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NCT06094933: MARI

Mobile Anger Reduction Intervention

Recruiting now NA Last updated 20 October 2025
What this trial tests

NA trial testing Mobile Anger Reduction Intervention (MARI) in Posttraumatic Stress Disorder in 150 participants. Currently enrolling.

Timeline
12 November 2024
Primary endpoint
30 October 2027
31 March 2028

Quick facts

Lead sponsorVA Office of Research and Development
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment150
Start date12 November 2024
Primary completion30 October 2027
Estimated completion31 March 2028
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

VA Office of Research and Development — full company profile →

Who can join

Eligibility, any sex, with Posttraumatic Stress Disorder or Anger. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Difficulty controlling anger is the most commonly reported reintegration concern among combat Veterans, especially those with a diagnosis of posttraumatic stress disorder (PTSD). Problematic anger is associated with significant functional impairment. In the current project, the investigators will compare the Mobile Anger Reduction Intervention (MARI) with a health education mobile intervention (HED) among Veterans with PTSD and problematic anger. Participants will be randomized to the MARI or HED condition. The hypothesis is that participants in the MARI condition will experience greater anger reductions and functional improvements relative to the HED condition.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Posttraumatic Stress Disorder

Currently open trials in the same condition.

Other VA Office of Research and Development trials

Trials by the same sponsor.

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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/NCT06094933.

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