Life sciences · Interventional Study
ClinicalTrials.gov · October 2, 2026
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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 (NCT05400512). This is a study registration, not published results. Lead sponsor: Vanderbilt University Medical Center. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 16 participants (ACTUAL). Conditions: Aging, Depression, Cognitive Symptom. Interventions: BEHAVIORAL: Cognitive Training; DEVICE: tDCS (active stimulation); DEVICE: tDCS (sham stimulation). Primary outcome measures: Task-based fMRI Activation Within the Cognitive Control Network During the N-back Task , From baseline (T1) to post-intervention (4-6 weeks; T2); N-back Behavioral Performance (Accuracy) , From baseline (T1) to post-intervention (4-6 weeks; T2); N-back Behavioral Performance (Response Time) , From baseline (T1) to post-intervention (4-6 weeks; T2); NIH Examiner Scores , From baseline (T1) to post-intervention (4-6 weeks; T2). Brief summary: This study will investigate whether transcranial direct current stimulation (tDCS) enhances the effects of computerized cognitive training in older adults with recurrent depression (2 or more lifetime episodes; either current or within past 3 years).