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        <identifier>oai:figshare.com:article/33981433</identifier>
        <datestamp>2026-09-24T10:40:18Z</datestamp>
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          <dc:title>Supplementary file 1_Effect of transcranial alternating current stimulation (NET Device™) on psychostimulant withdrawal severity and time course: a real-world data analysis.docx</dc:title>
          <dc:creator>Mark K. Greenwald (6897305)</dc:creator>
          <dc:creator>Lana R. Grasser (25103488)</dc:creator>
          <dc:creator>Joe R. Winston (20749253)</dc:creator>
          <dc:subject>Psychiatry (incl. Psychotherapy)</dc:subject>
          <dc:subject>ACSA</dc:subject>
          <dc:subject>NET device</dc:subject>
          <dc:subject>neuromodulation</dc:subject>
          <dc:subject>psychostimulant withdrawal</dc:subject>
          <dc:subject>real-world data</dc:subject>
          <dc:subject>real-world evidence</dc:subject>
          <dc:subject>stimulant use disorder</dc:subject>
          <dc:subject>transcranial alternating current stimulation</dc:subject>
          <dc:description>Background&lt;p&gt;Psychostimulant use disorder is a life-threatening condition with no FDA-approved treatment. Stimulant withdrawal symptoms impede treatment engagement and are unaddressed by standard of care. The NET Device, a non-invasive transcranial alternating current stimulator, is FDA-cleared for opioid withdrawal suppression. No studies have evaluated whether NET Device use attenuates psychostimulant withdrawal.&lt;/p&gt;Methods&lt;p&gt;Electronic health record and device utilization data were collected from 109 stimulant-only users and 112 stimulant/opioid co-users (N = 221 adults total; M&lt;sub&gt;age&lt;/sub&gt;=39.2, SD&lt;sub&gt;age&lt;/sub&gt;=10.7; 119M) entering residential addiction treatment (n = 168) or detention centers (n = 53). The Amphetamine Cessation Symptom Assessment (ACSA) was administered at baseline and 1 hour (day 1), and twice daily on days 1–7. A linear mixed model (LMM) with random intercepts and slopes was used to analyze the trajectory of ACSA scores.&lt;/p&gt;Results&lt;p&gt;ACSA severity and time course were similar across settings (residential vs. detention). A two-phase LMM separated acute (baseline to 1 hour) and post-acute withdrawal symptom reductions. Relative to baseline ACSA scores, stimulant-only and co-user groups each reported significant reductions at 1 hour (46% and 33%), day 2 morning (59% and 42%), and decelerating log-time trajectory through day 4 (79 hours), the primary analysis window. Estimates beyond day 4 rest on 6.9% of observations and are reported as exploratory only.&lt;/p&gt;Conclusion&lt;p&gt;NET Device monotherapy was associated with rapid reduction in psychostimulant withdrawal severity regardless of setting and opioid co-use. No device-related adverse events were reported. These real-world data support initiation of a sham-controlled randomized trial to evaluate NET Device efficacy for stimulant use disorder.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-24T10:40:18Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fpsyt.2026.1899599.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Supplementary_file_1_Effect_of_transcranial_alternating_current_stimulation_NET_Device_on_psychostimulant_withdrawal_severity_and_time_course_a_real-world_data_analysis_docx/33981433</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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