跳至主要内容
临床试验/NCT06648343
NCT06648343已完成不适用

Effect of Cognitive and Physical Function Training in the Elderly

Bundang CHA Hospital1 个研究点 分布在 1 个国家目标入组 27 人开始时间: 2020年9月25日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
27
试验地点
1
主要终点
K-MMSE (Korean Mini-Mental Status Examination)

研究概览

简要总结

This is a single-arm intervention study aimed at investigating whether a 4-week program of daily cognitive and physical activities, lasting 2-3 hours per day, produces significant changes in functional levels in healthy adults aged 65 and older.

详细描述

Purpose of the Clinical Study The aim of this clinical study is to evaluate the effects of cognitive and physical function training in elderly individuals (including those with subjective cognitive decline) to aid in the development of preventive and therapeutic methods for dementia.

Study Participants -Number of Participants and Basis This is a pilot study, and no formal sample size calculation was performed. The study will include 30 participants.

Clinical Study Procedure and Assessment Visit 1 (Screening) During the screening visit, the researcher will select participants based on the inclusion/exclusion criteria. All study-related assessments will take place after obtaining consent. However, if any assessments were performed within 7 days of the screening visit, those results may be used instead. The following activities will be conducted:

Visit 2 (Baseline Assessment) Baseline assessments will be conducted, and Visit 1 and Visit 2 can be performed on the same day. The following activities will be conducted:

After the baseline assessment, participants will receive self-training materials for a 4-week program, jointly developed by EBS (Korea Educational Broadcasting System) and Bundang CHA Hospital. The cognitive and physical function training program will be conducted five times a week for 40 minutes per session. The effectiveness will be evaluated through baseline assessments, and post-training assessments will be conducted after 4 weeks to analyze the results.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • •Adults aged 65 years or older.
  • •Individuals capable of independent daily living (including mobility).
  • •Individuals who fully understand the study and voluntarily agree to participate, providing written consent.

排除标准

  • •MMSE score less than 20 (19 or below will be excluded).
  • •Individuals with neurological conditions such as stroke, brain tumor, cerebral palsy, dementia, or Parkinson's disease.
  • •Individuals with serious medical conditions (cardiovascular, gastrointestinal, respiratory, endocrine, etc.) that compromise their general health.
  • •Participants currently involved in other clinical studies or who participated in another clinical trial within the past 30 days.
  • •Any other conditions deemed inappropriate for study participation by the researcher.

研究组 & 干预措施

Intervention

Experimental

Intensive cognitive and physical training

干预措施: Intensive cognitive and physical training (Other)

结局指标

主要结局

K-MMSE (Korean Mini-Mental Status Examination)

时间窗: 4 weeks

The Mini-Mental State Examination (MMSE) is a widely used screening tool for assessing cognitive function. It is designed to evaluate different cognitive abilities, including memory, attention, language, orientation, and visuospatial skills. The MMSE consists of a series of questions and tasks, with a maximum score of 30 points.

次要结局

  • RBANS (Repeatable Battery for the Assessment of Neuropsychological Status)(4 weeks)
  • K-MBI (Korean Version of the Modified Barthel Index)(4 weeks)
  • BBS (Berg Balance Scale)(4 weeks)

研究者

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

MinYoung Kim, MD, PhD

Prof

Bundang CHA Hospital

研究点 (1)

Loading locations...

相似试验