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Clinical Trial Summary

This is a prospective study looking at the impact of psychosensory therapy and how it can diminish pain and consumption of pain medications. The primary study objective is to evaluate the change in Visual Analogue Score (VAS) score assessing for pain from Baseline, every day of inpatient stay, 7 days after leaving hospital (via phone), and 3 months post-op(via phone) and to correlate the psychosensory therapy and overall use of pain medications/narcotics.


Clinical Trial Description

The study will aim to enroll 50 subjects. 25 subjects will receive placebo therapy which will be dummy movements while the other 25 will receive psychosensory therapy. The treatment group will involve a touch technique called havening. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02765932
Study type Interventional
Source New York University School of Medicine
Contact
Status Completed
Phase N/A
Start date June 2016
Completion date March 5, 2018

See also
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