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Therapeutic effect of Electro-Acupressure stimulation in knee osteoarthritis

Evaluation of therapeutic effect of Electro-Acupressure stimulation in acupuncture points in reducing pain and stiffness and increasing knee joint function in patient with knee osteoarthritis: A randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211123053162N1
Enrollment
126
Registered
2022-08-31
Start date
2022-09-03
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Knee osteoarthritis. Osteoarthritis of knee

Interventions

Intervention 1: intervention group (1): Simultaneous electrical and pressure stimulation. Patients receive both electrical pulse and pressure simultaneously at eight acupuncture points around the knee

Sponsors

Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients over 45 years old Patients who have been suffering from osteoarthritis of the knee for at least three months (according to the diagnosis of a rheumatologist).

Exclusion criteria

Exclusion criteria: Patients who have had a history of acupuncture points stimulation for any purpose in the past month. Patients who have wound, scratch or abnormality in acupuncture points. Patients who have used anticoagulants in the past month and also patients who have had a history of coagulation diseases in the past month. Patients with a history of knee joint surgery (knee replacement). Patients who have advanced neuropathy (pain, burning, tingling in the toes or feet and extreme sensitivity to surface touch). Patients who are drug abuser. Patients who have had any injection into the knee joint in the past month. Patients who had a knee arthroscopy (a type of knee surgery that diagnoses and treats a knee joint problem) for 30 days prior to the intervention. Patients who have unbearable severe pain in the knee that prevents them from participating in the study. Patients with pacemakers. Patients with transplanted tissue. Pregnant patients.

Design outcomes

Primary

MeasureTime frame
Knee Pain. Timepoint: Before the first session, two days after the last session and three weeks after the last session. Method of measurement: WOMAC and KOOS questionnaire, VAS ruler.

Secondary

MeasureTime frame
Knee joint stiffness. Timepoint: Before the first session, two days after the last session and three weeks after the last session. Method of measurement: WOMAC and KOOS questionnaire.;Clinical manifestation of the knee joint. Timepoint: Before the first session, two days after the last session and three weeks after the last session. Method of measurement: WOMAC and KOOS questionnaire.;Ability to perform daily tasks. Timepoint: Before the first session, two days after the last session and three weeks after the last session. Method of measurement: WOMAC and KOOS questionnaire.;Physical activity. Timepoint: Before the first session, two days after the last session and three weeks after the last session. Method of measurement: KOOS questionnaire.;Quality of life. Timepoint: Before the first session, two days after the last session and three weeks after the last session. Method of measurement: KOOS questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Javad Hashemi

Shahroud University of Medical Sciences

mohammadjavad.hashemi027@gmail.com+98 23 3239 5054

Outcome results

None listed

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