Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT05843695 · ClinicalTrials.gov registry record · NA
Enhancing Psychotherapy for Veterans and Service Members With PTSD and Anxiety
A NA study of Post Traumatic Stress Disorder and Anxiety Disorders, sponsored by Baylor College of Medicine.
- Recruiting
- Registry status
- NA
- Development phase
- 306
- Enrollment target
- 1
- Study location
NCT05843695: Recruiting NA study of Post Traumatic Stress Disorder and Anxiety Disorders, sponsored by Baylor College of Medicine.
NCT05843695 is a NA study of Post Traumatic Stress Disorder and Anxiety Disorders that is actively recruiting participants, run by Baylor College of Medicine. The registered enrollment target is 306 participants, below the 663-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (54% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05843695, a NA study of Post Traumatic Stress Disorder and Anxiety Disorders, is actively recruiting participants, sponsored by Baylor College of Medicine.
- RECRUITING
- Registry status
- NA
- Development phase
- 306 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to compare two different intensive formats of delivering cognitive-behavioral treatment for people with PTSD and anxiety disorders. The main questions it aims to answer are: * Is iTCBT delivered in individual and group formats more effective than TAU in improving anxiety symptoms and quality of life? * For treatment non-responders, is iTCBT-Enhanced more effective than TAU improving anxiety symptoms and quality of life? * Does iTCBT-Individual produce a larger improvement in anxiety and quality of life compared with iTCBT-Group? Participants will undergo several assessments throughout the course of the study. Based on randomization, they will receive: (1) iTCBT in an individual format over a 2-week period, (2) iTCBT in a group format over a 2-day period, or (3) usual care. Those who do not show a response to treatment will receive 4 additional individual therapy sessions.
Primary Outcome
The QLES-Q-SF measures subjective functioning and satisfaction across a range of life domains including work, leisure activities, social relationships, and physical health. Satisfaction scores on this measure range from 14 (very poor) to 70 (very good). Higher scores indicate greater overall life satisfaction and functioning.
Conditions Studied
Interventions
- BEHAVIORAL TAU
- BEHAVIORAL iTCBT-I
- BEHAVIORAL iTCBT-G
Study Locations (1)
Texas
- Michael E. DeBakey VA Medical Center - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 306 participants |
| Start Date | 2023-09-22 |
| Est. Completion | 2027-03-30 |
| Phase | NA |
What NCT05843695 shows while recruiting
NCT05843695 is an interventional study that assigns participants to a tested intervention. The registered 306 participants enrollment target is mid-sized for trials with a published cap, below the 663-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (54% lower).
The record links to 2 conditions, with Post Traumatic Stress Disorder appearing as the primary indexed condition, and to 3 interventions - of which TAU is the first listed.
NCT05843695 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT05843695 about?
NCT05843695 is a clinical study titled "Enhancing Psychotherapy for Veterans and Service Members With PTSD and Anxiety". The goal of this clinical trial is to compare two different intensive formats of delivering cognitive-behavioral treatment for people with PTSD and anxiety disorders. The main questions it aims to answer are: * Is iTCBT delivered in individual and group formats more effective than TAU in improving ...
What is the current status of trial NCT05843695?
This trial is currently recruiting. It is a NA study. The enrollment target is 306 participants. The study started on 2023-09-22. Estimated completion is 2027-03-30.
What conditions does trial NCT05843695 study?
This clinical trial studies the following conditions: Post Traumatic Stress Disorder, Anxiety Disorders.
What interventions are being tested in trial NCT05843695?
The interventions under investigation include: TAU (BEHAVIORAL), iTCBT-I (BEHAVIORAL), iTCBT-G (BEHAVIORAL).
Who is sponsoring clinical trial NCT05843695?
This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05843695 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Post Traumatic Stress Disorder
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT05843695's enrollment target sits among peer trials
306 25th of 262 higher than 238 of 262 other Post Traumatic Stress Disorder trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Post Traumatic Stress Disorder trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
Exploring Virtual Reality Adventure Training Exergaming
RECRUITING · NA
-
CRISOL Mente: A Multilevel Community Intervention to Reduce Mental Health Disparities Among Latinos
RECRUITING · NA
-
TMS-fNIRS Personalized Dosing
RECRUITING · NA
-
Targeting the Default Mode Network: A TMS-fMRI Study
RECRUITING · NA
-
The Effects of Very Brief Exposure on PTSD in U.S. Combat Veterans
RECRUITING · NA
-
Fear and Avoidance in PTSD Patients
RECRUITING · NA
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT05078970 · 306 participants · NA
Advancing Suicide Intervention Strategies for Teens During High Risk Periods
- NCT06057337 · 306 participants · NA
Families With Pride ("Familias Con Orgullo").
- NCT06498635 · 306 participants · Phase 3
Immunotherapy After Surgery for People Who Have No Remaining Cancer Cells After Standard Treatment for Early-Stage Non-Small Cell Lung Cancer, INSIGHT Trial
- NCT06534918 · 306 participants · NA
Precise Oncology Interventions in Nutrition and Training (OnPoint)
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI