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Artificial intelligence (AI)-assisted systematic, standardized and hierarchical physical stimulus load intensity detection system construction clinical research

Artificial intelligence (AI)-assisted systematic, standardized and hierarchical physical stimulus load intensity detection system construction clinical research

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093566
Enrollment
Unknown
Registered
2024-12-09
Start date
2025-01-01
Completion date
Unknown
Last updated
2024-12-16

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

Conditions

Healthy elderly

Interventions

Transcranial direct current stimulation group:Scheme 1: Set the stimulation intensity of the transcranial direct current stimulation device to 1mA and conduct continuous treatment for 10 minutes. Sche
Transcranial magnetic stimulation group:Scheme 1: Set the transcranial magnetic stimulation device to a frequency of 10 Hz, RMT 90%, 1200 pulses, 20 minutes, stimulate for 1 second and rest for 9 seco

Sponsors

Beijing Rehabilitation Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age between 40 and 80 years old; 2. No severe neurological diseases, such as severe cerebral infarction (modified Rankin scale score >= 3 points), sequelae of cerebral hemorrhage affecting limb motor function (lower limb motor function evaluated by Fugl-Meyer = 4 stages), etc; 3. No severe cardiovascular diseases, such as severe heart failure (New York Heart Association cardiac function classification grade III-IV), unstable angina pectoris (Canadian Cardiovascular Society angina pectoris classification grade III-IV), etc; 4. No musculoskeletal system diseases, such as unhealed fractures, severe joint deformities (joint range of motion reduction > 50%), etc; 5. No open wounds, skin infections, rashes, etc. on the limbs that affect the adhesion of electrode patches and the implementation of electrical stimulation; 6. Able to understand and willing to abide by all procedures stipulated in the protocol; 7. The subject himself or his legal representative signs the Informed Consent Form.

Exclusion criteria

Exclusion criteria: 1. Unable to understand words or there are any factors that may hinder the completion of neuropsychological assessment; 2. Have a history of alcohol or drug abuse; 3. Be using drugs that may affect this study, including sedatives, anti-anxiety drugs, hypnotics, nootropic drugs and cholinergic drugs, etc; 4. There is a sharp change in body function within 30 days; 5. Currently being treated with force, sound, light, magnetism, electricity and cannot stop; 6. Have a cochlear implant, a pacemaker, an implantable device (i.e., deep brain stimulation, or metal in the brain).

Design outcomes

Primary

MeasureTime frame
Average power of alpha wave;Average power of theta waves;Average power of beta waves;?-? phase-amplitude coupling value;Task-related ERP;

Secondary

MeasureTime frame
comfort rating;fatigue score;tolerance score;blood pressure;Heart rate variability;respiratory rate;Muscle oxygen saturation;blood oxygenation index;Maximum voluntary contraction force value of muscle;Mean difference of electromyogram amplitude;Muscle hardness value;muscle tone magnitude;Peak difference of electromyogram amplitude;muscle power;

Countries

China

Contacts

Public ContactQie Shuyan

Beijing Rehabilitation Hospital, Capital Medical University

shuyanpb@163.com+86 156 2499 4391

Outcome results

None listed

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