The Baltimore Experience Corps Study
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ClinicalTrials.gov Identifier: NCT00380562 |
Recruitment Status :
Completed
First Posted : September 26, 2006
Last Update Posted : September 19, 2013
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Tracking Information | ||||
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First Submitted Date ICMJE | September 25, 2006 | |||
First Posted Date ICMJE | September 26, 2006 | |||
Last Update Posted Date | September 19, 2013 | |||
Study Start Date ICMJE | July 2006 | |||
Actual Primary Completion Date | December 2011 (Final data collection date for primary outcome measure) | |||
Current Primary Outcome Measures ICMJE |
Decreased disability in mobility and Instrumental Activities of Daily Living (IADL) [ Time Frame: Measured in 4 month intevals from baseline to 24 month ] Walking speed, chair stands, questionnaires related to mobility and activities
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Original Primary Outcome Measures ICMJE |
Decreased disability in mobility and Instrumental Activities of Daily Living (IADL) | |||
Change History | ||||
Current Secondary Outcome Measures ICMJE |
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Original Secondary Outcome Measures ICMJE |
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Current Other Pre-specified Outcome Measures | Not Provided | |||
Original Other Pre-specified Outcome Measures | Not Provided | |||
Descriptive Information | ||||
Brief Title ICMJE | The Baltimore Experience Corps Study | |||
Official Title ICMJE | Experience Corps Trial: Improving Health of Older Populations Through Generativity | |||
Brief Summary | The purpose of this study is to examine the effectiveness of the Experience Corps program in preventing or delaying physical disability in older adults, by studying the effects of volunteerism on physical, social and cognitive well-being. | |||
Detailed Description | The Baltimore Experience Corps Study is a randomized, controlled, community-based trial of the effectiveness of Experience Corps (EC) to determine if participation for adults 60 years and older, over two years of follow-up, results in better outcomes in the EC versus control arm in terms of mobility, strength, balance, and cognitive functioning. The Experience Corps is a community-based model for health promotion for older adults embedded within a social engagement program. The program places older adult volunteers in meaningful roles in public elementary schools, bringing the time, experience, and wisdom of older adults to bear in improving academic and behavioral outcomes of children. The Experience Corps incorporates health promotion preventing disability and dependency associated with aging, into new, generative roles for older adults. This program was initially designed by Dr. Linda Fried of this application, along with Marc Freedman of Civic Ventures, Inc. It has gone through two national demonstrations, neither of which evaluated the impact on older adults. |
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Study Type ICMJE | Interventional | |||
Study Phase ICMJE | Not Applicable | |||
Study Design ICMJE | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Single (Investigator) Primary Purpose: Treatment |
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Condition ICMJE |
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Intervention ICMJE | Behavioral: Experience Corps
High intensity volunteering (15 hours a week or more) over a two year time period working with children in grades K-3 in Baltimore City Schools. Controls are assigned to usual activities for two years and then offered opportunity to volunteer with children at the end of two year.
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Study Arms ICMJE |
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Publications * |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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Recruitment Information | ||||
Recruitment Status ICMJE | Completed | |||
Actual Enrollment ICMJE |
702 | |||
Original Enrollment ICMJE |
1046 | |||
Actual Study Completion Date ICMJE | December 2011 | |||
Actual Primary Completion Date | December 2011 (Final data collection date for primary outcome measure) | |||
Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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Sex/Gender ICMJE |
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Ages ICMJE | 60 Years and older (Adult, Older Adult) | |||
Accepts Healthy Volunteers ICMJE | Yes | |||
Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | |||
Listed Location Countries ICMJE | United States | |||
Removed Location Countries | ||||
Administrative Information | ||||
NCT Number ICMJE | NCT00380562 | |||
Other Study ID Numbers ICMJE | AG0069 P01AG027735 ( U.S. NIH Grant/Contract ) |
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Has Data Monitoring Committee | Yes | |||
U.S. FDA-regulated Product | Not Provided | |||
IPD Sharing Statement ICMJE | Not Provided | |||
Current Responsible Party | George W. Rebok, PhD, Johns Hopkins University | |||
Original Responsible Party | Not Provided | |||
Current Study Sponsor ICMJE | Johns Hopkins University | |||
Original Study Sponsor ICMJE | National Institute on Aging (NIA) | |||
Collaborators ICMJE |
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Investigators ICMJE |
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PRS Account | Johns Hopkins University | |||
Verification Date | September 2013 | |||
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |