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Clinical Trials/NCT04051671
NCT04051671CompletedNot Applicable

Effects of Dual-transcranial Direct Current Stimulation During Physical Therapy in Sub-acute Stroke

Mahidol University1 site in 1 country19 target enrollmentStarted: August 6, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
19
Locations
1
Primary Endpoint
Five-Times-Sit-To-Stand test (FTSST)

Study Overview

Brief Summary

The aim of the present study is to evaluate the possible effect of using dual-tDCS applied during conventional physical therapy on lower limb function in stroke patients.

Detailed Description

Recently dual-tDCS applied before the conventional physical therapy show positive effect of lower limb performance. However to explore the time during which dual-tDCS can be combined with physical therapy to maximize motor performance is required. Results from the present study with be compared with our previous study that used dual-tDCS applied before physical therapy.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age range 18-75 years.
  • •First ever-ischemic lesion in the territory of middle cerebral artery or anterior cerebral artery. CT scan/MRI result is thus required.
  • •Sub acute phase of stroke (less than 6 months)
  • •Able to sit-to-stand and stand-to-sit independently
  • •Able to walk without physical assistance at least 6 m
  • •Free of any neurological antecedent, unstable medical conditions or condition that may increase the risk of stimulation such as epilepsy

Exclusion Criteria

  • •Pre-stroke disability
  • •Be unable to understand the instruction
  • •No clear neurological antecedent history or psychiatric disorder
  • •Excessive pain in any joint of the paretic limb (numerical pain rating score > 7)
  • •Presence of intracranial metal implantation, cochlea implant, or cardiac pacemaker
  • •Subjects are participating in the other protocol or receiving alternative treatment such as acupuncture

Arms & Interventions

Active tDCS & PT

Experimental

Dual transcranial direct current stimulation (tDCS) will be applied over the leg motor area (M1) during the first 20 mins of conventional physical therapy (about 1 hours). Anodal on affected hemisphere, Cathodal on unaffected hemisphere. Current intensity is fixed at 2 mA and current will flow continuously during 20. Physical therapist will give an intervention program exactly the same in all cases. The scope of intervention is administered to improve strength of weakened and postural lower limbs muscles such as trunk muscles, hip flexors/extensors/abductors, knee flexors/extensors.

Intervention: Transcranial direct current stimulation (Device)

Sham tDCS & PT

Active Comparator

Dual transcranial direct current stimulation (tDCS) will be applied over the leg motor area (M1) during the first 20 mins (sham mode) of conventional physical therapy (about 1 hours). Anodal on affected hemisphere, Cathodal on unaffected hemisphere. Physical therapist will give an intervention program exactly the same in all cases. The scope of intervention is administered to improve strength of weakened and postural lower limbs muscles such as trunk muscles, hip flexors/extensors/abductors, knee flexors/extensors.

Intervention: Transcranial direct current stimulation (Device)

Outcomes

Primary Outcomes

Five-Times-Sit-To-Stand test (FTSST)

Time Frame: 5 minutes

sling. Subjects will be instructed as the following "I want you to stand up and sit down 5 times as quickly as you can when I say 'Go'." Subjects must be fully standing between repetitions. Timing will begin at "GO" and ends when the patient's buttocks touch the seat after the fifth sit-to-stand.

Timed Up & Go test (TUG)

Time Frame: 5 minutes

Subjects will sits on the chair and place their back against the chair. Timing will begin at "GO", the subjects will be asked to walk 3m, turn, walk back, and sit down. The stopwatch stops when the patient's buttocks touch the seat.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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