Clinical Trials Directory

Trials / Completed

CompletedNCT06335589

Adapting Treatment Delivery to Improve Retention in Evidence-Based PTSD Treatment

Adapting Treatment Delivery to Improve Retention in Evidence-Based PTSD Treatment (CDA 21-191)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
VA Office of Research and Development · Federal
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Posttraumatic stress disorder (PTSD) is prevalent among Veterans and effective evidence-based psychotherapies (EBPs) for PTSD have been implemented within the Veterans Health Administration (VHA). However, retention in PTSD EBPs is poor. Premature dropout is associated with worse clinical outcomes and greater healthcare utilization. Delivery of PTSD EBPs in a massed format, typically three or more days per week delivered within a month, have shown promise for increasing retention. The present study is a pilot feasibility and acceptability study comparing massed PTSD treatment to treatment as usual (e.g., typically weekly treatment).

Conditions

Interventions

TypeNameDescription
OTHEREBP-MassedCPT or PE will be delivered in a massed format (e.g., sessions at least 3 days per week)
OTHEREBP-TAUCPT or PE will be delivered treatment as usual, which is typically once per week.

Timeline

Start date
2024-06-24
Primary completion
2025-09-15
Completion
2025-09-15
First posted
2024-03-28
Last updated
2026-01-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06335589. Inclusion in this directory is not an endorsement.