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Clinical Trial Summary

In this randomized, double-blind, controlled, parallel group study (conducted over 12-months), enrollment is expected of up to 60 subjects (30 men and 30 women) ages 18+ who are currently going through withdrawal of OUD and being treated at local substance abuse clinics. The study visits will include screening, baseline, Weeks 1, 2, 3, and 4, with both safety and efficacy assessments.

Clinical Trial Description

Approximate time commitment is 30 minutes / day, for 5 days / week, in testing effects of specialized 'massage' chair for a period of 4 weeks (up to total 20 treatment periods). Only about 20 minutes time is in the test chair, and the rest is setup time and completing questionnaires. - Upon arrival to the clinic for treatment, some short questions are asked. - Participant is seated in a HWBV chair device. - A clip is attached to one finger to track heart rate and skin response to the treatment. - After relaxing for about 5 minutes, the HWBV chair actuated for 10 minutes. - The finger attachment is disconnected. - Post-treatment, some more survey questions conclude the session. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT05056753
Study type Interventional
Source PhotoPharmics, Inc.
Contact Dan Adams
Phone +1-801-770-6960
Email [email protected]
Status Recruiting
Phase N/A
Start date October 2021
Completion date June 2022

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