--- title: Rigid Taping and Patella Stabilizing Brace Methods in pwPFPS (Patient With Patellofemoral Pain Syndrome) nct_id: NCT05629286 overall_status: COMPLETED sponsor: Istanbul University - Cerrahpasa study_type: OBSERVATIONAL primary_condition: Patellofemoral Pain Syndrome countries: Turkey (Türkiye) canonical_url: "https://parkinsonspathways.com/agent/trials/NCT05629286.md" clinicaltrials_gov: "https://clinicaltrials.gov/study/NCT05629286" ct_last_update_post_date: 2024-12-27 last_seen_at: "2026-05-12T07:04:32.885Z" source: ClinicalTrials.gov (mirrored, no enrichment) --- # Rigid Taping and Patella Stabilizing Brace Methods in pwPFPS (Patient With Patellofemoral Pain Syndrome) **Official Title:** Immediate Effect of Rigid Taping and Patella Stabilizing Brace on Proprioception, Functionality, and Balance in Patients With Patellofemoral Pain Syndrome **NCT ID:** [NCT05629286](https://clinicaltrials.gov/study/NCT05629286) ## Key Facts - **Status:** COMPLETED - **Study Type:** OBSERVATIONAL - **Target Enrollment:** 36 - **Lead Sponsor:** Istanbul University - Cerrahpasa - **Conditions:** Patellofemoral Pain Syndrome - **Start Date:** 2023-02-01 - **Completion Date:** 2024-12-22 - **CT.gov Last Update:** 2024-12-27 ## Brief Summary Patellofemoral pain syndrome (PFPS) is a common musculoskeletal disease with an annual prevalence of 22.7%. Pain in the anterior of the knee and/or retropatellar and/or peripatellar region patellofemoral compression force increases, squatting, climbing stairs, prolonged sitting is characterized by increased pain related activities such as flexion after. A large number of different treatment strategies have been proposed to examine these underlying factors and to address the resulting disorders and activity limitations. PFPS in the conservative treatment of patellar taping, stretching the shortened structures, the vastus medialis obliquus, strengthening activity modification, biofeedback, neuromuscular electrical stimulation, ultrasound, and foot orthoses and brace is located. The most frequently used for the treatment of patients with high effect size physiotherapy treatment and exercise training combined treatment in order to control the pain in the short and medium term, while the external knee supports-foot orthoses (brace), kinesiotape, rigid-band is used. It is known that the most commonly recommended external support for patients in the fight against PFPS in the clinical setting is kinesiological taping and brace. However, since kinesiotaping does not show orthotic properties like brace, their comparison with each other and the study of their effects give misleading results. The use of McConnell taping, which can show similar effects with both kinesiotaping and brace, gives clinically positive results. When the literature was examined, there was no study that examined the effectiveness of brace and rigid taping comparatively. In our study, we aim to investigate the extent to which we can change the impaired patella position in PFPS with the use of rigid tape and brace in accordance with this information in the literature and to examine the possible effects of rigid tape and brace, which we will apply to patients with PFPS, on balance, proprioception, gait and functionality in patients. In line with the results we will obtain, it is aimed to increase the effectiveness of treatment and shorten the recovery time by determining the external support that will help patients exercise and their movements in daily life. H1: McConnell taping and patella stabilizing brace applications applied to patients with PFPS differ from each other in terms of proprioception, functionality, balance and gait parameters. ## Detailed Description Voluntary participants who have been diagnosed with PFPS and agreed to voluntary health subjects will be included in the study. Signed voluntary consent will be obtained from participants. Participants will be divided into tree groups. One of the intervention groups will be taped first, then brace; the other will be used brace first, then tape. Healthy individuals will form the control group. ## Eligibility - **Minimum age:** 18 Years - **Maximum age:** 50 Years - **Sex:** ALL - **Healthy Volunteers:** Yes ``` Inclusion Criteria: * being 18-50 years old * Having been diagnosed with patellofemoral pain syndrome * BMI \<30 kg/m2 * For the last 3 months, the pain in the front of the knee in descending stairs, squatting and functional activities has been \> 3 points on the visual analog scale Exclusion Criteria: * The presence of an organic lesion (chondromalesia patella, syndrome of excessive lateral pressure, peripatellar bursitis, bening-malignant neoplasm, tendonitis) that can cause pain in the front of the knee * Having had steroid injections in the knee within the last 6 months and/or having received a physiotherapy program for the knee * Having undergone lower extremity surgery * Having a diagnosis of Grade 2 and above osteoarthritis according to Kellgren Lawrence * Presence of Patellar Tendinopathy * Presence of a history of trauma to the lower extremities * The presence of neurological problems that will affect balance and walking * Having any rheumatological disease * The use of an assistive device for the ambulance ``` ## Arms - **Intervention Group 1** — McConnell taping first and then patella stabilizing brace applied to healty participants and patients with PFPS - **Intervention Group 2** — first patella stabilizing brace and then applied McConnell taping to healty participants and patients with PFPS - **No Intervention Group** — no intervention to healty participants and patients with PFPS ## Interventions - **McConnell taping** (DEVICE) — non-stretch rigid McConnell tape will be applied - **Patella Stabilizer Brace** (DEVICE) — An orthotic application that wraps the patellofemoral joint, which has a patellar cavity and supports the patella, and provides stabilization with velcro ## Primary Outcomes - **Kujala Patellofemoral Scoring** _(time frame: up to three weeks)_ — It is a tool that allows functional evaluation in knee complaints due to patellofemoral structure. - **Visual Analog Scale** _(time frame: up to three weeks)_ — The maximum pain intensity assessment of the participants during walking, climbing stairs, descending stairs, sitting and squatting activities will be performed using a 10 cm VAS. ## Secondary Outcomes - **10 Stair Up Test** _(time frame: up to three weeks)_ - **Squat** _(time frame: up to three weeks)_ - **Joint Position Sense** _(time frame: up to three weeks)_ - **Single Leg Stance Test** _(time frame: up to three weeks)_ - **Y Balance Test** _(time frame: up to three weeks)_ ## Locations (1) - Istanbul University-Cerrahpaşa, Istanbul, Turkey (Türkiye) ## Recent Field Changes (last 30 days) - `eligibility.sex` — added _(2026-05-12)_ - `status.overallStatus` — added _(2026-05-12)_ - `status.primaryCompletionDate` — added _(2026-05-12)_ - `status.completionDate` — added _(2026-05-12)_ - `status.lastUpdatePostDate` — added _(2026-05-12)_ - `design.enrollmentCount` — added _(2026-05-12)_ - `eligibility.criteria` — added _(2026-05-12)_ - `eligibility.minAge` — added _(2026-05-12)_ - `eligibility.maxAge` — added _(2026-05-12)_ - `outcomes.primary` — added _(2026-05-12)_ - `outcomes.secondary` — added _(2026-05-12)_ - `armsInterventions.arms` — added _(2026-05-12)_ - `armsInterventions.interventions` — added _(2026-05-12)_ - `sponsor.lead` — added _(2026-05-12)_ - `results.hasResults` — added _(2026-05-12)_ - `locations.istanbul university-cerrahpaşa|istanbul||turkey (türkiye)` — added _(2026-05-12)_ --- *Canonical: https://parkinsonspathways.com/agent/trials/NCT05629286.md* *Source data (authoritative): https://clinicaltrials.gov/study/NCT05629286* *This page is a raw mirror with no AI summary, no editorial enrichment, and no Parkinson's-specific filtering.*