Dose-finding Study of Selective Serotonin Reuptake Inhibitors to Enhance Neuroplasticity
Trial Snapshot
- Phase
- Phase 1
- Status
- Withdrawn
- Sponsor
- Locations
- 1
- Primary Endpoint
- Change in motor evoked potential amplitude
Study Overview
Brief Summary
The brain is able to change throughout life in response to learning, or injury, or to adapt to changes in the environment, which is known as neuroplasticity. Stroke survivors suffer disabling chronic motor impairments that have proven challenging to improve. Increasing neuroplasticity using selective serotonin reuptake inhibitors (SSRIs) is a promising approach to promote motor recovery in patients with stroke.
Detailed Description
The brain is able to change throughout life in response to learning, or injury, or to adapt to changes in the environment, which is known as neuroplasticity. Stroke survivors suffer disabling chronic motor impairments that have proven challenging to improve. Increasing neuroplasticity using selective serotonin reuptake inhibitors (SSRIs) is a promising approach to promote motor recovery in patients with stroke. Selective serotonin reuptake inhibitors (SSRIs) are currently widely used for treatment of depression, but they also have been shown to be able to enhance neuroplasticity. A single dose of SSRI has been shown to improve hand function in patients with chronic stroke. SSRIs also enhance neuroplasticity in healthy individuals, as shown using paired associative stimulation (PAS), a non-invasive method which causes the brain's excitability to change. However, the best dose of SSRI to increase neuroplasticity is not yet established.
The purpose of this study is to (1) find the effective dose of the SSRI escitalopram to modulate PAS-induced plasticity in patients with stroke and healthy individuals and (2) determine the variability of escitalopram's effect on PAS-induced plasticity between individuals. We measure neuroplasticity with PAS, which causes the brain's excitability to change. During PAS, you would receive electrical stimulation over your wrist and magnetic stimulation to their scalp (called transcranial magnetic stimulation, or TMS) to increase the excitability of the motor area of the brain. You will be asked to participate in a screening visit and 8 study visits separated by at least 1 week. At each study visit, you will be given a single dose of escitalopram (5, 10 or 20) or placebo, and we will measure your brain's change in excitability after PAS.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Crossover
- Primary Purpose
- Treatment
- Masking
- Triple (Participant, Investigator, Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Arms & Interventions
Administration of SSRI
Participants will be administered either 5, 10 or 20mg of SSRI escitalopram prior to paired associative stimulation.
Intervention: Administration of SSRI escitalopram (Drug)
Administration of SSRI
Participants will be administered either 5, 10 or 20mg of SSRI escitalopram prior to paired associative stimulation.
Intervention: Paired Associative stimulation (Behavioral)
Administration of Placebo
Participants will be administered a placebo prior to paired associative stimulation
Intervention: Paired Associative stimulation (Behavioral)
Administration of Placebo
Participants will be administered a placebo prior to paired associative stimulation
Intervention: Administration of Placebo (Drug)
Outcomes
Primary Outcomes
Change in motor evoked potential amplitude
Time Frame: Baseline, Up to 30 minutes Post PAS
Assessment of corticospinal excitability
Secondary Outcomes
No secondary outcomes reported
Investigators
Tomoko Kitago
Lab Director Human Motor Recovery Laboratory Assistant Professor
Burke Medical Research Institute
