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N/A N=15 Treatment

Stimulation of Cingulo-opercular Alertness Network

Lewy Body Disease · Lewy Body Variant of Alzheimer Disease · Lewy Body Dementia With Behavioral Disturbance

Enrolled (actual)
15
Serious AEs
0.0%
Results posted
Oct 2025
Primary outcome: Primary: Dementia Cognitive Fluctuations Scale — 11.75; 8.33 score on a scale — p=<0.001

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
HD-tDCS (Device)
Age
Adult, Older Adult · 50+ yrs
Sex
All
Sponsor
University of Michigan
Primary completion
Aug 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Dementia Cognitive Fluctuations Scale
11.75; 8.33 <0.001 sig
SECONDARY
Resting State fMRI
0.23; 0.33; 0.53; 0.53 0.018 sig
SECONDARY
Stroop Color Word Interference Test - Cognitive Control Performance
143.44; 125.15 0.239
SECONDARY
Objective Measures of Working Memory (N-back Test)
0.94; 1.24 0.168

Summary

Fluctuations in alertness are very common in persons with Lewy body dementias and are a major source of disability. Changes in a chemical messenger molecule called acetylcholine within certain brain regions may play a role in these fluctuations. We propose to test this hypothesis and also determine whether a non-invasive way of stimulating affected brain regions may be of relevance for future management of these fluctuations.

Eligibility Criteria

Inclusion Criteria

  • LBD patients (DLB or PDD) who have cognitive fluctuations and who are on stable doses of cholinesterase inhibitors (i.e., at least 4 weeks) will be recruited to participate in this study.
  • DLB patients will meet the Fourth consensus report of the DLB Consortium inclusion criteria for probable DLB.
  • Subjects will be identified according to the following recognized DLB features: spontaneous parkinsonian motor signs, fluctuating attention and concentration, recurrent well-formed visual hallucinations, presence of REM behavioral sleep disturbance, anosmia/hyposmia,or autonomic dysfunction.
  • PDD patients will meet the criteria by Emre et al. (Cognitive deficits in at least two of four of the following cognitive domains: Impaired attention, impaired executive functions, impairment in visuo-spatial functions, impaired free recall memory typically improved with cuing. Must also meet criteria for at least one behavioral symptom: apathy, depressed or anxious mood, hallucinations, delusions, excessive daytime sleepiness). Lack of behavioral symptoms does not exclude the diagnosis. Must also have none of Group III features present: (1) Co-existence of any other abnormality which might cause impairment, but judged not to be the cause of dementia. (2) Time interval between development of motor and cognitive symptoms not known. Must also have none of Group IV symptoms present: (1) Cognitive and behavioral symptoms appear solely in the context of other conditions such as acute confusion caused by systemic diseases or abnormalities, drug intoxication, or major depression according to DSM IV. (2) Features compatible with Probable Vascular Dementia criteria accordingly to NINDS-AIREN.

Exclusion Criteria

  • Subjects with contra-indications to MR imaging and/or tDCS, including pacemakers or claustrophobia
  • Evidence of large vessel stroke or mass lesion on MRI
  • Use of anti-cholinergic or neuroleptic drugs
  • Evidence of atypical parkinsonism on neurological exam
  • Major psychiatric illness, such as bipolar disorder
  • Neurological conditions such as epilepsy, stroke, multiple sclerosis, or moderate to severe brain injury
  • Sensory impairments that significantly limit one's ability to see or hear
  • A significant history of recent alcohol or drug dependence
  • Previous major radiation exposure
  • Pregnancy
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04817891). 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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