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Flexible wearable transcranial magnetic stimulation for cognitive frailty: A randomized double-blinded controlled study

Flexible wearable brain-computer interactive digital technology, for the screening, diagnosis, and intervention of frailty phenotypes - Flexible wearable transcranial magnetic stimulation for cognitive frailty: A randomized double-blinded controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085019
Enrollment
Unknown
Registered
2024-05-29
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-06-03

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

Conditions

cognitive frailty

Interventions

cognitive frailty:transcranial magnetic stimulation
cognitive frailty with subjective tinnitus:transcranial magnetic stimulation
cognitive frailty:sham transcranial magnetic stimulation
cognitive frailty with subjective tinnitus:sham transcranial magnetic stimulation

Sponsors

Huadong hospital, Shanghai medical college, Fudan university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Aged 60 years and older, and no more than 90 years old community dwelling adults. 2. Old adults with cognitive frailty, cognitive frailty combined with subjective tinnitus. 3. Idividuals can comply with the test protocol and with informed consent form signed by family members or guardians.

Exclusion criteria

Exclusion criteria: 1. With serious neurological/mental diseases, dementia, severe depression and anxiety; Autoimmune diseases, vital organ failure, terminal disease. 2. Medicine have significant effect on cognition 3.Disability (dependence, profound hearing loss, blindness) 4. Actue inflammational diseases, brain trauma, and stroke 5. scarce of informed consent 6. Scarce of basic personal information 7. Can not conduct some important tests 8. Serious alcohol or drug abuse 9. Participate other clinical study simultaneously 10. Other issues that researchers believe that those who cannot be included in the study

Design outcomes

Primary

MeasureTime frame
cognitive performance;tinnitus;cognitive frailty;psychological performance ;hearing function;

Secondary

MeasureTime frame
quality of life;Activities of Daily Living;Instrumental Activities of Daily Living (IADL);3-T Magnetic Resonance Imaging (MRI) and functional MRI;neurotransmitter;adverse event;

Countries

China

Contacts

Public ContactZhijun Bao

Huadong hospital, fudan university

Zhijunbao@fudan.edu.cn+86 21 6248 3180

Outcome results

None listed

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