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Clinical Trial Summary

The purpose of this study is to determine the potential efficacy and feasibility of a residential retreat program to address PTSD symptoms in Veterans and First-responders


Clinical Trial Description

After obtaining written consent, participants will complete their program as they had previously intended. Each wave of the residential retreat program will last 5 days. During the program, participants will complete the study questionnaires. They will complete these questionnaires again 1 month after the completion of the program. As a control, individuals completing the program in the online format will also be asked to provide written consent and will complete the questionnaires during the program and 1-month after its completion. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05311696
Study type Observational
Source Valhalla Project Niagara
Contact Pouria Saffaran, Bsc
Phone 647-895-7474
Email pouria.saffaran@alum.utoronto.ca
Status Recruiting
Phase
Start date March 27, 2022
Completion date November 21, 2023

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