Skip to content

The Effect of transcranial direct stimulationof different brain cortex areas plus the traditional physical therapy on pain and function of subjects with knee osteoarthritis

The Effect of transcranial direct stimulationof different brain cortex areas plus the traditional physical therapy on pain intensity and clinical functional ability of subjects with knee osteoarthritis: “A randomised controlled trial”

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181216042010N1
Enrollment
40
Registered
2018-12-25
Start date
2018-12-22
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

knee osteoarthritis. Unilateral primary osteoarthritis of knee

Interventions

Intervention 1: Intervention group: traditional Physiotherapy(Ultrasound, Infra-Red, Trans- cutaneous Electrical Nerve Stimulation, Exercise therapy) with trans-cranial direct current stimulation of

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 70 Years

Inclusion criteria

Inclusion criteria: Individuals aged 50-70 years Individuals with grades 2 and 3 of OA to the diagnosis of orthopedics by System Kellgren and Lawrence Having at least 3 signs of the 6 clinical symptoms of the American College of Rheumatology People with dominant right leg involvement (in the case of bilateral, the right lesion is also dominant) Minimal pain 4 according to the visual scale of pain

Exclusion criteria

Exclusion criteria: Having knee surgery for the last six months Replacing the knee joint or tibia osteotomy on the affected side Neurological conditions affecting organ function (Parkinson's disease, stroke and multiple sclerosis) Inability to walk without help History of another rheumatic disease that causes secondary osteoarthritis People with lack of sensation and epilepsy whom pain modification techniques are prohibited

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: before initiation of treatment, 10 session, 1 month ago. Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
Function. Timepoint: before initiation of treatment, 10 session, 1 month ago. Method of measurement: questionnaire and tests.;Strength of muscle. Timepoint: before initiation of treatment, 10 session, 1 month ago. Method of measurement: dynamometer.;Range of motion. Timepoint: before initiation of treatment, 10 session, 1 month ago. Method of measurement: goniameter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGholmhosein Nassaj

Ahvaz University of Medical Sciences

nassadj@yahoo.com+98 613337431011162

Outcome results

None listed

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