Residential Retreat for Veterans and First-responders

Sponsor
Valhalla Project Niagara (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05311696
Collaborator
(none)
70
1
19.8
3.5

Study Details

Study Description

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

Condition or Disease Intervention/Treatment Phase
  • Other: psychoeducation

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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
70 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Examining the Efficacy and Feasibility of a Residential Retreat Program for PTSD in First-responders and Veterans: A Non-randomized Controlled Study
Anticipated Study Start Date :
Mar 27, 2022
Anticipated Primary Completion Date :
Nov 21, 2022
Anticipated Study Completion Date :
Nov 21, 2023

Arms and Interventions

Arm Intervention/Treatment
Residential Cohort

Those completing the program in a residential context

Other: psychoeducation
The program consists of psychoeducational material regarding PTSD, demonstration of various stress management techniques, and social cohesion activities
Other Names:
  • demonstration of stress management techniques
  • social cohesion activities
  • Online Cohort

    Those completing the program online

    Other: psychoeducation
    The program consists of psychoeducational material regarding PTSD, demonstration of various stress management techniques, and social cohesion activities
    Other Names:
  • demonstration of stress management techniques
  • social cohesion activities
  • Outcome Measures

    Primary Outcome Measures

    1. Symptom Management of PTSD Using the Perceived Medical Condition Self-Management Scale [1-month after completion of the program]

      determining 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.

    2. Drop-out rate in the Residential Program [at the end of the 5-day residential program for the residential cohort]

      Determining the extent of treatment drop-out in the Residential Program

    3. Symptoms of PTSD Indicated by the PTSD Checklist for DSM-5 scale. [1-month after completion of the program]

      determining the potential efficacy of the residential program for improving PTSD symptoms. Scores range from 0 to 80. Higher scores indicate more symptoms of PTSD.

    4. Interpersonal and Intrapersonal Functioning Using the Brief Inventory of Psychosocial Functioning (B-IPF) [1-month after the completion of the program]

      determining 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.

    5. Drop-out rate in the Online Program [at the end of the 2 month online program for the online cohort.]

      Determining the extent of treatment drop-out in the Online Program

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts 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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Valhalla Project Niagara Niagara-on-the-lake Ontario Canada L0S 1J0

    Sponsors and Collaborators

    • Valhalla Project Niagara

    Investigators

    • Principal Investigator: Jaan Reitav, PhD, C.Psych, Canadian Memorial Chiropractic College

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Valhalla Project Niagara
    ClinicalTrials.gov Identifier:
    NCT05311696
    Other Study ID Numbers:
    • 2650
    First Posted:
    Apr 5, 2022
    Last Update Posted:
    Apr 5, 2022
    Last Verified:
    Mar 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Apr 5, 2022