Rhythm Experience and Africana Culture Trial
REACT
2 other identifiers
interventional
151
1 country
1
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 will be randomly assigned to either an African Dance or an Africana Culture class. Both before and at the completion of the intervention, the investigators will collect a comprehensive neuropsychological battery and MRI scans of brain health and function to better study how physical activity influences neurocognitive health in African Americans.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started May 2019
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 30, 2018
CompletedFirst Posted
Study publicly available on registry
December 11, 2018
CompletedStudy Start
First participant enrolled
May 21, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 25, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 16, 2024
CompletedResults Posted
Study results publicly available
August 13, 2025
CompletedAugust 13, 2025
August 1, 2025
5.2 years
November 30, 2018
July 25, 2025
August 11, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Flanker Performance
A Flanker Inhibitory Control and Attention task will be administered at baseline, and then following the intervention (6 months). The main outcome from this task is the computed score from the NIH Toolbox, which reflects the participant's ability to inhibit responses to irrelevant information while focusing attention on a target stimulus. In each trial, participants make a directional response to a center arrow when the flanking arrows are arranged in congruent vs. incongruent direction from the center stimulus. The computed score combines accuracy and reaction time into a single performance metric, ranging from 0 to 10, with higher values indicating better performance. Group differences will be tested on this outcome.
Changes from baseline to 6-months
Secondary Outcomes (1)
Hippocampal Volume (mm3)
Changes from baseline to 6-months
Other Outcomes (44)
Change in Cognitive Function
Changes from baseline to 6-months
Medication Use
Changes from baseline to 6-months
Cardiorespiratory Fitness
Changes from baseline to 6-months
- +41 more other outcomes
Study Arms (2)
African Dance
EXPERIMENTALThis is the experimental group. Dance classes will be held 3 times per week for 1 hour. Participants will learn traditional Africana dance moves and sequences.
African Cultural Immersion
ACTIVE COMPARATORThis is the active control group. Participants will participate in a variety of educational activities related to African Culture, including traditional cooking, lectures, crafts, music and films. They will meet 3 times per week for the same duration as the Dance group. However, they will not participate in aerobic activity during the classes, and most activities will be conducted in a seated position.
Interventions
Basic principles and guidelines for exercise programming will be followed including adequate warm-up and cool-down, progressive and gradual increments in duration, and instruction regarding avoidance of physical activity (PA) related injury. The African dance group will receive moderate intensity dance 1 hour per day, twice per week, for 6 months. The prescribed intensity will begin at light to moderate and progress to a moderate to high intensity level. Frequent assessment of heart rate and ratings of perceived exertion will ensure appropriate levels of intensity during each dance session. Levels of exertion during the dance will be prescribed and monitored based on baseline assessments of heart rate and cardiorespiratory fitness.
The Culture group will participate in activities, including cooking, art and games, music, traditional crafts, and lectures and discussions about other aspects of Africana culture and customs. Topics will vary from session to session to maintain interest and engagement. The sessions will be held in a small group format and will be lead my personnel with training in each topic. Participants will meet 1 hour per day, 3 times per week, for 6 months.
Eligibility Criteria
You may qualify if:
- 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).
You may not qualify if:
- 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).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Pittsburghlead
- National Institute on Aging (NIA)collaborator
Study Sites (1)
University of Pittsburgh
Pittsburgh, Pennsylvania, 15260, United States
Results Point of Contact
- Title
- Dr. Kirk I. Erickson
- Organization
- AdventHealth Research Institute
Study Officials
- PRINCIPAL INVESTIGATOR
Kirk I Erickson, PhD
University of Pittsburgh
Publication Agreements
- PI is Sponsor Employee
- No
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- Neither the investigator, nor outcomes assessors will know participants' group assignments. Participants will be instructed to refrain from speaking about their group's activities when visiting the lab for follow-up assessment. In addition, special care was taken to ensure that non-blinded laboratory staff (e.g., staff member notifying participants of their group assignments, staff monitoring the intervention classes) are not located in the same proximity in the laboratory, further preventing accidental unblinding.
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
November 30, 2018
First Posted
December 11, 2018
Study Start
May 21, 2019
Primary Completion
July 25, 2024
Study Completion
August 16, 2024
Last Updated
August 13, 2025
Results First Posted
August 13, 2025
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will not share