Skip to content

effect of neurodynamic mobilization and dry needling technique in subjects with patellofemoral pain syndrome

Comparison of the effect of neurodynamic mobilization and dry needling technique on the pain, function, and range of motion in subjects with patellofemoral pain syndrome

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240211060958N2
Enrollment
120
Registered
2024-06-02
Start date
2024-06-21
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

patellofemoral pain syndrome. Pain in knee

Interventions

Intervention 1: Intervention group: Dry needling. The treatment is done in 3 sessions with an interval of one day. The muscles selected

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: All participants are aged from 18 to 40 years Having a clinical diagnosis of patellofemoral syndrome. Complaints of pain in the anterior of the knee or around the patella on the affected side are determined during at least 3 of the following activities: squatting, step up and down from stairs, running, prolonged sitting, and kneeling. Positive Clark test Unilateral pain in one knee having constant pain for at least the last 4 weeks and the average pain in the last week is more than 3 according to the NPRS scale. The present of trigger points in the gluteus medius and quadriceps muscles on the same side and quadratus lumborum on the opposite side.

Exclusion criteria

Exclusion criteria: History of previous knee surgery Any knee pathology (meniscus tear, patella tendinopathy, ligament sprain and osteoarthritis) Any systemic diseases and/or connective tissue disorders People who have received acupuncture, injections, or dry needling treatment for knee in the past 6 months. Pregnant women

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Before, After and 1month follow up. Method of measurement: Visual analog scale.

Secondary

MeasureTime frame
Knee disability index. Timepoint: Before, After and 1month follow up. Method of measurement: kujala questionnaire.;Step down test. Timepoint: Before, after and 1month follow up. Method of measurement: Functional test: Participants are asked to stand on the step with their injured foot, try to touch the ground with the opposite heel, and then return to their original position.;Knee range of motion. Timepoint: Before, after and 1month follow up. Method of measurement: Goniometer.

Countries

Iran (Islamic Republic of)

Contacts

Public Contacttahereh rezaeian

Kerman University of Medical Sciences

tahere.rezaiyan@gmail.com+98 34 3132 5700

Outcome results

None listed

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