Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
Healthy Volunteers
ID07050589

A Community-Based Recreation Program to Improve Function and Quality of Life in Older Adults

Led by State University of New York at Buffalo · Updated on 2026-03-16

80

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying a community-based recreation program aimed at improving cognitive and physical function in older adults aged 60 and above. This trial evaluates the effects of weekly group artmaking combined with SMARTfit dual-task exergaming, delivered through the Buffalo-Niagara YMCA. The study focuses on changes in cognitive function and physical abilities over a 24-week period. Participants are randomly assigned to either receive the recreation-based program, which includes weekly exercise and art sessions, or to a control group that does not receive the program. The intervention involves a combination of group art activities and SMARTfit exergaming designed to engage both mind and body. During the study, participants undergo assessments of attention, balance, dual-task performance, and interference inhibition at enrollment, week 8, and week 16. The researchers monitor cognitive and physical outcomes to understand the program's impact. The total participation time spans 24 weeks with ongoing evaluations throughout the trial.

CONDITIONS

Brief Title

Group Recreation to Enhance Function Aging

Who Can Participate

Age: 60Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be 60 years of age or older
  • Have no more than mild cognitive impairment (MoCA score of 24 points or higher)
  • Have no contraindications to exercise as guided by the American College of Sports Medicine
  • Be fluent in English
Not Eligible

You will not qualify if you...

  • Have any condition preventing safe exercise participation as determined by the Physical Activity Readiness Questionnaire for Older Adults (PAR-OA)
  • Have severe neurological disease
  • Have severe psychiatric illness
  • Have a likelihood of withdrawing due to severe illness or a life expectancy under 6 months
  • Have experienced a lower or upper limb amputation
  • Have greater than mild cognitive impairment (MoCA score below 24 points)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

screening and enrollment visit

Outpatient Treatment

Duration - 16 weeks

Participants in the program group will attend weekly sessions involving dual-task exergaming and group art-making. Control participants will not receive the recreation-based program.

Weekly visits for up to 16 weeks

Trial Site Locations

Total: 1 location

1

Buffalo-Niagara YMCA

Buffalo, New York, United States, 14223

Actively Recruiting

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Research Team

N

Nikhil Satchidanand, PhD Exercise Physiology

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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