Computer-based Memory Strategy Training for Older Adults
This clinical trial is evaluating the acceptability of a computer-based memory strategy training for older adults, using a structured questionnaire to assess their perception of effectiveness, relevance, convenience, and clarity.
E-MinD Life Semantic
+ Cognitive stimulation
Mental Disorders+1
+ Cognition Disorders
+ Neurocognitive Disorders
Treatment Study
Summary
Study start date: February 10, 2025
Actual date on which the first participant was enrolled.This study looks at how a computer-based program called E-MinD Life (Semantic) can help improve daily life skills in older adults. It focuses on three groups in Hong Kong: healthy older adults, those with memory complaints, and those with mild cognitive problems like Mild Cognitive Impairment (MCI) or mild dementia. The goal is to see if this program can make everyday tasks easier for these groups. This research is important because it could provide new ways to support individuals with memory concerns or early stages of dementia, helping them maintain their independence and quality of life. Participants in this study will be randomly assigned to different groups to test the effectiveness of the program. They will use the computer-based training, which is designed to work on memory and cognitive skills. Researchers will measure the impact of this program by recording changes in participants' cognitive scores, using tools like the Montreal Cognitive Assessment. Family members or caregivers are also involved, as their observations can provide additional insights into the participants' progress. The study aims to gather information on how practical and beneficial this training is for improving day-to-day functioning in older adults.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.60 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment 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 65 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.Conditions
Pathology
Criteria
Inclusion Criteria: Group 1: healthy older adults aged 65 years or above Group 2: older adults aged 65 years or above with memory complaints Group 3: older adults aged 65 or above with mild cognitive impairment Exclusion Criteria (for all groups 1, 2 and 3) \- have depression and other clinical conditions that may affect their cognition.
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
Active ComparatorStudy Objectives
Primary Objectives
Secondary 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
The Hong Kong Polytechnic University
Hong Kong, Hong KongOpen The Hong Kong Polytechnic University in Google Maps