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Observation on the therapeutic effect of transcranial direct current combined with isokinetic strength training on lower limb function in stroke patients

Observation on the therapeutic effect of transcranial direct current combined with isokinetic strength training on lower limb function in stroke patients

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071380
Enrollment
Unknown
Registered
2023-05-12
Start date
2023-05-25
Completion date
Unknown
Last updated
2023-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Interventions

tDCS group:Transcranial direct current stimulation therapy
IST group: Isokinetic strength training therapy
combined group:Transcranial direct current+isokinetic muscle strength training

Sponsors

Xuzhou Rehabilitation Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Conforming to the stroke standards revised by the 4th National Conference on Cerebrovascular Disease in 1996, and confirmed by brain CT or MRI examination, the vital signs are stable ; 2.The first stroke, unilateral onset, with a course of less than 6 months ; 3.Age 20-80 years old ; 4.At least able to walk on their own or with the help of assistive devices, walk on flat indoor ground for at least 10 meters ; 5.No previous history of epilepsy ; 6.The subjects or their families signed the informed consent form ;

Exclusion criteria

Exclusion criteria: 1.Individuals with severe cognitive and communication barriers who are unable to cooperate; 2.Severe dysfunction of important organs such as the heart, lungs, and kidneys; 3.Wearing pacemakers or other implanted devices (such as electronic cochlea, built-in pumps, artificial heart metal valves, intraocular metal foreign bodies) or having skull defects; 4.Other conditions that can cause walking dysfunction, such as spinal cord injury, lower limb osteoarthritis, etc; 5.Unable to follow the research protocol for treatment or give up midway.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment-lower Extremities;Berg Balance Scale;Ten meter walking timing test;Ultrasound (muscle thickness and cross-sectional area of the rectus femoris and intermedius femoris);Balance instrument evaluation (motion ellipse area, motion length);Peak Torque;Peak Torque/Body Weigh;Knee flexor peak torque/knee extensor peak torque;

Secondary

MeasureTime frame
Modified Barthel index;Functional Ambulation Category scale;

Countries

China

Contacts

Public ContactZhang Ming

Xuzhou Rehabilitation Hospital

zm1455@163.com+86 189 5217 0642

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026