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Effectiveness of superimposed neuromuscular electrical stimulation in combination with strength training for patellofemoral pain syndrome: a randomized controlled pilot triall

Effectiveness of superimposed neuromuscular electrical stimulation in combination with strength training for patellofemoral pain syndrome: a randomized controlled pilot triall

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075636
Enrollment
Unknown
Registered
2023-09-11
Start date
2023-09-11
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Patellofemoral Pain Syndrome

Interventions

Superimposed Group:Neuromuscular electrical stimulation combined with strength training
Control Group:strength training

Sponsors

Beijing Sport University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) Age range from 18 to 40 years old; (2) Unilateral or bilateral anterior knee joint pain for 4 weeks (when bilateral pain occurs, the side with stronger pain intensity will be considered as the affected side according to VAS score evaluation); (3) Pain around or behind the patella, aggravated by at least one activity during prolonged sitting, climbing stairs, squatting, running, kneeling, or jumping. (4) Symptoms not caused by trauma; (5) At least two of the following tests are positive: palpation of pain at the posterior edge of the patella; Pain during squatting; Positive patellar grinding test; The quadriceps muscle contraction test was positive. (6) The patient accepts and cooperates with the treatment, and agrees to sign an informed consent form; Not receiving any medication or physical therapy.

Exclusion criteria

Exclusion criteria: (1) A history of patellar dislocation or subluxation, cartilage injury, or ligament relaxation; (2) Suspected patellar tendon disease, local patellar tendon pain; (3) Previous knee surgery or arthritis; (5) other knee joint injuries such as meniscus or ligament; (6) Patients contraindicated by low-frequency electrotherapy and those who could not tolerate electrical stimulation; (7) Presence of neurological, cardiovascular or blood-related diseases; (8) The knee joint is locked and/or soft; (9) Concurrent acute or chronic diseases; (10) Surgical history or surgical plans for other lower limb problems; (11) The patient is participating in other lower limb training programs; (12) Poor health, pregnancy or breastfeeding, etc.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale;Anterior knee pain scale;

Secondary

MeasureTime frame
Quadriceps muscle strength;Quadriceps muscle thickness;

Countries

China

Contacts

Public ContactYang Zhang

Beijing Sport University

bigbillzhang@163.com+86 188 1083 5913

Outcome results

None listed

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