跳至主要内容
临床试验/NCT06849557
NCT06849557招募中不适用

Effectiveness of Chair-bound Exergaming on Physical and Cognitive Functions in Pre-frail/ Frail Older Adults in Nursing Home: A Pilot Randomized Controlled Trial

Hong Kong Metropolitan University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年4月7日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
1
主要终点
enjoyment

研究概览

简要总结

This pilot randomized controlled trial is designed to investigate the effectiveness of chair-bound exergaming on improving physical and cognitive function in pre-frail/ frail nursing home residents

详细描述

Objective To explore the effects of the chair-bound exergaming on the enjoyment of physical activity in in pre-frail/ frail nursing home residents.

To evaluate the effects of the chair-bound exergaming in improving physical and cognitive function in pre-frail/ frail nursing home residents.

Research plan and methodology Thirty nursing home residents will be recruited from the nursing homes.

All the eligible participant will be randomly allocated to either one of the following 2 groups (i) Exergaming (intervention group), or (ii) wait list control.

  1. Intervention group (exergaming group, ERG) Those allocated to the ERG will receive supervised chair-bound exercise programme for 12 weeks.
  2. Control group (wait list control, CG) Those allocated to the CG will receive supervised chair-bound exercise programme for 12 weeks after post-assessment.

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
Double (Participant, Investigator)

入排标准

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

入选标准

  • •older adults aged 60 years or older living in the nursing homes;
  • •pre-frail or frail according to the Fried Frailty Phenotypes;
  • •ability to understand and execute instructions; and
  • •ability to sit unassisted on a chair or in a wheelchair.

排除标准

  • •no controlled medical diagnosed of severe cardiometabolic, respiratory and musculoskeletal disorders;
  • •any conditions that hinder the participation of intervention and assessment; and
  • •being involved in any other clinical trials.

研究组 & 干预措施

Wait-list Control

No Intervention

Wait list control, after post-test, 12 week supervised exercise intervention

Exergaming

Experimental

12-week exergaming intervention

干预措施: Exergaming (Behavioral)

结局指标

主要结局

enjoyment

时间窗: T2: immediately (1 week) after intervention

enjoyment of physical activity measured by Physical Activity Enjoyment Scale (PACES)

upper extremity endurance

时间窗: T2: immediately (1 week) after intervention

upper extremity endurance measured by arm curl test

upper extremity endurance

时间窗: T0: baseline

upper extremity endurance measured by arm curl test

upper extremity endurance

时间窗: T1: 6 week

upper extremity endurance measured by arm curl test

enjoyment

时间窗: T0: baseline

enjoyment of physical activity measured by Physical Activity Enjoyment Scale (PACES)

enjoyment

时间窗: T1: 6 week

enjoyment of physical activity measured by Physical Activity Enjoyment Scale (PACES)

次要结局

  • upper extremity strength(T2: immediately (1 week) after intervention)
  • cognitive function(T2: immediately (1 week) after intervention)
  • lung capacity(T2: immediately (1 week) after intervention)
  • sitting balance(T2: immediately (1 week) after intervention)
  • feasibility, acceptability and appropriateness of intervention(T2: immediately (1 week) after intervention)
  • mental health(T2: immediately (1 week) after intervention)
  • upper extremity strength(T0: baseline)
  • upper extremity strength(T1: 6 week)
  • lung capacity(T0: baseline)
  • lung capacity(T1: 6 week)
  • sitting balance(T0: baseline)
  • sitting balance(T1: 6 week)
  • mental health(T0: baseline)
  • mental health(T1: 6 week)
  • cognitive function(T0: baseline)
  • cognitive function(T1: 6 week)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验