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Attention, Teleconferencing and Social Anxiety

Investigating Attentional Processes: Teleconferencing and Social Anxiety

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04729803
Enrollment
53
Registered
2021-01-29
Start date
2021-01-18
Completion date
2022-06-30
Last updated
2024-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Social Anxiety Disorder

Brief summary

This study involves completing some online assessments and an intervention for social anxiety that all involve interactions with other people on a teleconferencing call.

Interventions

BEHAVIORALExperimental: Attention Guidance + Exposure

1. Participants will receive a brief standardized psychoeducation module, presented via a video recording. 2. Participants will then complete up to 10 analogue teleconferencing calls, each lasting a maximum of two minutes. 3. Between speeches participants will have a 1-minute break. 4. Participants will complete the subjective units of distress scale (SUDS) before and after each speech trial. The experimental attention guidance condition: (1) the intervention rationale will include information about the importance of visually attending to the faces of the audience; (2) participants will be given target audience members to focus their gaze on during the their impromptu response. They will be told that they should look at and focus on the target audience member for the whole response.

BEHAVIORALActive Comparator: Exposure Alone

1. Participants will receive a brief standardized psychoeducation module, presented via a video recording. 2. Participants will then complete up to 10 analogue teleconferencing calls, each lasting a maximum of two minutes. 3. Between speeches participants will have a 1-minute break. 4. Participants will complete the subjective units of distress scale (SUDS) before and after each speech trial.

BEHAVIORALExperimental: Attention Control + Exposure

1. Participants will receive a brief standardized psychoeducation module, presented via a video recording. F 2. Participants will then complete up to 10 analogue teleconferencing calls, each lasting a maximum of two minutes. During each call participants will be prompted by one of the audience members. 3. Between speeches participants will have a 1-minute break. 4. Participants will complete the subjective units of distress scale (SUDS) before and after each speech trial. The experimental attention control condition: (1) the intervention rationale will include information about the importance of attention control; (2) participants will be given target at the center of the screen to focus their gaze on during the their impromptu response. They will be told that they should look at and focus on the target for the whole response.

Sponsors

University of Texas at Austin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-75 * Fluent in English because the data collection materials have not yet been standardized in other languages * Having access to a computer with a webcam and ability to record audio * Personal Report of Communication Apprehension \> 80 * Leibowitz Social Anxiety Scale \> 30 * Meets DSM-5 Criteria for Social Anxiety Disorder

Exclusion criteria

* Significant visual impairment precluding the use of the eye tracking equipment * Current, or history of bipolar disorder; current, or history of psychosis

Design outcomes

Primary

MeasureTime frameDescription
Personal Report of Communication Apprehension Questionnaireprior to the first treatment session, an average of 2 daysAssessment of communication concerns, range of scores is 24-120; higher scores are worse
Leibowitz Social Anxiety Scale Questionnaireprior to the first treatment session, an average of 2 daysAssessment of general social anxiety, range of scores is 0-144; higher scores are worse

Countries

United States

Participant flow

Participants by arm

ArmCount
Attention Guidance + Exposure
Participants will complete teleconferencing-based exposure trials with an attention guidance component. Experimental: Attention Guidance + Exposure: 1) Participants will receive a brief standardized psychoeducation module, presented via a video recording. 2\) Participants will then complete up to 10 analogue teleconferencing calls, each lasting a maximum of two minutes. 3\) Between speeches participants will have a 1-minute break. 4) Participants will complete the subjective units of distress scale (SUDS) before and after each speech trial. The experimental attention guidance condition: (1) the intervention rationale will include information about the importance of visually attending to the faces of the audience; (2) participants will be given target audience members to focus their gaze on during the their impromptu response. They will be told that they should look at and focus on the target audience member for the whole response.
13
Exposure Alone
Participants will complete teleconferencing-based exposure trials. Active Comparator: Exposure Alone: 1) Participants will receive a brief standardized psychoeducation module, presented via a video recording. 2\) Participants will then complete up to 10 analogue teleconferencing calls, each lasting a maximum of two minutes. 3\) Between speeches participants will have a 1-minute break. 4) Participants will complete the subjective units of distress scale (SUDS) before and after each speech trial.
18
Attention Control + Exposure
Participants will complete teleconferencing-based exposure trials with an attention control component. Experimental: Attention Control + Exposure: 1) Participants will receive a brief standardized psychoeducation module, presented via a video recording. F 2) Participants will then complete up to 10 analogue teleconferencing calls, each lasting a maximum of two minutes. During each call participants will be prompted by one of the audience members. 3\) Between speeches participants will have a 1-minute break. 4) Participants will complete the subjective units of distress scale (SUDS) before and after each speech trial. The experimental attention control condition: (1) the intervention rationale will include information about the importance of attention control; (2) participants will be given target at the center of the screen to focus their gaze on during the their impromptu response. They will be told that they should look at and focus on the target for the whole response.
22
Total53

