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Methylphenidate for Apathy in Alzheimer's Dementia: A Controlled Study

Primary Purpose

Alzheimer's Disease, Apathy, Dementia

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Methylphenidate
Placebo
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alzheimer's Disease focused on measuring Alzheimer's Disease, Apathy, Dementia, Methylphenidate

Eligibility Criteria

55 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Diagnosis of dementia of the Alzheimer type (DSM-IV Text Revision (TR) criteria)
  2. Mini-mental state examination (MMSE) >18, but <29
  3. Apathy Evaluation Scale (AES) score of more than 40
  4. Ability to provide informed consent by either the patient or caregiver.
  5. If subjects are being treated with antidepressants, they should be on a stable dose of antidepressants for at least two months prior to the enrollment into the study.
  6. If subjects are being treated with cholinesterase inhibitors and memantine, they should be on stable dose of those medications at least four months prior to the enrollment into the study.

Exclusion Criteria:

  1. Patient currently taking methylphenidate or hypersensitivity or prior significant adverse events with methylphenidate.
  2. Patients currently taking Adderall (amphetamine mixed salts) or Dexedrine (dextroamphetamine sulphate) or any other amphetamine product.
  3. Uncontrolled hypertension (BP > 140/90) or tachycardia (100) at screening visit
  4. Patients with frontotemporal dementia
  5. Patients meeting criteria for Major Depressive Disorder on the Mini International Neuropsychiatric Inventory (MINI)
  6. Patients with active psychosis as determined by MINI
  7. Patients currently being treated with antipsychotics
  8. History of uncontrolled seizure disorder
  9. History of malignant hypertension, symptomatic cardiovascular disease, cardiomyopathy, known structural cardiac defect or medically unstable arrhythmias.
  10. History of Tourette's syndrome or presence of motor tics
  11. Patients with glaucoma
  12. Patients taking monoamine oxidase inhibitors (MAOIs)
  13. Patient taking clonidine

Sites / Locations

  • VA Medical Center, Omaha

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Arm 1

Arm 2

Arm Description

Methylphenidate

Placebo

Outcomes

Primary Outcome Measures

Apathy Evaluation Scale Score at 12 Weeks
The Apathy Evaluation Scale (AES) has been specifically developed to assess apathy and discriminate it from depression. This 18 item scale with score ranging from 18 to 72, assesses apathy in behavioral, cognitive and emotional domains over the previous four weeks. Higher scores indicate worsening apathy.

Secondary Outcome Measures

Mini-mental State Examination (MMSE) at 12 Weeks
Mini-mental State Examination (MMSE) is a commonly used screening measure for cognition with questions pertaining to orientation, registration, recall, visuo-spatial construction, attention span etc. Score on MMSE ranges from 0-30, higher scores indicating improving cognition
Clinical Global Impression
The Clinical Global Impression scale is an observational scale of global evaluation, which assesses the change in degree of illness in relation to the original assessment. The severity sub-scale reported below ranges from 1-7 wherein higher scores indicate worsening severity of illness.

Full Information

First Posted
July 2, 2007
Last Updated
October 19, 2015
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT00495820
Brief Title
Methylphenidate for Apathy in Alzheimer's Dementia: A Controlled Study
Official Title
Methylphenidate for Apathy in Alzheimer's Dementia: A Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2015
Overall Recruitment Status
Completed
Study Start Date
August 2007 (undefined)
Primary Completion Date
March 2010 (Actual)
Study Completion Date
June 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is to determine the efficacy of methylphenidate over placebo in treating apathy in patients with Alzheimer's dementia. Apathy is one of the earliest and most profound disturbances that occur in Alzheimer's dementia (AD). Hypotheses: 1. Methylphenidate (MPH) will improve apathy significantly more than placebo in AD. 2. Successful treatment of apathy will improve Instrumental Activities of Daily Living (IADLs), and caregiver burden.
Detailed Description
Objective: Apathy is one of the earliest and most profound disturbances that occur in Alzheimer's dementia (AD). Based on promising preliminary data from our open-label pilot study we propose a double blind, placebo-controlled randomized clinical trial of methylphenidate for treatment of apathy in AD. Research Design: Randomized double blind, placebo-controlled study which will evaluate the effect of methylphenidate on apathy and also the impact of improvement of apathy on caregiver burden and functional status. Hypotheses: 1. Methylphenidate will improve apathy significantly more than placebo in AD. 2. Successful treatment of apathy will improve Instrumental Activities of Daily Living (IADLs), and caregiver burden. Methodology: 60 patients with apathy in the context of AD will be recruited over the next three years. In our proposed study patients will be recruited from relevant clinics at the Omaha Veterans Affairs Medical Center (VAMC) including clinics in Geriatric Psychiatry, Neurology, Primary Care and Geriatric Medicine. 30 patients each with AD and apathy will be randomly assigned to placebo or MPH. All patients in the methylphenidate arm will be started at 5mg twice daily and titrated to 10mg twice daily at two weeks. Patients will be continued in this arm for 12 weeks followed by a 2-week discontinuation phase. Patients will be assessed on regular intervals using the Apathy Evaluation Scale, Instrumental Activities of Daily Living, Zarit Burden Scale and Mini Mental State Examination. Findings: None, the study is not complete. Clinical Relationships: While memory is the key cognitive problem in AD, apathy is the key behavioral problem. Apathy is characterized by indifference, disengagement, passivity, and lack of enthusiasm, interest, empathy and interpersonal involvement. Apathy is the most common, one of the earliest and probably the most persistent of behavioral problems in AD. Apathy is the most disturbing behavior to caregivers and has the greatest impact on functional status and caregiver burden. Despite this, apathy as a behavioral problem has largely been neglected. Most of the research directed towards behavioral problems in dementia is targeted towards more visible behaviors such as agitation, and psychosis. Remarkably, there are no published randomized, double blind, placebo controlled studies in the treatment of apathy associated with AD. Impact/Significance: Around 1.4 million veterans suffer from apathy in association with AD. Apathy is a strong predictor for functional decline and caregiver burden. Treatment of apathy is remarkably understudied and is absolutely critical to allow veterans to maximize their functional status, social engagement and quality of life, and thus delaying placement in assisted living or nursing home settings.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer's Disease, Apathy, Dementia
Keywords
Alzheimer's Disease, Apathy, Dementia, Methylphenidate

