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Treatment for PTSD and Tinnitus
NCT07106593 · The University of Texas Health Science Center at San Antonio
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
Official title
Treatment of TBI-Related Tinnitus and Comorbid PTSD: Examination of Neurobiological Markers Related to Symptom Improvement
About this study
After consenting to this study, study participants will be asked to speak with a study staff member about stressful or traumatic experiences, complete hearing assessments and questionnaires about exposure to traumatic events, PTSD symptoms, mental and physical health problems, such as depression and substance use, head injuries, and tinnitus. Participants who are able and willing may be asked to provide functional magnetic resonance imaging (MRI) scans before and after treatment. Participants will receive treatment for tinnitus and posttraumatic stress disorder (PTSD) in one of two ways: Cognitive Processing Therapy (CPT) first and then Cognitive Behavioral Therapy for Tinnitus (CBT-t) OR CBT-t first, followed by CPT.
Eligibility criteria
Inclusion Criteria:
* Adult male and female active duty military personnel and veterans seeking treatment for PTSD
* Diagnosis of PTSD
* Person has experienced at least one mild traumatic brain injury (concussion)
* Ability to speak and read English
* Stable on any psychotropic medications
* Meets criteria for chronic subjective and bothersome tinnitus
* Chronic tinnitus is at least possibly related to head injury
Exclusion Criteria:
* Currently receiving other talk therapies
* Severe hearing loss that would prevent the participant from benefiting from therapy
* Current severe suicidal ideation
* Psychiatric hospitalization in the last 12 months
* Moderate to severe substance use that would prevent the participant form benefiting from therapy
* Current manic episode or psychotic symptoms requiring immediate stabilization or hospitalization
* Significant cognitive impairment
* Moderate to severe brain damage
* Neurobiological disorders
* Temporomandibular joint disorders and/or Meniere's disease that cause acute pain
Study design
Enrollment target: 160 participants
Allocation: randomized
Masking: single
Age groups: adult, older_adult
Timeline
Starts: 2025-08-08
Estimated completion: 2028-08
Last updated: 2025-08-13
Interventions
Behavioral: Cognitive Processing TherapyBehavioral: CBT-t
Primary outcomes
- • PTSD Checklist (Baseline to 6-Month Follow-Up (approximately12 months))
- • Tinnitus Functional Index (Baseline to 6-Month Follow-Up (approximately12 months))
Sponsor
The University of Texas Health Science Center at San Antonio · other
With: University of Illinois at Urbana-Champaign
Contacts & investigators
ContactAmanda Flores, BA · contact · floresa13@uthscsa.edu · 210-562-6726
InvestigatorJohn Moring, PhD · principal_investigator, The University of Texas Health Science Center at San Antonio
All locations (1)
The University of Texas Health Science Center at San AntonioRecruiting
San Antonio, Texas, United States