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Residential Retreat for Veterans and First-responders

Examining the Efficacy and Feasibility of a Residential Retreat Program for PTSD in First-responders and Veterans: A Non-randomized Controlled Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05311696
Enrollment
70
Registered
2022-04-05
Start date
2022-03-27
Completion date
2023-11-21
Last updated
2022-04-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

PTSD

Brief 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

Detailed 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.

Interventions

OTHERpsychoeducation

The program consists of psychoeducational material regarding PTSD, demonstration of various stress management techniques, and social cohesion activities

Sponsors

Valhalla Project Niagara
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Symptom Management of PTSD Using the Perceived Medical Condition Self-Management Scale1-month after completion of the programdetermining the potential efficacy of the residential program for improving symptom management. The scale is adapted to reflect participants management of their PTSD symptoms. Score ranges from 8 to 40. Higher scores indicate better management.
Drop-out rate in the Residential Programat the end of the 5-day residential program for the residential cohortDetermining the extent of treatment drop-out in the Residential Program
Symptoms of PTSD Indicated by the PTSD Checklist for DSM-5 scale.1-month after completion of the programdetermining the potential efficacy of the residential program for improving PTSD symptoms. Scores range from 0 to 80. Higher scores indicate more symptoms of PTSD.
Interpersonal and Intrapersonal Functioning Using the Brief Inventory of Psychosocial Functioning (B-IPF)1-month after the completion of the programdetermining the potential efficacy of the residential program for improving interpersonal and intrapersonal functioning (e.g., relationship with family, ability to manage daily tasks, etc.). Scores range from 0 to 42. Higher scores indicate more problems and lower functioning.
Drop-out rate in the Online Programat the end of the 2 month online program for the online cohort.Determining the extent of treatment drop-out in the Online Program

Countries

Canada

Contacts

Primary ContactPouria Saffaran, Bsc
pouria.saffaran@alum.utoronto.ca647-895-7474

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026