Status:

COMPLETED

Rhythm Experience and Africana Culture Trial

Lead Sponsor:

University of Pittsburgh

Collaborating Sponsors:

National Institute on Aging (NIA)

Conditions:

Cognitive Performance

Brain Structure

Eligibility:

All Genders

60-80 years

Phase:

NA

Brief Summary

REACT is a randomized intervention to examine the benefits of African Dance as a method to increase physical activity behaviors in older adults. In this 6- month intervention, older African Americans ...

Detailed Description

Aim 1: Examine whether the African Dance intervention improves cognitive performance compared to an educational control group. H1: The dance group will show cognitive improvements in a domain-specific...

Eligibility Criteria

Inclusion

  • self identifies race as African American
  • between 60 and 80 years of age
  • ambulatory without pain or the assistance of walking devices
  • no history of falls or balance problems
  • able to speak and read English
  • available during the times classes are offered and able to make at least 80% of classes (e.g., no long-term travel plans)
  • reliable means of transportation
  • scores above the range on the Brief Telephone Interview for Cognitive Status (TICS) indicative of moderate to severe cognitive impairment (scores 21 or above)
  • no diagnosis of a neurological disease or psychiatric conditions
  • eligible to undergo MRI (not claustrophobic and no metal or history of injury involving metal).
  • Fully vaccinated for coronavirus disease (COVID-19).

Exclusion

  • self identifies race as other than African American
  • not between 60 and 80 years of age
  • not ambulatory without pain or the assistance of walking devices
  • history of falls or balance problems
  • unable to speak and read English
  • unavailable during the times classes are offered or unable to make at least 80% of classes (e.g., indicates long-term travel plans during intervention period)
  • no reliable means of transportation
  • scores in range on the TICS indicative of moderate to severe cognitive impairment (scores 21 or below)
  • has a diagnosis of a neurological disease or psychiatric condition
  • ineligible to undergo MRI (claustrophobic and/or metal in body or history of injury involving metal).

Key Trial Info

Start Date :

May 21 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 16 2024

Estimated Enrollment :

151 Patients enrolled

Trial Details

Trial ID

NCT03771716

Start Date

May 21 2019

End Date

August 16 2024

Last Update

August 13 2025

Active Locations (1)

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1

University of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15260