Deep Brain Stimulation for Patients With Dementia With Lewy Bodies
Primary Purpose
Dementia With Lewy Bodies
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Bilateral Nucleus Basalis Meynert DBS
Sham Nucleus Basalis Meynert DBS
Sponsored by
About this trial
This is an interventional treatment trial for Dementia With Lewy Bodies
Eligibility Criteria
Inclusion Criteria:
- DLB Consortium Criteria for diagnosis
- Score between 2 & 12 on Clinician Assessment of Fluctuations scale
- MMSE score between 21 and 27
- Appropriate Surgical candidates in terms of general health
- Aged between 50 & 80
- Able to give Informed consent
- Living at home with Carer
- Able to comply with protocol
- On stable dosage of cholinesterase inhibitor
Exclusion Criteria:
- Diagnosis of other cause for dementia
- Abnormality on brain imaging considered likely to compromise compliance with trial protocol.
- Prior intracerebral surgical intervention
Sites / Locations
- UCL Institute of Neurology
- University of Newcastle
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Sham Comparator
Arm Label
Bilateral Nucleus Basalis Meynert DBS
Sham Nucleus Basalis Meynert DBS
Arm Description
6 week period of active NBM DBS
6 week period of Sham DBS
Outcomes
Primary Outcome Measures
Hopkins Verbal Learning test
Verbal Fluency
Simple & Choice Reaction time task
Wechsler Adult Intelligence scale (WAIS IV) Digit Span
Posner's Covert Attention test
Clinician's Assessment of Fluctuations scale
Secondary Outcome Measures
Minimental State Examination (MMSE)
Dementia Rating Scale (DRS-2)
Wechsler Abbreviated Scale of Intelligence (WASI)
Short Recognition Memory
Wechsler Adult Intelligence Scale IV -Letter, Number sequencing
Trail Making test
Stroop test
Wechsler Adult Intelligence Scale IV - Symbol search
Judgement of Line Orientation
North East Visual Hallucinations Interview
Neuropsychiatric Inventory
Florida Apraxia Screening test
Clinical Global Impression Scale
Hamilton Depression scale
Hamilton Anxiety Scale
Starkstein Apathy Rating scale
Movement Disorders Society- Unified Parkinson's Disease Rating Scale
Freezing of Gait- questionnaire
Scales for outcome in Parkinson's disease (SCOPA - AUT)
Quality of Life- Alzheimer's Disease
Mayo Fluctuations Composite Scale
Blessed Dementia scale
Carer Strain Index
Short Form 36
Full Information
NCT ID
NCT02263937
First Posted
September 30, 2014
Last Updated
October 28, 2016
Sponsor
University College, London
1. Study Identification
Unique Protocol Identification Number
NCT02263937
Brief Title
Deep Brain Stimulation for Patients With Dementia With Lewy Bodies
Official Title
Double Blind, Randomised, Dual Centre, Crossover, Pilot Trial of Bilateral Nucleus Basalis of Meynert Deep Brain Stimulation to Improve Cognitive Deficits in Patients With Dementia With Lewy Bodies.
Study Type
Interventional
2. Study Status
Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
January 2014 (undefined)
Primary Completion Date
October 2016 (Actual)
Study Completion Date
October 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University College, London
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This trial aims to collect pilot data to explore whether bilateral deep brain stimulation (DBS) of the Nucleus Basalis of Meynert (NBM) has beneficial effects on memory and thinking impairments among individuals with Dementia with Lewy Bodies (DLB).
Detailed Description
We will perform a pilot study to evaluate the effectiveness of human NBM DBS at improving cognitive deficits in DLB patients. Six patients with DLB with moderate cognitive impairments (including but not restricted to deficits in attention and working memory) will have bilateral DBS electrodes implanted to ensure that superficial contacts lie in the motor Globus Pallidum interna (GPi) target, while the deepest electrical contacts lie in the NBM. We will place electrodes using our conventional image-guided, stereotactic frame-based procedure. Once the surgical wounds have healed, patients will be randomised into 2 groups in a crossover trial design to have 6 week periods of NBM stimulation switched on or switched off separated by a 2 week washout period, following which the patient will cross over to have the opposite condition for a further 6 weeks. Outcome measures collected at the 6 weeks and 14 weeks timepoints will be compared according to whether each patient was ON or OFF stimulation at that timepoint.
