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N/A N=290 Randomized Single-blind Health Services Research

REVEAL III: Risk Evaluation and Education for Alzheimer's Disease

Alzheimer Disease

Enrolled (actual)
290
Serious AEs
0.4%
Results posted
Sep 2014
Primary outcome: Primary: Center for Epidemiological Studies-Depression Scale (CES-D) — 4.8; 7.0; 6.4; 5.5 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Pleiotropic info, in-person disclosure (Behavioral); AD-only info, in-person disclosure (Behavioral); Pleiotropic info, phone disclosure (Behavioral); AD-only info, phone disclosure (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Brigham and Women's Hospital
Primary completion
Oct 2009

Outcome Measures

OutcomeResultp-value
PRIMARY
Center for Epidemiological Studies-Depression Scale (CES-D)
4.8; 7.0; 6.4; 5.5; 5.5; 6.6
PRIMARY
Beck Anxiety Inventory (BAI)
2.9; 4.1; 3.2; 3.1; 3.4; 3.4
SECONDARY
Impact of Events Scale (IES)
3.4; 4.5; 3.7; 3.8; 3.5; 4.0

Summary

The purpose of this study is to provide healthy adults with genetic testing and information about their chances of developing Alzheimer's disease.

Eligibility Criteria

Inclusion Criteria

  • Aged 18 years to 85 years old

Exclusion Criteria

  • Unable to visit a study site
  • Current untreated depression or anxiety
  • Family history of AD diagnosed under age 60
  • More than one first-degree relative diagnosed with AD (e.g. Mother and brother)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00462917). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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