Skip to content

Evaluation of Artificial Intelligence-Based Rivastigmine on Gait Improvement in Patients with Cognitive Impairment and Correlation Analysis

Evaluation of Artificial Intelligence-Based Rivastigmine on Gait Improvement in Patients with Cognitive Impairment and Correlation Analysis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113570
Enrollment
Unknown
Registered
2025-12-01
Start date
2026-01-01
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Cognitive disorder

Interventions

Treatment group:For the first 4 weeks, 4.6 mg. If no adverse reactions occur during the first 4 weeks of treatment, it is considered that the patient can tolerate it. If tolerated, 9.5 mg can be admin
if not tolerated, maintain at 4.6 mg.
Control group:Cholinesterase inhibitors such as rivastigmine patches have not been used.

Sponsors

Hangzhou Normal University Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=40 years old; 2. Meet the corresponding diagnostic criteria for cognitive impairment and be evaluated by the ADAS-cog scale; 3. Have the ability to walk independently and be compatible with wearable devices Gait assessment of the equipment; 4. The patient or their family member signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Currently using cholinesterase inhibitors or having adjusted to other cognitive-improving drugs within the past three months; 2. Combined with severe mental disorders or serious internal diseases, unable to cooperate with the assessment; 3. Known allergy to Risamin/carbapatine, other carbamate derivatives or excipients.

Design outcomes

Primary

MeasureTime frame
ADAS-cog;Gait;

Countries

China

Contacts

Public ContactDanning Lou

Hangzhou Normal University Affiliated Hospital

candy2379363@163.com+86 136 1655 7055

Outcome results

None listed

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