Skip to content

A trial on the therapeutic effect of repetitive transcranial magnetic stimulation (rTMS) as add-on treatment in mild-moderate dementia patients

Effect of Repetitive Transcranial Stimulation (rTMS) as add-on treatment in mild-moderate dementia: a Randomised Controlled Trial Comparing Treatment as Usual vs Treatment as Usual with rTMS - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106757
Enrollment
100
Registered
2026-03-23
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: G30- Alzheimers disease

Interventions

Intervention1: rTMS with treatment as usual: rTMS protocol: Target: Left dorsolateral prefrontal cortex (DLPFC) Frequency: 10 Hz Intensity: 110% resting motor threshold Pulses: 2000 per session Sched

Sponsors

Tribeni Bhuyan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Diagnosis of Alzheimer type of Dementia as per DSM-5 and NIA-AA criteria 2. Stable on medications Donepezil and or Memantine 10mg for at least 3 months 3. with Mini Mental State Examination score between 15 to 26

Exclusion criteria

Exclusion criteria: 1. Other neurological disorders affecting cognition 2. History of epilepsy or significant head injury 3. Implanted metallic devices or pacemakers 4. Other psychiatric illness including substance use disorder 5. Contraindications to MRI or rTMS

Design outcomes

Primary

MeasureTime frame
Change in cognition assessed by MoCA (Montreal Cognitive Assessment), Addenbrook Cognitive Examination (ACE) and Mini Mental State Examination (MMSE) scores from baselineTimepoint: 1 month, 3 months and 6 months

Secondary

MeasureTime frame
Assessment of functional status using the Bristol Activities of Daily Living (ADL)Timepoint: 1 month, 3 months, 6 months;Assessment of behavioural and psychological symptoms of dementia using the Neuropsychiatric Inventory (NPI)Timepoint: 1 month, 3 months, 6 months

Countries

India

Contacts

Public ContactTribeni Bhuyan

AIIMS Guwahati

tribenibhuyan@aiimsguwahati.ac.in9435697956

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026