Methylphenidate for Ptsd and Stroke Veterans

Stroke Clinical Trial

Official title:

A Randomized Placebo-controlled Trial of Methylphenidate in Veterans With a Diagnosis of Post Traumatic Stress Disorder and Recent Cerebral Stroke.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04885257
• Other study ID #: MHBP-011-20F
• Secondary ID: IK2CX002104
• Status: Recruiting
• Phase: Phase 2
• Start date: January 14, 2022
• Est. completion date: September 30, 2026

Study information

• Verified date: December 2023
• Source: VA Office of Research and Development
• Contact: Chen Lin, MD
• Phone: (205) 933-8101
• Email: Chen.Lin[@]va.gov
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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 blocks dopamine and norepinephrine transporters, selectively increasing prefrontal cortex (PFC) activity. MPH can improve PTSD symptoms: avoidance behaviors, social withdrawal, hyperarousal, and working memory. The suspected mechanism is MPH activates PFC, enhancing fear extinction and improving PTSD symptoms. 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. The purpose of the clinical trial is to evaluate the therapeutic effects on PTSD symptoms and post-stroke recovery of placebo-controlled MPH in Veterans diagnosed with PTSD and cerebral stroke.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: September 30, 2026
• Est. primary completion date: September 30, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Male or female Veteran of US military; signed informed consent

• Criterion A Index Trauma(s) resulting in PTSD occurred during adulthood prior to stroke

• PTSD defined by MINI International Neuropsychiatric Inventory (MINI) for DSM-5

• CAPS-5 past week total score =27 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

Exclusion Criteria:

• 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

Related Conditions & MeSH terms

• PTSD
• Stroke

Intervention

Drug:
• Methylphenidate
Methylphenidate oral pill. Dosing instructions given to
• Placebo
Placebo arm

Locations

Country	Name	City	State
United States	Birmingham VA Medical Center, Birmingham, AL	Birmingham	Alabama

Sponsors (1)

Lead Sponsor	Collaborator
VA Office of Research and Development

Country where clinical trial is conducted

United States, 

References & Publications (2)

Grade C, Redford B, Chrostowski J, Toussaint L, Blackwell B. Methylphenidate in early poststroke recovery: a double-blind, placebo-controlled study. Arch Phys Med Rehabil. 1998 Sep;79(9):1047-50. doi: 10.1016/s0003-9993(98)90169-1. — View Citation

McAllister TW, Zafonte R, Jain S, Flashman LA, George MS, Grant GA, He F, Lohr JB, Andaluz N, Summerall L, Paulus MP, Raman R, Stein MB. Randomized Placebo-Controlled Trial of Methylphenidate or Galantamine for Persistent Emotional and Cognitive Symptoms — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinician-Administered Post-traumatic stress disorder scale	Structured measure used to confirm the threshold for PTSD symptoms and assess symptom severity. Total symptom severity score is calculated by summing severity scores for 20 PTSD symptoms. Each symptom can score between 0-4, with a range from 0 to 80. Higher scores indicate more severe symptoms.	through study completion, an average of 6 months
Secondary	Modified Rankin Scale	single-item global Likert-type scale ranging from 0-6 (higher scores mean a worse outcome) to categorize level of functional independence with comparison to pre-stroke function, accounting for activities of daily living.	through study completion, an average of 6 months