Methylphenidate for Ptsd and Stroke Veterans

Completed · Phase 1/Phase 2 · Has a placebo group

Conditions studied: PTSD, Stroke

In brief

Veterans with post-traumatic stress disorder (PTSD) have an increased risk of developing ischemic stroke. Veterans enduring PTSD face difficulties in managing their PTSD severity after suffering from a stroke. Currently, clinical trials in PTSD exclude patients with stroke and patients with significant premorbid psychological conditions like PTSD are usually excluded from stroke clinical trials. Methylphenidate (MPH) is a central nervous system stimulant that can improve PTSD symptoms: avoidance behaviors, social withdrawal, hyperarousal, and working memory. MPH can also improve post-stroke outcomes: mood, activities of daily living, and motor functioning. In clinical trials for PTSD or stroke, MPH has been shown to be well-tolerated with minimal adverse events. The high prevalence of PTSD in Veterans with stroke provides strong justification for development of interventions that effectively and simultaneously target both conditions. The overarching goal of our proposal is to understand how MPH improves PTSD severity in Veterans with comorbid stroke.

Key facts

Study ID: NCT04885257
Run by: VA Office of Research and Development
People needed: 20
Starts: 2022-01-14
Expected to finish: 2025-05-05
Last updated by the study team: 2025-06-22

Who can join

Age: 40 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Male or female Veteran of US military; signed informed consent
Criterion A Index Trauma(s) resulting in PTSD occurred during adulthood prior to stroke
CAPS-5 past week total score =23 at baseline visit
Willing to refrain from antipsychotics, mood stabilizers, stimulants, and any formulation of MPH
First-ever symptomatic ischemic stroke radiologically verified, occurring within past 1-12 months
Females of child-bearing potential (i.e. not postmenopausal or surgically sterile) must be using a medically acceptable method of birth control and should not be pregnant nor have plans for pregnancy or breastfeeding during the study

You may not qualify if…

Moderate to severe cognitive impairment (Montreal Cognitive Assessment score <16/30)
Poor pre-stroke baseline function of a modified Rankin score >2
Presence of any standard MRI contraindications
Current diagnosis of DSM-5-defined bipolar disorder I, schizophrenia, schizoaffective disorder, obsessive-compulsive disorder, or major depressive disorder with psychotic features (MINI)
Diagnosis of moderate or severe substance use disorder (except for caffeine and nicotine) during the preceding 3 months
Patients who utilize alcohol or cannabis but do not meet criteria for moderate or severe disorder are permitted at the discretion of the investigator
Participants must agree to abstain from illicit drugs during the study
Increased risk of suicide that necessitates inpatient treatment or warrants additional therapy excluded by the protocol; and/or intensity of suicidal ideation (Type 4 or Type 5) or any suicidal behavior in the past 3 months on Columbia Suicide Severity Rating Scale (C-SSRS)
Use of any investigational drug, MPH formulation, antipsychotics, mood stabilizers, monoamine oxidase inhibitors, stimulants or any medication known to be a potent (strong) cytochrome P450 subtype 3A4 inhibitor within 2 weeks of baseline
Treatment with evidence-based trauma-focused therapy for PTSD within two weeks of baseline (if participant is receiving therapy, he/she must complete treatment prior to entering study)
Supportive psychotherapy in process at time of Screening may be continued during the study.
History of moderate or severe TBI as defined by the Ohio State University TBI Identification Method
Based on investigator's clinical judgment, history of mild TBI is not excluded
Any clinically significant, uncontrolled, or medical/surgical condition or laboratory abnormality that would contraindicate use of MPH (see Human Subjects section)
Severe allergic reaction, bronchospasm, or hypersensitivity to any MPH formulation.
Litigating for compensation for a psychiatric disorder. Veterans who are in the process of applying for or receiving VA service-connected disability are eligible
Current enrollment in another intervention trial for PTSD or stroke
Persons imprisoned, diagnosed with terminal illness, or require surrogate for consent

Where it is running

Birmingham VA Medical Center, Birmingham, AL — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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