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm 1
Arm Type
Experimental
Arm Description
Methylphenidate
Arm Title
Arm 2
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Drug
Intervention Name(s)
Methylphenidate
Other Intervention Name(s)
Ritalin
Intervention Description
Subject will receive 5mg twice a day for two weeks then 10mg twice a day until week 12 of the study.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Standard inactive pill.
Primary Outcome Measure Information:
Title
Apathy Evaluation Scale Score at 12 Weeks
Description
The Apathy Evaluation Scale (AES) has been specifically developed to assess apathy and discriminate it from depression. This 18 item scale with score ranging from 18 to 72, assesses apathy in behavioral, cognitive and emotional domains over the previous four weeks. Higher scores indicate worsening apathy.
Time Frame
At 12 weeks
Secondary Outcome Measure Information:
Title
Mini-mental State Examination (MMSE) at 12 Weeks
Description
Mini-mental State Examination (MMSE) is a commonly used screening measure for cognition with questions pertaining to orientation, registration, recall, visuo-spatial construction, attention span etc. Score on MMSE ranges from 0-30, higher scores indicating improving cognition
Time Frame
At 12 weeks
Title
Clinical Global Impression
Description
The Clinical Global Impression scale is an observational scale of global evaluation, which assesses the change in degree of illness in relation to the original assessment. The severity sub-scale reported below ranges from 1-7 wherein higher scores indicate worsening severity of illness.
Time Frame
At 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of dementia of the Alzheimer type (DSM-IV Text Revision (TR) criteria) Mini-mental state examination (MMSE) >18, but <29 Apathy Evaluation Scale (AES) score of more than 40 Ability to provide informed consent by either the patient or caregiver. If subjects are being treated with antidepressants, they should be on a stable dose of antidepressants for at least two months prior to the enrollment into the study. If subjects are being treated with cholinesterase inhibitors and memantine, they should be on stable dose of those medications at least four months prior to the enrollment into the study. Exclusion Criteria: Patient currently taking methylphenidate or hypersensitivity or prior significant adverse events with methylphenidate. Patients currently taking Adderall (amphetamine mixed salts) or Dexedrine (dextroamphetamine sulphate) or any other amphetamine product. Uncontrolled hypertension (BP > 140/90) or tachycardia (100) at screening visit Patients with frontotemporal dementia Patients meeting criteria for Major Depressive Disorder on the Mini International Neuropsychiatric Inventory (MINI) Patients with active psychosis as determined by MINI Patients currently being treated with antipsychotics History of uncontrolled seizure disorder History of malignant hypertension, symptomatic cardiovascular disease, cardiomyopathy, known structural cardiac defect or medically unstable arrhythmias. History of Tourette's syndrome or presence of motor tics Patients with glaucoma Patients taking monoamine oxidase inhibitors (MAOIs) Patient taking clonidine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Prasad R. Padala
Organizational Affiliation
VA Medical Center, Omaha
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Medical Center, Omaha
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68105-1873
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
20220576
Citation
Padala PR, Burke WJ, Shostrom VK, Bhatia SC, Wengel SP, Potter JF, Petty F. Methylphenidate for apathy and functional status in dementia of the Alzheimer type. Am J Geriatr Psychiatry. 2010 Apr;18(4):371-4. doi: 10.1097/JGP.0b013e3181cabcf6.
Results Reference
result
PubMed Identifier
28945120
Citation
Padala PR, Padala KP, Lensing SY, Ramirez D, Monga V, Bopp MM, Roberson PK, Dennis RA, Petty F, Sullivan DH, Burke WJ. Methylphenidate for Apathy in Community-Dwelling Older Veterans With Mild Alzheimer's Disease: A Double-Blind, Randomized, Placebo-Controlled Trial. Am J Psychiatry. 2018 Feb 1;175(2):159-168. doi: 10.1176/appi.ajp.2017.17030316. Epub 2017 Sep 15.
Results Reference
derived

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Methylphenidate for Apathy in Alzheimer's Dementia: A Controlled Study

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