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Clinical Trials/NCT06371053
NCT06371053
Not yet recruiting
Not Applicable

The Effect of Community Intervention on Different Degrees of Dementia: A Randomized Controlled Study

Babujinaya Cela0 sites200 target enrollmentApril 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Alzheimer Disease
Sponsor
Babujinaya Cela
Enrollment
200
Primary Endpoint
Mini-Mental State Examination
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

The goal of this clinical trial is to explore the impact of Community Intervention on Dementia and Activities of Daily Living in community-dwelling elderly individuals (≥60 year old) with Alzheimer's disease. It primarily aims to address: the effects of Community Intervention on Dementia and Activities of Daily Living in community-dwelling elderly individuals with Alzheimer's disease in different degrees. All participants are required to undergo a continuous 2-week (14 days) Community Intervention, with weekends off and training conducted only on weekdays. The training will be conducted two sessions per day, lasting 30 minutes each.

Detailed Description

Regular exercise can increase brain function, improve memory, speed up cognitive processes, and fight off diseases like Alzheimer ' s and dementia. The goal of this clinical trial is to explore the impact of Community Intervention on Dementia and Activities of Daily Living in community-dwelling elderly individuals (≥60 year old) with Alzheimer's disease. It primarily aims to address: the effects of Community Intervention on Dementia and Activities of Daily Living in community-dwelling elderly individuals with Alzheimer's disease in different degrees. All participants are required to undergo a continuous 2-week (14 days) Community Intervention, with weekends off and training conducted only on weekdays. The training will be conducted two sessions per day, lasting 30 minutes each.

Registry
clinicaltrials.gov
Start Date
April 2024
End Date
May 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Babujinaya Cela
Responsible Party
Sponsor Investigator
Principal Investigator

Babujinaya Cela

Research Director

Buraidah Central Hospital

Eligibility Criteria

Inclusion Criteria

  • Age over 60 years old.
  • No hospitalization within the past six months.
  • Alzheimer's disease
  • The elderly people who voluntarily participate and agree to adhere until the end of the study.

Exclusion Criteria

  • Complicated with severe liver and kidney failure, tumors, or hematological disorders.
  • Physical disability.
  • Difficulty in mobility.
  • Simultaneously receiving other therapies that might influence this study.

Outcomes

Primary Outcomes

Mini-Mental State Examination

Time Frame: day 1 and day 14

The Mini-Mental State Examination (MMSE) is a widely used tool for assessing cognitive function, particularly in the elderly population. It evaluates various cognitive domains such as orientation, memory, attention, calculation, and language. The test consists of a series of questions and tasks, including asking the individual to state the current date, recall a list of words, perform simple calculations, and follow verbal commands. Each correct response earns a certain number of points, and the total score ranges from 0 to 30, with higher scores indicating better cognitive function.

Secondary Outcomes

  • Barthel Index(day 1 and day 14)
  • Functional near-infrared spectroscopy(day 1 and day 14)

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