PPS: Implementing a Physical and Cognitive Performance Assessment Cohort in the MURDOCK Study Community Registry and Biorepository

Sponsor
Duke University (Other)
Overall Status
Completed
CT.gov ID
NCT01720472
Collaborator
(none)
1,000
6
75.9
166.7
2.2

Study Details

Study Description

Brief Summary

The purpose of this study is to use the MURDOCK Horizon 1.5 infrastructure (Duke Instutional Review Board Pro00011196) to specifically target and enroll 1,000 participants across age groups and other demographic categories in order to develop a diverse cohort with specific physical and cognitive performance data paired with biological samples.

Condition or Disease Intervention/Treatment Phase
  • Genetic: Biomarker studies

Detailed Description

The MURDOCK Study, proposes this Horizon 2 study to collect a brief physical and cognitive performance assessment from 1,000 MURDOCK Registry participants. Blood sample aliquots will also be obtained. These physical and cognitive performance data, paired with -omics data from plasma and serum sample analyses, offer promise in the discovery of biomarkers for functional decline. This research will provide an important basis for our understanding of the physical, lifestyle, and genetic factors which, over the lifespan, contribute to changes in physical and cognitive capabilities as we age.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
1000 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Implementing a Physical and Cognitive Performance Assessment Cohort in the MURDOCK Study Community Registry and Biorepository
Study Start Date :
May 1, 2012
Actual Primary Completion Date :
Aug 28, 2018
Actual Study Completion Date :
Aug 28, 2018

Arms and Interventions

Arm Intervention/Treatment
Community, Physical Performance

Genetic: Biomarker studies

Outcome Measures

Primary Outcome Measures

  1. Implementing a Physical and Cognitive Performance Assessment Cohort in the MURDOCK Study Community Registry and Biorepository [Upto 2 years or 24 months]

    Factors associated with physical function and physical activity and change in physical activity and function over two-year follow-up.

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • A resident of Cabarrus County and/or the city of Kannapolis (and surrounding regions) or certain portions of Rowan, Mecklenburg, or Stanly counties in North Carolina for 6 or more months of the year.

  • Age 30 or older

Exclusion Criteria:
  • Female that is currently pregnant

  • Having had a heart attack, angina, congestive heart failure, or fluid in the lungs within the past 6 months

  • Participant that requires consent by a legally authorized representative

  • Participant that cannot walk 30ft without human assistance

Contacts and Locations

Locations

Site City State Country Postal Code
1 Bethesda Health Center Charlotte North Carolina United States 28262
2 McGill Family Medicine Concord North Carolina United States 28025
3 Carolinas Medical Center NorthEast Medical Arts Building Concord North Carolina United States 28205
4 Ada Jenkins Center Davidson North Carolina United States 28036
5 Harrisburg Sleep Center Harrisburg North Carolina United States 28075
6 Lake Norman Community Health Clinic Huntersville North Carolina United States 28078

Sponsors and Collaborators

  • Duke University

Investigators

  • Principal Investigator: Miriam C Morey, Ph.D., Duke University

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Duke University
ClinicalTrials.gov Identifier:
NCT01720472
Other Study ID Numbers:
  • Pro00036608
First Posted:
Nov 2, 2012
Last Update Posted:
Jan 31, 2019
Last Verified:
Jan 1, 2019

Study Results

No Results Posted as of Jan 31, 2019