Baseline characteristics

CharacteristicTotalAttention Guidance + ExposureExposure AloneAttention Control + Exposure
Age, Continuous19.13 years
STANDARD_DEVIATION 1.44
19.20 years
STANDARD_DEVIATION 1.52
18.70 years
STANDARD_DEVIATION 1.02
19.5 years
STANDARD_DEVIATION 1.77
Ethnicity (NIH/OMB)
Hispanic or Latino
20 Participants5 Participants8 Participants7 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
33 Participants8 Participants10 Participants15 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
11 Participants3 Participants2 Participants6 Participants
Race (NIH/OMB)
Black or African American
2 Participants0 Participants1 Participants1 Participants
Race (NIH/OMB)
More than one race
13 Participants4 Participants6 Participants3 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
7 Participants0 Participants3 Participants4 Participants
Race (NIH/OMB)
White
20 Participants6 Participants6 Participants8 Participants
Region of Enrollment
United States
53 participants13 participants18 participants22 participants
Sex: Female, Male
Female
46 Participants13 Participants17 Participants16 Participants
Sex: Female, Male
Male
7 Participants0 Participants1 Participants6 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
0 / 180 / 220 / 13
other
Total, other adverse events
0 / 180 / 220 / 13
serious
Total, serious adverse events
0 / 180 / 220 / 13

Outcome results

Primary

Leibowitz Social Anxiety Scale Questionnaire

Assessment of general social anxiety, range of scores is 0-144; higher scores are worse

Time frame: prior to the first treatment session, an average of 2 days

ArmMeasureValue (MEAN)Dispersion
Exposure AloneLeibowitz Social Anxiety Scale Questionnaire81.06 score on a scaleStandard Deviation 13.4
Attention Control + ExposureLeibowitz Social Anxiety Scale Questionnaire74.50 score on a scaleStandard Deviation 13.94
Attention Guidance + ExposureLeibowitz Social Anxiety Scale Questionnaire87.77 score on a scaleStandard Deviation 19.93
Primary

Leibowitz Social Anxiety Scale Questionnaire

Assessment of general social anxiety, range of scores is 0-144; higher scores are worse

Time frame: 1-week follow-up

ArmMeasureValue (MEAN)Dispersion
Exposure AloneLeibowitz Social Anxiety Scale Questionnaire77.99 score on a scaleStandard Deviation 23.6
Attention Control + ExposureLeibowitz Social Anxiety Scale Questionnaire57.70 score on a scaleStandard Deviation 19.24
Attention Guidance + ExposureLeibowitz Social Anxiety Scale Questionnaire71.00 score on a scaleStandard Deviation 26
Primary

Leibowitz Social Anxiety Scale Questionnaire

Assessment of general social anxiety, range of scores is 0-144; higher scores are worse

Time frame: 2-week follow-up

ArmMeasureValue (MEAN)Dispersion
Exposure AloneLeibowitz Social Anxiety Scale Questionnaire81.67 score on a scaleStandard Deviation 23.52
Attention Control + ExposureLeibowitz Social Anxiety Scale Questionnaire50.13 score on a scaleStandard Deviation 15.72
Attention Guidance + ExposureLeibowitz Social Anxiety Scale Questionnaire71.00 score on a scaleStandard Deviation 30.91
Primary

Personal Report of Communication Apprehension Questionnaire

Assessment of communication concerns, range of scores is 24-120; higher scores are worse

Time frame: prior to the first treatment session, an average of 2 days

ArmMeasureValue (MEAN)Dispersion
Exposure AlonePersonal Report of Communication Apprehension Questionnaire88.06 score on a scaleStandard Deviation 11.66
Attention Control + ExposurePersonal Report of Communication Apprehension Questionnaire87.64 score on a scaleStandard Deviation 11.91
Attention Guidance + ExposurePersonal Report of Communication Apprehension Questionnaire95.69 score on a scaleStandard Deviation 14.35
Primary

Personal Report of Communication Apprehension Questionnaire

Assessment of communication concerns, range of scores is 24-120; higher scores are worse

Time frame: 1-week follow-up

ArmMeasureValue (MEAN)Dispersion
Exposure AlonePersonal Report of Communication Apprehension Questionnaire70.71 score on a scaleStandard Deviation 7.01
Attention Control + ExposurePersonal Report of Communication Apprehension Questionnaire65.90 score on a scaleStandard Deviation 5.36
Attention Guidance + ExposurePersonal Report of Communication Apprehension Questionnaire70.00 score on a scaleStandard Deviation 1.1
Primary

Personal Report of Communication Apprehension Questionnaire

Assessment of communication concerns, range of scores is 24-120; higher scores are worse

Time frame: 2-week follow-up

ArmMeasureValue (MEAN)Dispersion
Exposure AlonePersonal Report of Communication Apprehension Questionnaire70.25 score on a scaleStandard Deviation 6.25
Attention Control + ExposurePersonal Report of Communication Apprehension Questionnaire67.13 score on a scaleStandard Deviation 3.23
Attention Guidance + ExposurePersonal Report of Communication Apprehension Questionnaire71.00 score on a scaleStandard Deviation 1.67

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026