Skip to content

Predicting Cognition After DBS for Parkinson's Disease 2

Predicting Cognition After DBS for Parkinson's Disease 2

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06272968
Enrollment
30
Registered
2024-02-22
Start date
2024-10-01
Completion date
2030-12-01
Last updated
2026-09-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Impairment

Keywords

Cognitive Impairment, Parkinson's disease, Deep Brain Stimulation, Postoperative Delirium

Brief summary

The aim of the study is to improve estimation of cognitive outcome after STN-DBS in PD in order to avoid risk factors by optimizing peri- and intraoperative management and personalize therapeutic strategies for optimal long-term benefit. The investigators will test possible predictors (clinical, neuropsychological, neuroimaging, electrophysiological and molecular) for the risk of cognitive dysfunction after deep brain stimulation of the subthalamic nucleus (STN-DBS) in Parkinson's disease (PD) at a single center (Charité - Universitätsmedizin Berlin, Germany). Data collection takes place prior to as well as 3, 12 and 60 months after the STN-DBS operation. Participation is proposed to all PD patients that are planned to undergo STN-DBS after careful examination of eligibility for this treatment according to standard operation procedures.

Detailed description

Additionally to clinical routine tests, the following possible predictors of cognitive dysfunction after STN-DBS in PD are investigated: * Imaging biomarkers: volume of the nucleus basalis of Meynert (NBM) measured on preoperative MRI and data driven search for unknown MRI characteristics relating to the incidence of postoperative neurocognitive disorder by means of Deep Learning (Convolutional Neural Networks), test of previously established classification models * Imaging neuronal glucose metabolism with \[18F\]-DG PET * Comorbidity: according to the Charlson Comorbidity Index * Nutritional Status: defined by the Mini Nutritional Assessment (MNA-SF) * Functional assessment of neuronal activity by 64-channel-EEG * Duration of intra-/perioperative brake of dopaminergic medication * Nature and depth of anaesthesia: general or conscious sedation and depth of consciousness: as measured by 4 channel electroencephalography (SedLine®) and during implantation of impulse generator * Incidence and duration of postoperative delirium: defined according to the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) and/or as ≥ 2 points in the nursing Delirium Screening Scale (Nu-DESC) and/or a positive Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) score, assessment three times daily during hospital stay * Length of stay at ICU / hospital * Postoperative organ complications: according to Clavien-Dindo classification Localisation of bilateral electrodes and active contacts on postoperative imaging Substudies Correlation of domain specific CANTAB connect test scores with possible predictors and incidence of postoperative neurocognitive disorder with CANTAB assessments performed with STN-DBS stimulation switched on and off at 12- and 60-month follow-up. The resulting multivariate risk model is expected * to improve peri- and intraoperative management by identifying avoidable risk factors for the development of postoperative cognitive deficit * to support evidence-based and personalized decision-making when advising PD patients considering STN-DBS * to result in the development of future hypothesis-driven interventional trials on the basis of biomarker-based sub-grouping of patients * to allow a better understanding of underlying pathophysiological processes both PD and surgery-related regarding cognitive effects of STN-DBS.

Interventions

DIAGNOSTIC_TESTNeuropsychological Testing

Neuropsychological Testing via Cambridge CANTAB Connect

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of idiopathic Parkinson's Disease * Indication for STN-DBS

Exclusion criteria

* Internistic, surgical or psychiatric contrainidications with respect to the DBS operation or treatment for the STN-DBS group * Dementia * Relevant language barrier

Design outcomes

Primary

MeasureTime frameDescription
Change in cognitive performance after STN-DBSDifference between baseline, 12 and 60 months postoperative testingBased on cognitive screening by Cambridge CANTAB Connect
Incidence of postoperative neurocognitive disorderDifference between baseline, 12 and 60 months postoperative testingBased on cognitive screening by paper pencil test (MoCA or MDRS)

Secondary

MeasureTime frameDescription
Validation of post-hoc model from prior study (NCT03982953)1 year after DBS surgeryMoCA1yFU = 0.7 × MoCAbaseline + 1.7 × backward spanbaseline - 1, (see https://doi.org/10.1038/s41531-025-01128-3)

Countries

Germany

Contacts

STUDY_CHAIRDorothee Kübler-Weller, MD

Movement Disorders and Neuromodulation

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 4, 2026