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Efficacy of different physiotherapy methods in the rehabilitation of patients with knee osteoarthritis

Efficacy of Action Potential Simulation and Interferential therapy in the rehabilitation of patients with knee osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201403024641N8
Enrollment
70
Registered
2014-03-06
Start date
2012-08-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Knee Osteoarthritis. Polyarthrosis, unspecified

Interventions

Intervention 1: First group will undergo Action potential stimulation (APS) 10-15 minutes each session for 10 session.ll patients (both groups) in physiotherapy sessions will receive the usual physica
Rehabilitation
First group will undergo Action potential stimulation (APS) 10-15 minutes each session for 10 session.ll patients (both groups) in physiotherapy sessions will receive the usual physical modalities equ
Second group will undergo inferential therapy (IFT) 10-15 minutes each session for 10 sessions.ll patients (both groups) in physiotherapy sessions will receive the usual physical modalities equally.

Sponsors

Physical medicine and rehabilitation researches center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Mild or moderate knee osteoarthritis based on American College of Rheumatology criteria. Exclusion criteria: Age under 50 years old; Rheumatologic disease; History of knee surgery; Lower limbs fracture with knee joint involvement; Severe knee osteoarthritis; Electrical implants like pacemaker; Heart conduction block disease; Epilepsy; Cancers; Pregnancy; Lower limbs thrombosis; Couldn't complete questioners for any reason; knee joint injection in previous 6 month; Balance control deficit; Neuropathy or sensory deficit; Skin breakdown in knee region.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain relief. Timepoint: Before intervention and two months later. Method of measurement: Visaul Analogue Scale.

Secondary

MeasureTime frame
Function Improvement. Timepoint: Before intervention and two months later. Method of measurement: Western Ontario and McMaster Universities Arthritis Index (WOMAC).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Bina Eftekharsadat

Tabriz University of Medical Sciences

binasadat@yahoo.com+98 41 1336 1928

Outcome results

None listed

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