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Transcranial photobiomodulation therapy for behavioral variant frontotemporal dementia

Exploratory study on transcranial photobiomodulation therapy for behavioral variant frontotemporal dementia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081363
Enrollment
Unknown
Registered
2024-02-29
Start date
2024-03-01
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Frontotemporal dementia.

Interventions

NLR treatment group:Carry out 20 minutes of transcranial and transnasal NIR modulation daily, lasting for 4 weeks.
Control group:No stimulation, wear the device for 20 minutes daily, lasting for 4 weeks.

Sponsors

Xuanwu Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Aged 45-70 years old; 2) Have cognitive impairment or behavioral disorders, and meet the diagnostic criteria of "possible bvFTD" in the 2011 International bvFTD Consortium diagnostic criteria; 3) Willing to participate in PET/MRI scans and clinical assessments; 4) Regular use of FTD-related medications, with no medication adjustments in the two months before enrollment and during the enrollment period. 5) Agree to participate and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Accurately differentiate other neurological diseases (such as Alzheimer's disease, Lewy body dementia, Parkinson's disease, cerebrovascular disease, epilepsy, encephalitis, normal pressure hydrocephalus, etc., which may affect cognitive function) based on clinical presentation, MRI, AV45-PET, and FDG-PET; 2) Have systemic diseases that may cause cognitive impairment (such as liver or kidney dysfunction, endocrine disorders, vitamin deficiencies, or tumors), or meet the criteria for DSM-IV depression and schizophrenia patients; 3) History of severe head trauma or prior craniotomy; 4) History of alcohol or substance abuse; 5) Unable to cooperate with imaging examinations, with contraindications for PET imaging, such as patients with pacemakers, implantable cardioverter defibrillators, implanted electronic systems, vascular clips, mechanical heart valves, or cochlear implants. 6) Adjustment of FTD-related medications within the past 2 months, leading to difficulty in determining whether the efficacy is due to medication adjustments or NIR treatment.

Design outcomes

Primary

MeasureTime frame
Neuropsychological assessment scales;

Secondary

MeasureTime frame
PET/MRI scan;

Countries

China

Contacts

Public ContactLiyong Wu

Xuanwu Hospital, Capital Medical University

wmywly@hotmail.com+86 136 8312 0871

Outcome results

None listed

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