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NCT07080606: BEE for PTSD

Brief Exposure and Exercise for PTSD.

Completed NA Last updated 8 April 2026
What this trial tests

NA trial testing Brief exposure therapy and exercise in PTSD - Post Traumatic Stress Disorder in 12 participants. Completed in 2 March 2026.

Timeline
25 June 2025
Primary endpoint
2 March 2026
2 March 2026

Quick facts

Lead sponsorTroy Hubert
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment12
Start date25 June 2025
Primary completion2 March 2026
Estimated completion2 March 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Troy Hubert

Who can join

Adults 18 to 64, any sex, with PTSD - Post Traumatic Stress Disorder. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to learn if 8 sessions of brief exposure and exercise therapy works to treat Post Traumatic Stress Disorder (PTSD) in adults. This study will also learn if participants think brief exposure and exercise therapy is a good and doable treatment. and The main questions it aims to answer are: * Do participants find brief exposure and exercise an acceptable and feasible means of treatment for PTSD? * Does brief exposure and exercise decreases of the severity of PTSD symptoms? Participants will: * Complete weekly questionnaires for 10-14 weeks. * Attend 8 twice weekly exposure therapy and exercise sessions for 4 weeks.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for PTSD - Post Traumatic Stress Disorder

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07080606.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing