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Recruiting NCT05561205

NCT05561205 rTMS for Apathy Clinical Trial

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Clinical Trial Summary
NCT ID NCT05561205
Status Recruiting
Phase —
Sponsor Sunnybrook Health Sciences Centre
Condition Alzheimer Disease
Study Type INTERVENTIONAL
Enrollment 10 participants
Start Date 2023-02-09
Primary Completion 2026-12-01

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type INTERVENTIONAL
Interventions
rTMSmethylphenidate

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 10 participants in total. It began in 2023-02-09 with a primary completion date of 2026-12-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Apathy is a common, early, and disabling symptom in dementias and mild behavioural impairment such as Alzheimer's disease (AD) and is characterized by lack of interest and enthusiasm. Both repetitive transcranial magnetic stimulation (rTMS), a form of non-invasive brain stimulation, and methylphenidate, a medication, have been shown to improve apathy. This pilot study will investigate rTMS as a treatment for apathy in neurocognitive disorders and mild behavioural impairment in individuals receiving methylphenidate and individuals not receiving medication for apathy.

Eligibility Criteria

Inclusion Criteria: * mild or major neurocognitive disorder OR mild behavioural impairment * Apathy for at least 4 weeks * Stable dose of medication (\>4 weeks) that may affect cognition or behaviour * Care partner who spends at least 10 hours a week with the subject Exclusion Criteria: * Current major depressive episode * Agitation, delusions, hallucination * Medical contraindications to rTMS * Currently taking an amphetamine product * Central nervous system abnormalities, Tourette's syndrome, or motor tics * Current participation in another clinical trial

Frequently Asked Questions

Who can join the NCT05561205 clinical trial?

This trial is open to participants of all sexes, studying Alzheimer Disease. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05561205 currently recruiting?

Yes, NCT05561205 is actively recruiting participants. Visit ClinicalTrials.gov or contact Sunnybrook Health Sciences Centre to inquire about joining.

Where is the NCT05561205 trial being conducted?

This trial is being conducted at Toronto, Canada.

Who is sponsoring the NCT05561205 clinical trial?

NCT05561205 is sponsored by Sunnybrook Health Sciences Centre. The trial plans to enroll 10 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology