Actively Recruiting
Investigating Neurophysiological Effects of Transcranial Direct Current Stimulation Combined with Action Observation Therapy on Hand Muscle Neuroplasticity in Chronic Stroke
Led by Universiti Malaysia Sabah · Updated on 2026-05-12
60
Participants Needed
2
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating how the combined use of transcranial direct current stimulation (tDCS) and action observation therapy (AOT) may help improve hand motor recovery in people who have had a stroke. This study focuses on understanding the brain mechanisms involved when these two therapies are used together, as both have shown promise separately for stroke rehabilitation. The trial is a randomised controlled study involving 60 participants with chronic stroke from Sabah, Malaysia. Participants will be randomly assigned to one of three groups: one group will receive active anodal tDCS with AOT, another will receive sham (placebo) tDCS with AOT, and the third will receive active tDCS alone. The treatment involves 10 sessions over two weeks in a clinic, where tDCS is applied for 20 minutes and AOT or control videos are watched for 30 minutes during each session. After the clinic phase, participants will continue home-based AOT or control video practice for 30 minutes a day, five days a week, for eight weeks. During the 10-week study, participants will attend outpatient sessions monitored by a physiotherapist to ensure proper participation and will be assessed at baseline, after two weeks, and at the end of 10 weeks. Researchers will measure changes in brain motor pathways using motor evoked potentials (MEPs) and evaluate clinical hand function using standard tests. Participant activity levels will be tracked using a perceived exertion scale, and safety and compliance will be closely monitored throughout the study.
CONDITIONS
Brief Title
Brain Stimulation Combined With Watching Hand Movements to Improve Hand Recovery in Chronic Stroke
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 59 years
- Single episode of unilateral stroke with hand muscle weakness 6 to 24 months post-stroke
- Upper limb spasticity grade two or less on Modified Ashworth Scale
You will not qualify if you...
- Diagnosed with posterior circulation infarction
- Unable to follow commands due to poor cognitive function
- Presence of unilateral neglect
- Presence of homonymous hemianopia
- Other neurological disorders causing poor hand function
- Hand muscle strength grade four or five
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 10 weeks
Participants attend outpatient clinic sessions for transcranial direct current stimulation (tDCS) combined with action observation therapy (AOT), sham tDCS with AOT, or tDCS with landscape video watching. This is followed by home-based AOT or video watching sessions.
5 visits per week for 2 consecutive weeks at outpatient clinic; then daily home sessions 5 days per week for 8 consecutive weeks
Trial Site Locations
Total: 2 locations
1
Hospital Universiti Malaysia Sabah (HUMS)
Kota Kinabalu, Sabah, Malaysia, 88400
Actively Recruiting
2
Queen Elizabeth Hospital
Kota Kinabalu, Sabah, Malaysia, 88586
Enrolling by Invitation
Research Team
C
Candace Goh Xiao Huey, Msc.
F
Fatimah Ahmedy, MRehabMed
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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