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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05297838
Other study ID # 64860
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 25, 2022
Est. completion date January 26, 2023

Study information

Verified date August 2023
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness of different technologies, in particular Virtual Reality, inclusive of passive content, active content, cognitive load modulation, and positive encouragement coaching to increase the pain threshold as assessed by immersing a hand in ice water while utilizing a stationary bike.


Recruitment information / eligibility

Status Completed
Enrollment 151
Est. completion date January 26, 2023
Est. primary completion date January 26, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Greater than 18 years of age - English speaking - Hearing intact Exclusion Criteria: - Patients who do not consent - Are currently taking beta blockers or other chronotropic heart medication(s) - Have a history of severe motion sickness - Currently have nausea - Currently experiencing seizures - Are clinically unstable

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Stationary Bike
Stationary Bike while hand is submerged in ice bath
Virtual Reality (VR) Headset
VR headset containing gameplay
Ice Bath
Pain was elicited via a cold pressor test, which is an established method of producing controlled and repeatable painful stimuli in an experimental setting

Locations

Country Name City State
United States Lucile Packard Children's Hospital Stanford Palo Alto California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Self-Reported Pain Scores (Ice Bath vs VR Bike) Pain Scores will be collected during ice bath (maximum of 4 minutes) every 30 seconds via numeric rating scale (NRS), 0 being no pain, 10 being worst pain imaginable Duration of ice bath (approximately 0 - 4 minutes)
Primary Sympathetic Activation (VR vs VR Bike) Assessed via the electrodermal activity (EDA biosensor), which recorded skin conductance response density (SCRD) data in 30 second epochs. SCRD was recorded for the duration of the cold pressor test and one minute before and after submersion. The same primary and secondary outcome measures were collected at identical time points during the different cold pressor challenges on each hand Duration of ice bath (approximately 0 - 4 minutes)
Secondary Pain Tolerance (Ice Bath vs VR Bike) Defined by time of hand removal from the ice bath in seconds. 4 minute maximum. Duration of ice bath (approximately 0 - 4 minutes)
Secondary Sympathetic Activation (Ice Bath vs VR Bike) Assessed via the electrodermal activity (EDA biosensor), which recorded skin conductance response density (SCRD) data in 30 second epochs. SCRD was recorded for the duration of the cold pressor test and one minute before and after submersion. The same primary and secondary outcome measures were collected at identical time points during the different cold pressor challenges on each hand. Duration of ice bath (approximately 0 - 4 minutes)
Secondary Self-Reported Pain Scores (VR vs VR Bike) Pain Scores will be collected during ice bath (maximum of 4 minutes) every 30 seconds via numeric rating scale (NRS), 0 being no pain, 10 being worst pain imaginable and immediately after participant removed their hand from ice bath. Duration of ice bath (approximately 0 - 4 minutes)
Secondary Pain Tolerance (VR vs VR Bike) Defined by time of hand removal from the ice bath in seconds. 4 minute maximum. The same outcome measure were collected at identical timepoints during both conditions. Duration of ice bath (approximately 0 - 4 minutes)
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