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N/A N=31 Randomized Quadruple-blind Treatment

Neuromodulation of Cognition in Older Adults

Healthy

Enrolled (actual)
31
Serious AEs
3.2%
Results posted
May 2023
Primary outcome: Primary: Change in NIH Toolbox Fluid Cognition Composite Score — 4.7; 6.1 units on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Sham Stimulation (Device); Transcranial Direct Current Stimulation (Device)
Age
Older Adult · 65+ yrs
Sex
All
Sponsor
University of Florida
Primary completion
Feb 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in NIH Toolbox Fluid Cognition Composite Score
4.7; 6.1

Summary

This study will investigate whether transcranial direct current stimulation enhances the effects of cognitive training in healthy older adults.

Eligibility Criteria

Inclusion Criteria

  • Men and women
  • Age: 65 to 90 years
  • English speaking
  • Physically mobile
  • working memory function between 0-75th percentile determined by screening results on the POSIT Baseline Cognitive Training computerized tasks.

Exclusion Criteria

  • Neurological disorders (e.g., dementia, stroke, seizures, traumatic brain injury).
  • Evidence of dementia (NACC UDS scores of 1.5 standard deviations below the mean for age, sex and education adjusted norms in a single cognitive domain on the task).
  • Past opportunistic brain infection.
  • Major psychiatric illness (schizophrenia, intractable affective disorder, current substance dependence diagnosis or severe major depression and/or suicidality).
  • Unstable (e.g., cancer other than basal cell skin) and chronic (e.g, severe diabetes) medical conditions.
  • MRI contraindications (e.g., pregnancy, claustrophobia, metal implants that are contraindicated for MRI).
  • Physical impairment precluding motor response or lying still for 1 hr and inability to walk two blocks without stopping.
  • Certain prescription medications may possibly reduce effects otherwise induced by the tDCS stimulation protocol.
  • Hearing or vision deficits that will not allow for standardized cognitive training.
  • Left handedness
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02137122). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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