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Recruiting NCT06300255

Evaluation of the H.O.O.V.E.S. Healing Intensives Program

Observational Anxiety PTSD Depression

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: H.O.O.V.E.S. Healing Intensives.
Who it may be relevant to
Registry conditions: Anxiety, PTSD, Depression. Basic parameters: 18 years — 120 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The aim of this study is to measure the impact of these H.O.O.V.E.S. healing intensives on Veteran participants using several psychological instruments. The investigators are planning to administer the demographic questionnaires and psychological instruments to Veteran participants before the healing intensives. Psychological instruments will be administered immediately pre-intervention, pre- and post-session for each session, post-intervention, 90, 120 and 360 days post-intervention. The primary aim is to assess for statistically significant changes pre- to post session and pre- to post-intervention.

Interventions

  • Behavioral H.O.O.V.E.S. Healing Intensives
    "H.O.O.V.E.S. is a private, donor-supported charity dedicated to providing fully-funded, \[4\]-day, non-clinical healing intensives for veterans, their families and caregivers, and first responders across the nation who are seeking recovery from service-connected stress." 1 References 1\. Home. HOOVES for Vets. Accessed January 24, 2024. https://www.hooves.us/.

Primary outcome measures

  • Mean Difference in AAQII pre- to post-session and pre- to post-intervention [Time frame: through study completion, an average of 5 years]
  • Mean Difference in PANAS pre- to post-session and pre- to post-intervention [Time frame: through study completion, an average of 5 years]
  • Mean Difference in STAI pre- to post-session and pre- to post-intervention [Time frame: through study completion, an average of 5 years]
  • Mean Difference in PCL pre- to post-session and pre- to post-intervention [Time frame: through study completion, an average of 5 years]
  • Mean Difference in BDI pre- to post-session and pre- to post-intervention [Time frame: through study completion, an average of 5 years]
  • Mean Difference in PTGI pre- to post-session and pre- to post-intervention [Time frame: through study completion, an average of 5 years]
  • Mean Difference in B-SCS pre- to post-session and pre- to post-intervention [Time frame: through study completion, an average of 5 years]
Secondary outcome measures (3)
  • Mean Difference in AAQII pre- to post-session [Time frame: through study completion, an average of 5 years]
  • Mean Difference in PANAS pre- to post-session [Time frame: through study completion, an average of 5 years]
  • Mean Difference in STAI pre- to post-session [Time frame: through study completion, an average of 5 years]

Eligibility criteria

Inclusion criteria

  • Veterans who have served in the military
  • Must be enrolled in a H.O.O.V.E.S. Healing Intensives Program
  • English speakers

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • George E. Wahlen Department of Veterans Affairs Medical Center — Salt Lake City

Identifiers

NCT: NCT06300255 · IRB 00166616

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