Risk Evaluation and Education for Alzheimer's Disease (REVEAL I)
Primary Purpose
Alzheimer's Disease
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
APOE Disclosure
Sponsored by
About this trial
This is an interventional health services research trial for Alzheimer's Disease focused on measuring Mild Cognitive Impairment, disease/disorder proneness/risk, family genetics, genetic counseling, genetic marker, genetic polymorphism, genetic susceptibility
Eligibility Criteria
Inclusion Criteria:
- Adult children of a person with clinically diagnosed and/or autopsy-confirmed Alzheimer's disease
- 18 years or older
Exclusion Criteria:
- Current dementia
- Current untreated depression
Sites / Locations
- Boston University School of Medicine
- Weill Medical College of Cornell University
- Case Western Reserve University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
1
2
Arm Description
AD risk assessment based on family history and APOE genotype
AD risk assessment based on family history alone
Outcomes
Primary Outcome Measures
Center for Epidemiological Studies-Depression Scale (CES-D)
Beck Anxiety Inventory (BAI)
Secondary Outcome Measures
Impact of Events Scale (IES)
Future Attitudes Scale (FAS)
Positive and Negative Affect Schedule (PANAS)
Full Information
NCT ID
NCT00571025
First Posted
December 7, 2007
Last Updated
July 22, 2009
Sponsor
National Human Genome Research Institute (NHGRI)
Collaborators
National Institute on Aging (NIA)
1. Study Identification
Unique Protocol Identification Number
NCT00571025
Brief Title
Risk Evaluation and Education for Alzheimer's Disease
Acronym
REVEAL I
Official Title
Genetic Risk Assessment and Counseling for Alzheimer's Disease
Study Type
Interventional
2. Study Status
Record Verification Date
July 2009
Overall Recruitment Status
Completed
Study Start Date
August 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
April 2004 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
National Human Genome Research Institute (NHGRI)
Collaborators
National Institute on Aging (NIA)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine the characteristics of those who obtain genetic susceptibility testing for Alzheimer's disease with APOE disclosure and to study the psychological and behavioral consequences of providing this information.
Detailed Description
Advances in genetic research have led to an increased number of testing procedures to determine future risk of disease among at-risk individuals. An increasing number of genes are being identified that confer susceptibility for a given disease rather than inevitably causing it. Given that such genes may provide risk information for common diseases (e.g., stroke, depression), there is a growing need to understand how at-risk populations might respond to the option of genetic susceptibility testing. A prominent case in point is Alzheimer's disease (AD).
Participation in this study requires an initial phone call which will elicit some medical and family history information about the participant. A first in-person visit to the clinic will consist of an education session and the administration of some tests to assess memory and thinking skills. This visit will take approximately 2-3 hours. Approximately 2 weeks later, participants will return to have their blood drawn for genetic testing. Participants will then be randomized to one of two groups. Those in the experimental arm will receive information on their risk based on their family history and APOE genotype, while those in the active comparator arm will receive information on their risk for developing Alzheimer's disease based on their family history alone. Participants will be followed for 1 year following disclosure of results with 2 additional clinic visits.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer's Disease
Keywords
Mild Cognitive Impairment, disease/disorder proneness/risk, family genetics, genetic counseling, genetic marker, genetic polymorphism, genetic susceptibility
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
301 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
AD risk assessment based on family history and APOE genotype
Arm Title
2
Arm Type
Active Comparator
Arm Description
AD risk assessment based on family history alone
Intervention Type
Behavioral
Intervention Name(s)
APOE Disclosure
Intervention Description
Individuals are provided with a lifetime percentage risk of developing Alzheimer's disease and told their own APOE genotype.
Primary Outcome Measure Information:
Title
Center for Epidemiological Studies-Depression Scale (CES-D)
Time Frame
baseline, 6 weeks, 6 months, 12 months post-disclosure
Title
Beck Anxiety Inventory (BAI)
Time Frame
baseline, 6 weeks, 6 months, 12 months post-disclosure
Secondary Outcome Measure Information:
Title
Impact of Events Scale (IES)
Time Frame
6 weeks, 6 months, 12 months post-disclosure
Title
Future Attitudes Scale (FAS)
Time Frame
baseline, 6 weeks, 6 months, 12 months post-disclosure
Title
Positive and Negative Affect Schedule (PANAS)
Time Frame
baseline, 6 weeks, 6 months, 12 months post-disclosure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Adult children of a person with clinically diagnosed and/or autopsy-confirmed Alzheimer's disease
18 years or older
Exclusion Criteria:
Current dementia
Current untreated depression
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert C. Green, MD, MPH
Organizational Affiliation
Boston University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Boston University School of Medicine
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02118
Country
United States
Facility Name
Weill Medical College of Cornell University
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
Facility Name
Case Western Reserve University
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44120
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
9343467
Citation
Farrer LA, Cupples LA, Haines JL, Hyman B, Kukull WA, Mayeux R, Myers RH, Pericak-Vance MA, Risch N, van Duijn CM. Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium. JAMA. 1997 Oct 22-29;278(16):1349-56.
Results Reference
background
PubMed Identifier
9348421
Citation
Green RC, Clarke VC, Thompson NJ, Woodard JL, Letz R. Early detection of Alzheimer disease: methods, markers, and misgivings. Alzheimer Dis Assoc Disord. 1997;11 Suppl 5:S1-5; discussion S37-9. doi: 10.1016/s0197-4580(96)80334-4.
Results Reference
background
PubMed Identifier
11790212
Citation
Green RC, Cupples LA, Go R, Benke KS, Edeki T, Griffith PA, Williams M, Hipps Y, Graff-Radford N, Bachman D, Farrer LA; MIRAGE Study Group. Risk of dementia among white and African American relatives of patients with Alzheimer disease. JAMA. 2002 Jan 16;287(3):329-36. doi: 10.1001/jama.287.3.329.
Results Reference
background
PubMed Identifier
19605829
Citation
Green RC, Roberts JS, Cupples LA, Relkin NR, Whitehouse PJ, Brown T, Eckert SL, Butson M, Sadovnick AD, Quaid KA, Chen C, Cook-Deegan R, Farrer LA; REVEAL Study Group. Disclosure of APOE genotype for risk of Alzheimer's disease. N Engl J Med. 2009 Jul 16;361(3):245-54. doi: 10.1056/NEJMoa0809578.
Results Reference
derived
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Risk Evaluation and Education for Alzheimer's Disease
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