The Baltimore Experience Corps Study
Recruitment status was Recruiting
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Purpose
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.
| Condition | Intervention |
|---|---|
|
Aging Generativity |
Behavioral: Experience Corps |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Single Blind Primary Purpose: Treatment |
| Official Title: | Experience Corps Trial: Improving Health of Older Populations Through Generativity |
- Decreased disability in mobility and Instrumental Activities of Daily Living (IADL)
- Decreased falls
- decreased rate of decline in memory
- increased, preserved or slowed decline in strength, balance, walking speed, frailty, timed "get up and go", cortical plasticity and executive function and speed and accuracy in objective IADL task performance
| Estimated Enrollment: | 1046 |
| Study Start Date: | March 2006 |
| Estimated Study Completion Date: | March 2011 |
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 the Principal Investigator 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.
Eligibility| Ages Eligible for Study: | 60 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- 60 years or older
- Agree to commit to at least 1 year of participation in the EC and to participate at least 15 hours per week for the full school year, if randomized to the intervention group
- Meet minimum criteria for cognitive functioning necessary to function successfully in a school setting
- Functionally literate, using a nationally recognized and standardized evaluation which provides grade level equivalency in reading and spelling
- Ability to travel to the schools, if randomized to the intervention group
- Agree to accept randomization and to participate in evaluations
- Clearance on the Baltimore city public school's criminal background check, if randomized to intervention group
- Complete training, if randomized to intervention group
Exclusion Criteria:
- Under 60 years of age
Contacts and Locations| Contact: Gene Graves | 410-807-1785 | cgraves1@jhmi.edu |
| Contact: Carol Ray | 410-818-8348 | cray9@jhmi.edu |
| United States, Maryland | |
| Center on Aging and Health | Recruiting |
| Baltimore, Maryland, United States, 21205 | |
| Contact: Laprisha Berry-Vaughn, MSW, MPH 410-502-6630 lberry7@jhmi.edu | |
| Sub-Investigator: Jeremy Barron, MD | |
| Sub-Investigator: Michelle Carlson, PhD | |
| Sub-Investigator: Constantine Frangakis, PhD | |
| Sub-Investigator: Tara Gruenewald, PhD | |
| Sub-Investigator: Barbara Martin, PhD | |
| Sub-Investigator: Iveris Martinez, PhD | |
| Sub-Investigator: George Rebok, PhD | |
| Sub-Investigator: Teresa Seeman, PhD | |
| Sub-Investigator: Erwin Tan, PhD | |
| Sub-Investigator: Elizabeth Tanner, PhD, RN | |
| Sub-Investigator: Keith Whitfield, PhD | |
| Sub-Investigator: Qilu Yu, PhD | |
| Principal Investigator: | Linda Fried, MD, MPH | Johns Hopkins University |
| Study Director: | Laprisha Berry-Vaughn | Johns Hopkins University |
More Information
Publications:
| ClinicalTrials.gov Identifier: | NCT00380562 History of Changes |
| Other Study ID Numbers: | AG0069, PO1AG027735 |
| Study First Received: | September 25, 2006 |
| Last Updated: | January 29, 2009 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Institute on Aging (NIA):
|
Quality of life Cognitive Functioning Activities of Daily Living Disability prevention |
ClinicalTrials.gov processed this record on June 18, 2013