patellofemoral pain syndrome
Conditions
Interventions
experimental group:Halo sport + dry needle therapy
control group:Dry needle therapy
Sponsors
Department of sports medicine, Shenzhen Hospital, Peking University
Eligibility
Sex/Gender
All
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: 1. Aged 18-40 years; 2. Non-traumatic knee pain, lasting 3-12 months; 3. More than 2 of the following movements are accompanied by knee pain (jumping, kneeling, sedentary, quadriceps contraction, running, squatting, stair climbing, or putting pressure on the patella); 4. Anterior knee pain score <85 points (Anterior Knee Pain Scale, out of 100); 5. Able to obtain informed consent.
Exclusion criteria
Exclusion criteria: 1. History of knee joint infection, history of knee joint surgery, knee joint ligament instability, meniscus injury; 2. During pregnancy or lactation; 3. Currently participating in other clinical trials; 4. People with mental illness or cognitive impairment; 5. Subjects who have received any treatment with PFPS within the past 3 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| pain visual analogue scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| AKPS score; | — |
Countries
China
Contacts
Public ContactYou Tian
Department of sports medicine, Shenzhen Hospital, Peking University
Outcome results
None listed