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临床试验/NCT07050589
NCT07050589进行中(未招募)不适用

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

State University of New York at Buffalo2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年10月15日最近更新:
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
80
试验地点
2
主要终点
Cognitive Function: Attention

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
60 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • > = 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

排除标准

  • 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).

研究组 & 干预措施

Program

Experimental

Program participants will receive the recreation-based program.

干预措施: Exercise and art (Behavioral)

Control

No Intervention

Control participants will receive no recreation-based program.

结局指标

主要结局

Cognitive Function: Attention

时间窗: From enrollment to week 8 and then week 16

Change in performance on the Trail-Making Test

次要结局

  • Balance(From enrollment to week 8 and then week 16)
  • Dual-Task Performance(From enrollment to week 8 and then week 16)
  • Cognitive Function: Interference Inhibition(baseline to week 8, through week 16)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nikhil Satchidanand

Assistant Professor of Internal Medicine

State University of New York at Buffalo

研究点 (2)

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