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NOT YET RECRUITING
NCT06581458
NA

Home Transcranial Direct-Current Stimulation for Motoric Cognitive Risk Syndrome

Sponsor: Tel-Aviv Sourasky Medical Center

View on ClinicalTrials.gov

Summary

1. To examine the effect of a two-week tDCS intervention of 3 months of continued tDCS intervention versus 3 months of receiving a placebo treatment (dummy). On the costs of performing an action task (dual task cost) walking speed, cognitive measures and motor function. 2. To examine whether the effects of tDCS build up over time by creating a delayed start mechanism in the intervention (delayed-start design) 3. Examining mechanical and neuroplastic effects of tDCS intervention 4. To examine the response to tDCS over time

Key Details

Gender

All

Age Range

65 Years - 90 Years

Study Type

INTERVENTIONAL

Enrollment

64

Start Date

2024-09

Completion Date

2026-09

Last Updated

2024-09-03

Healthy Volunteers

No

Interventions

DRUG

tDCS

The immediate intervention group will continue to receive five tDCS treatments per week for 6 months. The late intervention group will receive five sham treatments per week for 3 months and then begin receiving five weekly tDCS treatments for an additional 3 months.