NCT07356687Recruiting
Effects of rTMS Combined With Dual-Task Gait Training on Walking and Cognition After Stroke
Effects of Dorsolateral Prefrontal Cortex rTMS Primed Dual-Task Gait Training on Walking and Cognitive Outcomes After Stroke: A Randomized Sham-Controlled Trial
Source: ClinicalTrials.gov · Last updated 10 Jul 2026
Brief summary (registry, in English)
This randomized, double-blind, placebo-controlled trial will investigate whether repetitive transcranial magnetic stimulation (rTMS) applied to the dorsolateral prefrontal cortex (DLPFC) can enhance the effects of dual-task gait training in people with chronic stroke. Participants will be randomly allocated to receive either active rTMS or sham rTMS immediately before the same standardized dual-task gait training program. The intervention includes 12 sessions over 3 weeks. Outcomes will be assessed at baseline, immediately after training, and at 4-week follow-up. Co-primary outcomes are dual-task mobility and cognitive performance during walking, quantified using dual-task cost (DTC) for gait speed and cognitive-task performance during dual-task walking (e.g., Serial 7s; Shopping List Recall). Secondary outcomes include balance/mobility, community participation, mood/sleep measures, and fall incidence. To explore mechanisms, prefrontal cortex activity during single- and dual-task walking will be recorded using functional near-infrared spectroscopy (fNIRS), and mediation analyses will examine whether changes in PFC activity explain intervention effects.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 184 (estimated)
- First submitted
- 30 Dec 2025
- Start date
- 21 Jan 2026
- Primary completion date
- Jun 2028
- Lead sponsor
- The Hong Kong Polytechnic University
- Diseases
- Stroke
- NCT number
- NCT07356687
What you commit to
- Study type: Interventional
- Planned participants: 184
- From 21 Jan 2026 to the primary completion date, Jun 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Concurrent formal rehabilitation elsewhere
Other illness
- Other neurological disorders
- TMS contraindications (e.g., pacemaker, intracranial metal, seizure history, pregnancy)
- Contraindications to exercise (e.g., unstable angina)
- Pain/illness limiting performance
Other
- Cerebellar/brainstem injury
- Severe aphasia (NIHSS item 9 ≥ 2)
- RMT cannot be determined
- Fails TMS safety screening
Who the study is looking for
- Unilateral ischemic or hemorrhagic hemispheric stroke
- Age ≥ 50 years
- -≥ 6 months post-stroke
- Medically stable
- Able to walk independently ≥ 1 minute (assistive device allowed)
- Able to follow commands
- mRS 1-3
- MoCA ≥ 22
Age in the registry: 50 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| The Hong Kong Polytechnic University Coordinator of this site? Confirm its status | Hong Kong | Hong Kong SAR China | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.