UnknownNot Applicable

Subjective Memory Complaints' Cognitive Intervention

10 participantsStarted 2023-02-15

Plain-language summary

This study will be divided into two parts: development of the mobile medical application for older adults with subjective memory decline and the intervention application. Start by developing and optimizing the application based on the rapid prototyping model. Then, in accordance with the framework of designing and evaluating complex intervention measures proposed by the Medical Research Council of the United Kingdom, pre-experiments will be carried out to apply the developed application to the actual intervention process to test the intervention effect, feasibility, and other contents of the application.

Who can participate

Age range

60 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients with subjective memory complaints by SMCQ for 6 months and above. * Individuals age over 60 years (depending on the characteristics of the disease, it can be relaxed to 55 years) are included. * Older adults owning and being able to use smartphones to access the Internet, or whose caregivers can assist in the completion can also be included. * Older adults who voluntary participate in the study and provide informed consent are also included. Exclusion Criteria: * Older adults diagnosed with cognitive or mild cognitive impairment. * Older adults diagnosed with other neurological disorders ( cerebrovascular disease, encephalitis, brain tumor, brain trauma, epilepsy, Parkinson 's disease, depression, mania, etc. ), metabolic diseases ( anemia, thyroid dysfunction, folic acid and vitamin B12 deficiency, etc. ), carbon monoxide poisoning and cognitive decline caused by general anesthesia * Older adults with serious medical and surgical diseases who cannot complete the experiment are also excluded.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Subjective Memory Complaint (SMC)

Timeframe: Change from Baseline Subjective Memory Complaint at 1 month

Cognitive Function

Timeframe: Change from Baseline Cognitive function at 1 month

Memory

Timeframe: Change from Baseline Memory at 1 month

The Quality of Life Rating Scale (SF-12)

Timeframe: Change from Baseline Quality of Life at 1 month

Trial details

NCT IDNCT05720585

SponsorHongli Chen

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-06-30

Contact for this trial

Xianwen Li, PhD

86-025-86869557 xwli0201@njmu.edu.cn

View on ClinicalTrials.gov More Subjective Memory Complaint trials