Dementia Clinical Trial
— IMPACT2Official title:
Implications for Management of PET Amyloid Classification Technology in the Imaging Dementia(IDEAS) Trial
NCT number | NCT02781220 |
Other study ID # | IMPACT-2 |
Secondary ID | |
Status | Active, not recruiting |
Phase | |
First received | |
Last updated | |
Start date | July 2016 |
Est. completion date | July 2021 |
Verified date | January 2020 |
Source | University of Utah |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The main purpose of this study is to build upon the evidence captured in the Imaging Dementia - Evidence for Amyloid Scanning (IDEAS; NCT02420756) trial to include valuable information regarding patient-reported outcomes and physician confidence in diagnosis and management based on the Implications for Management of PET Amyloid Classification Technology (IMPACT; NCT number not yet assigned) trial design.
Status | Active, not recruiting |
Enrollment | 69 |
Est. completion date | July 2021 |
Est. primary completion date | July 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 65 Years and older |
Eligibility |
Inclusion Criteria: - 65 and older; - Medicare beneficiary; - Diagnosis of mild cognitive impairment (MCI) or dementia, according to Diagnostic and Statistical Manual - IV (DSM-IV) and/or National Institutes of Aging-Alzheimer's Association criteria, verified by a dementia specialist within 24 months (American Psychiatric Association. 2000; McKhann et al. 2011; Albert et al. 2011); - Meets AUC: - Cognitive complaint verified by objectively confirmed cognitive impairment; - The etiologic cause of cognitive impairment is uncertain after a comprehensive evaluation by a dementia specialist, including general medical and neurological examination, mental status testing including standard measures of cognitive impairment, laboratory testing, and structural neuroimaging as below; - Alzheimer's disease is a diagnostic consideration; - Knowledge of amyloid PET status is expected to alter diagnosis and management. - Head MRI and/or CT within 24 months prior to enrollment; - Clinical laboratory assessment within the 12 months prior to enrollment: complete blood count (CBC), standard blood chemistry profile, thyroid stimulating hormone (TSH); vitamin B12; - Able to tolerate amyloid PET required by protocol, to be performed at a participating PET facility; - English or Spanish speaking (for the purposes of informed consent); - Willing and able to provide consent. Consent may be by proxy. Exclusion Criteria: - Normal cognition or subjective complaints that are not verified by cognitive testing. - Knowledge of amyloid status, in the opinion of the referring dementia expert, may cause significant psychological harm or otherwise negatively impact the patient or family. - Scan is being ordered solely based on a family history of dementia, presence of apolipoprotein E, or in lieu of genotyping for suspected autosomal mutation carriers. - Scan being ordered for nonmedical purposes (e.g., legal, insurance coverage, or employment screening). - Cancer requiring active therapy (excluding non-melanoma skin cancer); - Hip/pelvic fracture within the 12 months prior to enrollment; - Body weight exceeds PET scanner weight limit; - Life expectancy less than 24 months based on medical co-morbidities; - Residence in a skilled nursing facility. |
Country | Name | City | State |
---|---|---|---|
United States | Center for Alzheimer's Care, Imaging & Research | Salt Lake City | Utah |
Lead Sponsor | Collaborator |
---|---|
University of Utah |
United States,
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* Note: There are 58 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change in the interpretation of amyloid PET scans with semi-quantitative image analysis | Difference in a 5-point measure of amyloid scan positivity between a qualitative and semi-quantitative image analysis | within 30 days post amyloid PET scan | |
Primary | Percentage of change in care practices after amyloid PET scan | % of 13 care practices that differ before and after the amyloid PET scan | Visit 1, 30 days prior to scan and Visit 4, 90 days after scan | |
Secondary | Percentage of change in drug management options after amyloid PET | % of drug management options that differ before and after the amyloid PET scan | Visit 1, 30 days prior to scan and Visit 4, 90 days after scan | |
Secondary | Change in % likelihood of Alzheimer's disease (AD) diagnosis after amyloid PET scan | Difference in % of AD likelihood identified before and after the amyloid PET scan | Visit 1, 30 days prior to scan and Visit 4, 90 days after scan | |
Secondary | Percentage of change in leading diagnosis after amyloid PET | % of leading diagnosis that differ before and after amyloid PET scan | Visit 1, 30 days prior to scan and Visit 4, 90 days after scan | |
Secondary | Change in physician confidence in leading diagnosis | Difference in 5-point scale of physician confidence in leading diagnosis before and after amyloid PET scan | Visit 1, 30 days prior to scan and Visit 4, 90 days after scan | |
Secondary | Change in care partner's confidence in diagnosis after amyloid PET | Difference in 5-point scale of care partner confidence in diagnosis before and after amyloid PET scan | Visit 1, 30 days prior to scan, Visit 4, 90 days after scan, Visit 5, 180 days after scan and Visit 6, 270 days after scan | |
Secondary | Change in care partner satisfaction with evaluation after amyloid PET | Difference in 5-point scale of care partner satisfaction before team care and after amyloid PET scan | Visit 1, 30 days prior to scan and Visit 4, 90 days after scan | |
Secondary | Change in care partner assessment of the quality of evaluation after amyloid PET | Difference in 5-point scale of care partner quality before team care and after amyloid PET scan | Visit 1, 30 days prior to scan and Visit 4, 90 days after scan | |
Secondary | Proportion of care partners finding amyloid PET scan worthwhile | Proportion of care partners indicating they would agree to do an amyloid PET again on a yes/no/don't know scale | Visit 4, 90 days after scan | |
Secondary | Proportion exhibiting increased behavior disturbance during amyloid scan visit | % of patients showing a difference in the 44-point Catastrophic Reaction Scale between the median value in all non-scan visits and the value in the amyloid PET scan visit | Visit 1, Visit 2, Visit 3, and Visit 4 90 days post scan | |
Secondary | Percentage of change exhibiting increased behavior disturbance when the diagnosis is given | % of patients showing a difference in the 44-point Catastrophic Reaction Scale between Visit 1 and Visit 3 when learning the result of the scan | Visit 1, Visit 3, 60 days | |
Secondary | Care partner's sustained confidence in diagnosis received after amyloid PET scan | Care partner confidence in diagnosis received after amyloid PET scan on a 5-point scale | Visit 4, Visit 5, and Visit 6, 270 days post scan | |
Secondary | Care partner's sustained confidence in ability to adhere to management plan received after amyloid PET scan | Care partner confidence in ability to follow management plan outlined by physician after amyloid PET scan on a 5-point scale | Visit 4, Visit 5, and Visit 6, 270 days post scan | |
Secondary | Percentage of recommended care practices adhered to after amyloid PET scan | % of care practices recommended after amyloid PET scan reported by care partner | Visit 4, Visit 5, and Visit 6, 270 days post scan | |
Secondary | Percentage of recommended drug management adhered to after amyloid PET scan | % of drug management options recommended after amyloid PET scan reported by care partner | Visit 4, Visit 5, and Visit 6, 270 days post scan |
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