The development and usability study on intelligent mobile cognitive rehabilitation training system for stroke patients

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000040598

Enrollment

Unknown

Registered

2020-12-03

Start date

2021-01-01

Completion date

Unknown

Last updated

2021-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

stroke

Interventions

Hospital Group:Control group: comprehensive management, including routine care and health management of cognitive impairment in stroke for patients, and health education for family members and caregiv

Community Group:Control group: comprehensive management, including routine care and health management of cognitive impairment in stroke for patients, and health education for family members and caregi

Family Group:Control group: comprehensive management, including routine care and health management of cognitive impairment in stroke for patients, and health education for family members and caregiver

Nursing Home Group:Control group: comprehensive management, including routine care and health management of cognitive impairment in stroke for patients, and health education for family members and car

Eligibility

Sex/Gender

All

Age

45 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Cerebrovascular disease in a stable condition after treatment; 2. aged over 45 years; 3. Education level of elementary school or above; 4. Mild or moderate cognitive impairment (MMSE score 1526, or MMSE score?26 but at the same time MoCA score <27); 5. Cooperation with relevant assessment and training; 6. Standardized drug treatment (including drugs which improve cerebral circulation, antiplatelet, and improve cognitive function) without special adjustment; 7. Ability to provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Consciousness disorder; 2. Severe cognitive dysfunction (MMSE score <15); 3. Severe mental and psychological disorder; 4. Severe aphasia (incoordination because of auditory comprehension); 5. Severe visual, hearing or motor dysfunction; 6. Severe cardiopulmonary dysfunction; 7. Illiterate; 8. Alcohol or drug abuse.

Design outcomes

Primary

Measure	Time frame
Mini-Mental State Examination, MMSE;	—

Secondary

Measure	Time frame
Montreal Cognitive Assessment, MoCA;Prospective and Retrospective Memory Questionnaire, PRMQ;Alzheimer’s Disease-8, AD8;Activity of daily living, ADL;Quality of life index, QLI;Questionnaire for training system;	—

Countries

China

Contacts

Public ContactZhang Hao

Beijing Boai Hospital

zh1665@163.com+86 13701356685

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026