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Effects of Transcranial Direct Current Stimulation Over the Supplementary Motor Area Combined With Nordic Walking on Gait and Balance in Parkinson's Disease

Status: Recruiting
Location: See location...
Intervention Type: Behavioral, Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Parkinson's disease can cause slow or unsteady walking and balance problems that raise the risk of falls. This study will test whether adding a gentle, non-invasive brain stimulation called transcranial direct current stimulation (tDCS) during a supervised Nordic Walking program improves mobility in people with Parkinson's disease. Participants will be randomly assigned to receive either active tDCS or an inactive (sham) procedure that feels the same but does not deliver current, while both groups complete the same supervised walking program. Sessions occur three times per week for four weeks. We will measure walking speed with a 10-Meter Walk Test as the main outcome, and also evaluate balance, motor symptoms, quality of life, and any side effects. We expect that tDCS given during the walking sessions will help people walk faster and feel steadier compared with the walking program alone.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Maximum Age: 75
Healthy Volunteers: f
View:

• Idiopathic Parkinson's disease (e.g., UK Brain Bank criteria)

• Hoehn \& Yahr stage II-IV (on medication)

• Stable antiparkinsonian medication for ≥4 weeks before enrollment

• Slowed gait phenotype (e.g., ≥6 seconds on 10-Meter Walk at preferred speed)

• Able to ambulate at least 10 meters with or without a cane/poles (no hands-on assistance from a therapist)

• Able to follow simple commands; provides written informed consent (MMSE ≥24 or equivalent cognitive screening)

• Willing to maintain stable PD medication and usual care during the 4-week intervention, unless medically required

Locations
Other Locations
Brazil
UEAFTO - Unidade de Fisioterapia e Terapia Ocupacional
RECRUITING
Belém
Time Frame
Start Date: 2025-06-09
Estimated Completion Date: 2026-03
Participants
Target number of participants: 40
Treatments
Experimental: Active tDCS over SMA + standardized Nordic Walking
Participants receive anodal tDCS over the supplementary motor area (SMA) delivered concurrently with a standardized 30-minute Nordic Walking (NW) session, 3×/week for 4 weeks (12 sessions). tDCS: 2.0 mA, 20 min, saline-soaked sponge electrodes (5×7 cm), anode over midline SMA (FCz), cathode supraorbital contralateral; 30-s ramp-in/out. NW protocol identical across both arms (warm-up, technique practice with poles, continuous walking at moderate effort, cool-down).
Sham_comparator: Sham tDCS + standardized Nordic Walking
Participants undergo the same NW protocol (30 min) on the same schedule (3×/week for 4 weeks; 12 sessions) while receiving sham tDCS with brief ramp-in/out to mimic sensations and no sustained current; electrodes and device indicators match the active condition.
Related Therapeutic Areas
Sponsors
Leads: Universidade Metodista de Piracicaba

This content was sourced from clinicaltrials.gov