Last updated: March 19, 2021
Sponsor: University of Manitoba
Overall Status: Active - Recruiting
Phase
N/A
Condition
Communication Disorders
Frontotemporal Dementia
Dementia
Treatment
N/AClinical Study ID
NCT04193267
HS23339 (B2019:108)
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Diagnosis of PPA-L (confirmed by a neurologist or neuropsychiatrist who has observedthe patient for at least one year);
- Mild to moderate language impairment as assessed by the Druks and Masterson NamingTask;
- Native English speaker.
Exclusion
Exclusion Criteria:
- Cerebrovascular disorders, hydrocephalus or intra-cranial mass, documented by MRI;
- History of traumatic brain injury, seizures, or another neurological disease;
- Significant medical problems (e.g. poorly controlled diabetes or hypertension orcancer within the past 5 years);
- Major depressive disorder, bipolar disorder, schizophrenia, substance use disorder ormental retardation according to the criteria of the DSM-IV;
- Any contraindication for rTMS (e.g., implanted metal devices; cardiac pacemaker orpacemaker wires; neurostimulators; implanted pumps, metal in the body [rods, plates,screws, shrapnel, dentures, IUD] or metallic particles in the body, surgical clips inthe head, previous neurosurgery, cochlear implants, prosthetic heart valves);
- Currently pregnant or breastfeeding.
Study Design
Total Participants: 10
Study Start date:
June 01, 2020
Estimated Completion Date:
December 31, 2022
Study Description
Connect with a study center
St. Boniface Hospital
Winnipeg, Manitoba R2H2A6
CanadaActive - Recruiting
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