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The effect of electroacupuncture and exercise therapy on pelvic surgery

Comparison of the effect of exercise therapy with electroacupuncture with exercise therapy with electrical percutaneous nerve motility on pain, physical function and gait in people with complete hip arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191208045652N4
Enrollment
20
Registered
2021-11-04
Start date
2021-12-21
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

Total Hip Arthroplasty (THA). Osteoarthritis of hip

Interventions

Intervention 1: Intervention group: the intervention group, the first session of treatment will use electroacupuncture along with exercise therapy.DZ-II NERVE AND MUSCLE STIMILATOR made in China in 2

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients undergoing hip arthroplasty surgery one to two days after surgery People aged 60 and over The surgical incision is anterior-external and the head of the hip bone and acetabulum have been replaced Patients' pain at the time of initial evaluation after surgery should be at least 3 cm based on a numerical pain rating scale Ability to read and write in cycles Ability to walk at least 50 meters History of neurological diseases that cause patients to be unable to function

Exclusion criteria

Exclusion criteria: Re-hip surgery Existence of infection after hip replacement surgery Partial loss of hip or acetabulum during study due to interventions History of using painkillers that are outside the treatment regimen of a specialist physician while studying or are different from other painkillers used by other patients Patients with diabetes, etc. who use painkillers to reduce joint pain

Design outcomes

Primary

MeasureTime frame
In this study, the amount of pain is the primary outcome variable because the sample size and inclusion criteria are determined based on this variable. Timepoint: Days 1, 5, 15 and 30 of the intervention. Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
Physical function. Timepoint: Days 1, 5, 15 and 30 of the intervention. Method of measurement: Hip Disability and Osteoarthritis Outcome Score (HOOS), Three tests of maximum walking speed, 3-minute walking test and sitting and standing up test.;Edema of the entire lower limb. Timepoint: Days 1, 5, 15 and 30 of the intervention. Method of measurement: Using a tape measure, the edema of the entire lower limb is measured in areas 10 cm above the knee joint, the middle part of the leg as well as the middle area of ??the foot.;Hip Range of motion. Timepoint: Days 1, 5, 15 and 30 of the intervention. Method of measurement: A goniometer is used to measure the range of motion of the hip joint.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzia Yassin

Iran University of Medical Sciences

m.yassin.pt@gmail.com+98 21 2222 8052

Outcome results

None listed

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