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Residential Retreat for Veterans and First-responders

V

Valhalla Project Niagara

Status

Unknown

Conditions

PTSD

Treatments

Other: psychoeducation

Study type

Observational

Funder types

Industry

Identifiers

Details and patient eligibility

About

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

Full 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.

Enrollment

70 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of PTSD, being a military veteran or first-responder, awareness of treating physician about program attendance

Exclusion criteria

  • None

Trial design

70 participants in 2 patient groups

Residential Cohort
Description:
Those completing the program in a residential context
Treatment:
Other: psychoeducation
Online Cohort
Description:
Those completing the program online
Treatment:
Other: psychoeducation

Trial contacts and locations

1

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Central trial contact

Pouria Saffaran, Bsc

Data sourced from clinicaltrials.gov

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