Dual-Task Training Effects on Older Adults' Cognitive and Physical Health
The study aims to evaluate how dual-task training can improve cognitive and physical health in older adults by measuring changes in manual dexterity, social integration, cognitive processing, attention, daily living activities, and mobility.
the additional dual-task training group (ADT)
+ the incorporated dual-task training group (IDT)
Supportive Care Study
Summary
Study start date: April 1, 2020
Actual date on which the first participant was enrolled.This study is designed to explore the effectiveness of two different types of dual-task training programs on various aspects of health in older adults living in the community. The focus is on comparing the effects of an Incorporated Dual-Task (IDT) program with an Additional Dual-Task (ADT) program. The goal is to see how these programs impact cognitive functions, physical abilities, daily living activities, and overall quality of life. This research is important because improving these areas can help older adults maintain independence and enhance their well-being. Participants in the study engage in activities designed to test manual dexterity, social integration, information processing speed, attention, and memory. Tests like the Box and Block Test, Community Integration Questionnaire, and Digit Symbol Substitution Test are used to measure these outcomes. Additionally, participants perform tasks to evaluate their ability to live independently, such as using the Lawton Instrumental Activities of Daily Living scale. The study also assesses cognitive functions using the Montreal Cognitive Assessment and other tests. These assessments help determine the benefits and effectiveness of the dual-task training programs in improving the participants' capabilities and quality of life.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.164 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 60 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Inclusion Criteria: * Age ≥ 60 years * Able to follow instructions (Mini-Mental State Examination score ≥ 20) * Montreal Cognitive Assessment (MoCA) score \> 20 * No difficulty performing basic activities of daily living * No diagnosis of dementia confirmed by a neurologist Exclusion Criteria: * Self-reported diagnosis of neurological disorders * Unstable medical conditions (e.g., recent myocardial infarction, heart failure, recent heart surgery, or severe asthma)
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location