At the end of the crossover period, all patients will be invited for continued follow up with stimulation switched on and will have neuropsychological evaluations at 6 monthly intervals. Patients will be given the option of receiving additional conventional stimulation to the motor GPi, through the higher contacts of each electrode, at the end of the crossover period if required for any coexisting Parkinsonian motor complications of DLB.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dementia With Lewy Bodies
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
6 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Bilateral Nucleus Basalis Meynert DBS
Arm Type
Active Comparator
Arm Description
6 week period of active NBM DBS
Arm Title
Sham Nucleus Basalis Meynert DBS
Arm Type
Sham Comparator
Arm Description
6 week period of Sham DBS
Intervention Type
Procedure
Intervention Name(s)
Bilateral Nucleus Basalis Meynert DBS
Other Intervention Name(s)
Active Deep Brain Stimulation
Intervention Description
Low frequency stimulation applied using standard Deep brain stimualtion hardware.
Intervention Type
Procedure
Intervention Name(s)
Sham Nucleus Basalis Meynert DBS
Other Intervention Name(s)
Sham DBS
Intervention Description
DBS system switched off.
Primary Outcome Measure Information:
Title
Hopkins Verbal Learning test
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Verbal Fluency
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Simple & Choice Reaction time task
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Wechsler Adult Intelligence scale (WAIS IV) Digit Span
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Posner's Covert Attention test
Time Frame
Comparing ON v OFF at 6 weeks & 14 weeks according to stimulation status
Title
Clinician's Assessment of Fluctuations scale
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Secondary Outcome Measure Information:
Title
Minimental State Examination (MMSE)
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Dementia Rating Scale (DRS-2)
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Wechsler Abbreviated Scale of Intelligence (WASI)
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Short Recognition Memory
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Wechsler Adult Intelligence Scale IV -Letter, Number sequencing
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Trail Making test
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Stroop test
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Wechsler Adult Intelligence Scale IV - Symbol search
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Judgement of Line Orientation
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
North East Visual Hallucinations Interview
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Neuropsychiatric Inventory
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Florida Apraxia Screening test
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Clinical Global Impression Scale
Time Frame
Comparing ON v OFF at 6 weeks & 14 weeks according to stimulation status
Title
Hamilton Depression scale
Time Frame
Comparing ON v OFF at 6 weeks & 14 weeks according to stimulation status
Title
Hamilton Anxiety Scale
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Starkstein Apathy Rating scale
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Movement Disorders Society- Unified Parkinson's Disease Rating Scale
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Freezing of Gait- questionnaire
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Scales for outcome in Parkinson's disease (SCOPA - AUT)
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Quality of Life- Alzheimer's Disease
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Mayo Fluctuations Composite Scale
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Blessed Dementia scale
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Carer Strain Index
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Title
Short Form 36
Time Frame
Comparing ON v OFF stimulation at 6 weeks & 14 weeks according to stimulation status
Other Pre-specified Outcome Measures:
Title
Adverse Events
Time Frame
Throughout trial period
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
DLB Consortium Criteria for diagnosis
Score between 2 & 12 on Clinician Assessment of Fluctuations scale
MMSE score between 21 and 27
Appropriate Surgical candidates in terms of general health
Aged between 50 & 80
Able to give Informed consent
Living at home with Carer
Able to comply with protocol
On stable dosage of cholinesterase inhibitor
Exclusion Criteria:
Diagnosis of other cause for dementia
Abnormality on brain imaging considered likely to compromise compliance with trial protocol.
Prior intracerebral surgical intervention
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas Foltynie, MB BS MRCP
Organizational Affiliation
UCL Institute of Neurology
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCL Institute of Neurology
City
London
ZIP/Postal Code
WC1N 3BG
Country
United Kingdom
Facility Name
University of Newcastle
City
Newcastle
Country
United Kingdom
12. IPD Sharing Statement
Citations:
PubMed Identifier
32334074
Citation
Gratwicke J, Zrinzo L, Kahan J, Peters A, Brechany U, McNichol A, Beigi M, Akram H, Hyam J, Oswal A, Day B, Mancini L, Thornton J, Yousry T, Crutch SJ, Taylor JP, McKeith I, Rochester L, Schott JM, Limousin P, Burn D, Rossor MN, Hariz M, Jahanshahi M, Foltynie T. Bilateral nucleus basalis of Meynert deep brain stimulation for dementia with Lewy bodies: A randomised clinical trial. Brain Stimul. 2020 Jul-Aug;13(4):1031-1039. doi: 10.1016/j.brs.2020.04.010. Epub 2020 Apr 22.
Results Reference
derived
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Deep Brain Stimulation for Patients With Dementia With Lewy Bodies
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