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Life sciences · Interventional Study
ClinicalTrials.gov · September 18, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Interventional Study.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
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Registry record from ClinicalTrials.gov (NCT06236711). This is a study registration, not published results. Lead sponsor: Mayo Clinic. Recruitment status: ACTIVE_NOT_RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 10 participants (ESTIMATED). Conditions: Treatment Resistant Depression. Interventions: DEVICE: tDCS. Primary outcome measures: Feasibility outcome , through study completion, an average of 2 weeks; Acceptability outcome , through study completion, an average of 2 weeks; Tolerability outcome , through study completion, an average of 2 weeks. Brief summary: The researchers are trying to test the feasibility and acceptability of using transcranial Direct Current Stimulation (tDCS) in hospitalized adult patients with Treatment Resistant Depression (TRD), assess for any preliminary effect on depressive and cognitive symptoms, and explore the utility of biomarkers to assess response to tDCS.