Trial Outcomes & Findings for Impact of Virtual Reality on Pre-procedural anxieTy Prior to Heart cathEterIzAtion - VR-THEIA (NCT NCT03662607)
NCT ID: NCT03662607
Last Updated: 2026-04-14
Results Overview
The primary outcome of this study is patient anxiety, as measured by the State Trait Anxiety Inventory (STAI) score. STAI is a psychological inventory consisting of 40 self-report items on a 4-point Likert scale. The STAI measures two types of anxiety - state anxiety and trait anxiety. Scores range from 20 to 80, with higher scores correlating with greater anxiety.
COMPLETED
NA
180 participants
Change from baseline visit to procedure day. Baseline visits will occur up to 4 weeks prior to procedure.
2026-04-14
Participant Flow
Participant milestones
| Measure |
Control
Standard preprocedural education
|
VR Group (Treatment)
Stanard preprocedural education plus viewing of virtual reality video
|
|---|---|---|
|
Overall Study
STARTED
|
91
|
89
|
|
Overall Study
COMPLETED
|
91
|
89
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Race and Ethnicity were not collected from any participant.
Baseline characteristics by cohort
| Measure |
Control
n=91 Participants
Standard preprocedural education
|
VR Group (Treatment)
n=89 Participants
Standard preprocedural education plus viewing of virtual reality video
|
Total
n=180 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=91 Participants
|
0 Participants
n=89 Participants
|
0 Participants
n=180 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
46 Participants
n=91 Participants
|
42 Participants
n=89 Participants
|
88 Participants
n=180 Participants
|
|
Age, Categorical
>=65 years
|
45 Participants
n=91 Participants
|
47 Participants
n=89 Participants
|
92 Participants
n=180 Participants
|
|
Age, Continuous
|
64 years
STANDARD_DEVIATION 8.52 • n=91 Participants
|
64 years
STANDARD_DEVIATION 8 • n=89 Participants
|
64 years
STANDARD_DEVIATION 8 • n=180 Participants
|
|
Sex: Female, Male
Female
|
30 Participants
n=91 Participants
|
35 Participants
n=89 Participants
|
65 Participants
n=180 Participants
|
|
Sex: Female, Male
Male
|
61 Participants
n=91 Participants
|
54 Participants
n=89 Participants
|
115 Participants
n=180 Participants
|
|
Race and Ethnicity Not Collected
|
—
|
—
|
0 Participants
Race and Ethnicity were not collected from any participant.
|
|
Region of Enrollment
United States
|
91 Participants
n=91 Participants
|
89 Participants
n=89 Participants
|
180 Participants
n=180 Participants
|
PRIMARY outcome
Timeframe: Change from baseline visit to procedure day. Baseline visits will occur up to 4 weeks prior to procedure.The primary outcome of this study is patient anxiety, as measured by the State Trait Anxiety Inventory (STAI) score. STAI is a psychological inventory consisting of 40 self-report items on a 4-point Likert scale. The STAI measures two types of anxiety - state anxiety and trait anxiety. Scores range from 20 to 80, with higher scores correlating with greater anxiety.
Outcome measures
| Measure |
Control
n=91 Participants
Standard preprocedural education
|
VR Group (Treatment)
n=89 Participants
Standard preprocedural education plus viewing of virtual reality video
|
|---|---|---|
|
Change in Anxiety Measured by the Sate-Trait Anxiety Inventory (STAI)
|
69.81 Mean STAI score
Standard Deviation 17.11
|
65.71 Mean STAI score
Standard Deviation 15.22
|
Adverse Events
Control
Treatment
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place