This interventional study, a randomized, single-blinded clinical trial, has been registered on Iran’s clinical trials website (ID No.:
IRCT20180416039323N4). The research was conducted in the clinical biomechanics research center and the physical medicine department of AJA University of Medical Sciences at Imam Reza Hospital in Tehran in 2023. The project was reviewed and approved by the Ethics Committee of AJA University of Medical Sciences based on the submitted documents (ID No.:
IR.AJAUMS.REC.1402.086) on July 17, 2023.
The inclusion criteria were soldiers diagnosed with CMP, aged 18 - 30 years, with a disease duration of more than 2 months, and lack of improvement with conservative treatments for at least one month. Chondromalacia patella was diagnosed based on the patient’s clinical symptoms, including anterior knee pain and, in some cases, posterior knee discomfort that is intensified by prolonged sitting with bent knees (theatre sign), going up and down stairs, and squatting. Exclusion criteria included a history of lower limb surgery or serious knee trauma within the last 6 months, mild trauma within the last 2 months, history of steroid drug use, coagulation problems, systemic diseases (e.g., diabetes, rheumatoid arthritis), scar at the acupuncture site, implantable cardiac defibrillators, programmable intrathecal devices, and/or disseminated cancer. Patients with evidence of intra-articular or extra-articular injury diagnosed by examination or radiography were also excluded.
Patients meeting the inclusion criteria were examined by the study researchers. Knee X-rays in frontal and lateral views were obtained to rule out any structural abnormalities. All study steps were explained to the patients, and signed written consent was obtained. One leg of each patient was included in the study, and if both legs had symptoms, the knee with more severe symptoms was included.
In the electroacupuncture group, patients lay quietly on the bed while treatment was administered at acupuncture points ST34, ST36, ST38, SP9, SP10, and GB34 using 0.3 × 30 mm sterile needles with a penetration depth of 10 mm for 20 minutes. An electroacupuncture device (Hwato Electronic Acupuncture Stimulator Sdz-II, made in China) was used to generate current with a frequency of 5 - 20 Hz and an intensity within the patient’s tolerance range, ensuring no significant muscle twitch. In the physical therapy group, patients underwent 10 sessions of routine physical therapy modalities, including infrared, ultrasound, and transcutaneous electrical nerve stimulation (TENS), for a total of 20 minutes. Both groups received 10 consecutive daily sessions. Patients were advised not to take any particular drug, but in cases of severe pain, they could take acetaminophen 325 mg once a day. Stretching exercises for the calf and hamstring muscles and strengthening exercises for the quadriceps muscles were taught to the patients in both groups.
The VAS score was used to evaluate primary outcomes such as pain and disability, with a 10 cm VAS measuring pain and disability subjectively from 0 (no pain) to 10 (most severe pain). Secondary outcomes were evaluated using the KOOS questionnaire, a self-report questionnaire covering pain, symptoms, daily activities, recreation, and quality of life. Each item is scored from zero to four, with subscales calculated on a score from zero (severe symptoms) to 100 (no symptoms). The Persian version of the KOOS questionnaire was validated in a study on 147 patients with knee problems (
11).
Patients were assigned to one of the two groups using the block randomization method, ensuring equal group sizes of 22 participants each (44 patients overall). Block randomization with varying block sizes was used, and permutations for equal group sizes were randomly selected. Random numbers were generated using random allocation software version 1. The individuals explaining and recording the outcome questionnaires and the analyst were blinded to patient allocation.
Data analysis was performed using SPSS software version 26. Results were reported as mean and standard deviation (mean ± SD). The Kolmogorov-Smirnov test assessed the normal distribution of each group of data. The independent t-test compared the means between the two groups, while repeated measures ANOVA compared mean repetitions over time. Mixed ANOVA was also used to compare these repetitions between groups.