Subjective Memory Complaints' Cognitive Intervention

NCT ID: NCT05720585

Last Updated: 2023-02-09

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-02-15
• Study Completion Date: 2023-12-31

Brief 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.

Conditions

Subjective Memory Complaint

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Intervention group

Group Type: EXPERIMENTAL

Intervention of mobile health application

Intervention Type: OTHER

According to the contents of the Subjective Memory Complaint (SMC) application intervention program for the older adults previously formulated, the intervention time and the frequency (30min / time, once a week) of each training module and other contents were determined. The application will be implemented and lasted for a total of 1 month.

Interventions

Intervention of mobile health application

According to the contents of the Subjective Memory Complaint (SMC) application intervention program for the older adults previously formulated, the intervention time and the frequency (30min / time, once a week) of each training module and other contents were determined. The application will be implemented and lasted for a total of 1 month.

Intervention Type: OTHER

Eligibility Criteria

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.

• Minimum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Hongli Chen

OTHER

Sponsor Role: lead

Responsible Party

Hongli Chen

Research assistant

Responsibility Role: SPONSOR_INVESTIGATOR

Central Contacts

Xianwen Li, PhD

Role: CONTACT

xwli0201@njmu.edu.cn

86-025-86869557

Hongli Chen, Master

Role: CONTACT

chenhl@njmu.edu.cn

86-13260702093

Other Identifiers

NMU-IRB-(2019)437

Identifier Type: -

Identifier Source: org_study_id