study ID # 2023-078-PAU
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 19, 2024
Est. completion date February 19, 2027

Study information

Verified date April 2024
Source Palo Alto University
Contact Mikael Rubin, PhD
Phone 650-433-3805
Email mrubin@paloaltou.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aims to test whether attention training (attention bias modification or attention control training) reduces distress or COVID-19 related anxiety compared to a neutral condition.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date February 19, 2027
Est. primary completion date February 19, 2027
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - COVID-19 Anxiety Syndrome Scale > 7 and/or COVID-19 related loss Exclusion Criteria: - Does not speak English Fluently

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Attention Bias Modification
Training attention away from threat
Attention Control Training
Training attention control
Neutral training
Attention training with Neutral stimuli

Locations

Country Name City State
United States Palo Alto University Palo Alto California

Sponsors (1)

Lead Sponsor Collaborator
Palo Alto University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary COVID-19 Anxiety Syndrome Scale The measure is scored using a 5-point time anchored scale (0 = Not at all to 4 = Nearly every day over the last 2 weeks) and scores range between 0 and 20, with higher scores reflecting worse outcome. 0 days
Primary COVID-19 Anxiety Syndrome Scale The measure is scored using a 5-point time anchored scale (0 = Not at all to 4 = Nearly every day over the last 2 weeks) and scores range between 0 and 20, with higher scores reflecting worse outcome. 21 days
Primary COVID-19 Anxiety Syndrome Scale The measure is scored using a 5-point time anchored scale (0 = Not at all to 4 = Nearly every day over the last 2 weeks) and scores range between 0 and 20, with higher scores reflecting worse outcome. 49 days
Primary COVID-19 Anxiety Syndrome Scale The measure is scored using a 5-point time anchored scale (0 = Not at all to 4 = Nearly every day over the last 2 weeks) and scores range between 0 and 20, with higher scores reflecting worse outcome. 105 days
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