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Recruiting NCT07050589

Group Recreation to Enhance Function Aging

No phase Interventional Physical Functioning Cognitive Functioning

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Exercise and art.
Who it may be relevant to
Registry conditions: Physical Functioning, Cognitive Functioning. Basic parameters: from 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

Investigators will develop and deliver a community-based recreation program, delivering group artmaking and group SMARTfit dual-task exergaming to community-dwelling older adults. The program will be delivered through the Buffalo-Niagara YMCA. Outcomes of interest are change in cognitive function and change in physical functioning, inresponse to 24 weeks of weekly training.

Interventions

  • Behavioral Exercise and art
    Weekly SMARTfit dual-task exergaming and group art-making

Primary outcome measures

  • Cognitive Function: Attention [Time frame: From enrollment to week 8 and then week 16]
Secondary outcome measures (3)
  • Balance [Time frame: From enrollment to week 8 and then week 16]
  • Dual-Task Performance [Time frame: From enrollment to week 8 and then week 16]
  • Cognitive Function: Interference Inhibition [Time frame: baseline to week 8, through week 16]

Eligibility criteria

Inclusion criteria

  • > = 60 years of age
  • have no more than MCI (MoCA score ≥ 24 points)
  • have no contraindications to exercise, guided by the American College of Sports Medicine
  • fluent in English

Exclusion criteria

  • have a condition that would prevent safe participation in the exercise, 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 from the study due to severe illness or a life expectancy of < 6 mo
  • have experienced a lower or upper limb amputation
  • have greater than mild cognitive impairment (MoCA score < 24 points).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

United States · 1 center
  • Buffalo-Niagara YMCA — Buffalo

Identifiers

NCT: NCT07050589 · 00008757

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