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SeniorWISE: Improving Everyday Memory in At-Risk Elderly

This study has been completed.
Information provided by National Institute on Aging (NIA)

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Descriptive Information Fields
Brief Title  SeniorWISE: Improving Everyday Memory in At-Risk Elderly
Official Title  Improving Everyday Memory in At-Risk Elderly
Brief Summary

The purpose of this study is to determine whether classes on memory training will help older adults to improve or maintain their daily activities.

Detailed Description

Volunteer participants will be randomly assigned to experimental (memory training) and comparison (health promotion) groups. Both groups will learn strategies for successful aging. Participants will be in the study for 27 months and will be interviewed on five occasions for 3 hours per interview. The classroom-based intervention is an 8-session, 1 1/2 hour course designed to teach older adults the use of strategies to improve everyday memory. Strategically-placed booster sessions will be provided to subjects within 3 months following the last class session.

Study Phase Phase III
Study Type  Interventional
Study Design  Educational/Counseling/Training, Randomized
Primary Outcome Measure 
Secondary Outcome Measure 
Condition  Aging
Intervention  Procedure: Memory Training
MEDLINE PMIDs 12813430,   11840404,   11987351,   15481070
Links About the SeniorWISE Study This link exits the ClinicalTrials.gov site
Recruitment Information Fields
Recruitment Status  Completed
Enrollment  260
Start Date  March 2001
Completion Date February 2006
Eligibility Criteria 

Inclusion Criteria:

  • Reside in Austin, Texas or Travis County
  • African, Caucasian, or Hispanic heritage
  • Fluent in reading and speaking English
  • Mini Mental Exam scores of 23-30
  • Pass executive function test
  • Adequate hearing and vision to enable participation in classroom learning
  • Free of Alzheimer's disease or other conditions (e.g., certain cancers) likely to result in mortality before study completion

Exclusion Criteria:

  • Under 65
  • Score less than 23 on MMSE
  • Fail the executive function tests
  • Severe sensory losses, hearing or vision, that would prohibit testing or participation
  • self-report a diagnosis of Alzheimer's disease or other conditions (e.g., certain cancers) likely to result in mortality before study completion
Gender Both
Ages 65 Years and older
Accepts Healthy Volunteers Yes
Contacts ††
Location Countries  United States
Administrative Information Fields
NCT ID  NCT00094731
Organization ID AG0008
Secondary IDs †† R01 AG15384
Study Sponsor  National Institute on Aging (NIA)
Collaborators ††
Investigators 
Principal Investigator:     Graham McDougall, PhD, RN     University of Texas at Austin, School of Nursing    
Information Provided By National Institute on Aging (NIA)
Verification Date February 2006
First Received Date  October 21, 2004
Last Updated Date February 23, 2006

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




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