Exploratory randomized controlled study on a new model of fine motor cognitive collaborative intervention based on virtual reality technology in elderly individuals with cognitive impairment

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400093152

Enrollment

Unknown

Registered

2024-11-29

Start date

2024-12-01

Completion date

Unknown

Last updated

2024-12-02

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

Conditions

Cognitive impairment

Interventions

Autonomous exercise group:All participants will receive health education on the prevention and treatment of cognitive impairment. Participants in the autonomous exercise group can decide their own exe

Traditional fine motor cognitive collaborative training group:The traditional fine motor cognitive collaborative training group received finger exercise training as required, along with cognitive func

New Precision Motor Cognitive Collaborative Training Group:The new type of fine motor cognitive collaborative training group, with the assistance of staff, wears portable VR headsets and inertial moti

Eligibility

Sex/Gender

All

Age

60 Years to 74 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 60-74 years old; 2.Meets the diagnostic criteria for MCI: patients or informants report or experienced clinicians discover cognitive impairment; Objective evidence of impairment in one or more cognitive domains (from cognitive scale testing); Complex instrumental daily skills may have slight impairments, but maintain independent daily living abilities; Has not yet reached the diagnosis of dementia; 3.Chronic diseases and stable functional status.

Exclusion criteria

Exclusion criteria: 1.Diagnosed with vascular dementia and Lewy body dementia; 2.Individuals with residual upper limb movement disorders due to previous cerebrovascular disease; 3.Diagnosed with Parkinson's disease and Parkinson's syndrome; 4.Individuals with osteoarthritis that affects their motor function; 5.Those who have suffered fractures within 12 months; 6.Extremely limited visual and auditory abilities affecting normal communication; 7.Diagnosed with severe dementia; 8.Patients with severe illnesses or expected survival of less than 1 year or unstable functional status; 9. Recently received other cognitive rehabilitation interventions; 10.I am currently participating in other clinical studies.

Design outcomes

Primary

Measure	Time frame
Assessment of global cognitive function;Assessment of independent cognitive dimensions;	—

Secondary

Measure	Time frame
Assessment of Hand Fine Motor Function;Assessment of Daily Living Ability and Physical Function;Emotional and psychological assessment;Plasma biomarker detection;	—

Countries

China

Contacts

Public ContactYejing Zhao

Beijing Hospital

yejing27@126.com+86 151 0101 2590

Outcome results

None listed

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