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Completed

NCT Number: NCT05811637

Investigation of the Effect of Pilates Exercises on Patellofemoral Pain

This study aimed to investigate the effectiveness of Pilates exercises in Patellofemoral pain patients compared to hip and knee combined exercises in improving pain, muscle strength, flexibility, function and quality of life in short term.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Istanbul University

Istanbul, Turkey (Türkiye)

About this study

Patellofemoral pain is a common condition characterized by pain in anterior knee, around the kneecap. It is known that exercise is beneficial in rehabilitation in general. Exercise programs applied to patients with PFP should include hip and knee-targeted combined exercises. Nowadays, Pilates is used as an effective rehabilitation tool for individuals with musculoskeletal problems, especially in reducing pain and improving function. Therefore, we believe that Pilates exercises can be effective in PFP Considering that PFP is a chronic condition and exercise therapy is one of the main strategies in the treatment. Pilates may be preferred as one of the alternative treatment method.

This randomized controlled study was designed to compare the effects of two different treatment protocols, Group-I (Supervised Rehabilitation) and Group-II (Pilates Exercises). Patients who applied to the Istanbul Physical Therapy and Rehabilitation Training and Research Hospital, Sports Medicine outpatient clinic and were diagnosed with PFP by a specialist physician based on the patient histories, physical examinations, and diagnostic imaging. The estimated desired sample size was at least 14 participants per group. We anticipated a dropout rate of 20%. Therefore, 34 participants were required for each group (Supervised Rehabilitation n=17, Pilates Exercises n=17) of both sexes, ages ranging from 18-45 years. A computer generated randomization list was used to divide the patients into two groups (https://www.randomizer.org/). An 'Informed Consent Form' was obtained from patients by explaining the purpose of the study, the duration of the study, the treatments to be applied, and possible side effects.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Having characteristic signs of PFP (retropatellar or peripatellar pain)
  • Presence of at least 3 points of retropatellar or peripatellar pain on the Numbered Pain Rating Scale (NPRS) with squatting, climbing stairs, prolonged sitting, or functional activity that burdens the PFP
  • Presence of any of the criteria such as tenderness, small effusion in the patellar facet palpation

Exclusion criteria

  • Patellofemoral dislocation, subluxation, intra-articular knee pathology
  • Previous lower extremity surgery, and knee-related trauma
  • A history of hip pathology or neurological disorders
  • Knee trauma in the last 1 month

Treatment and study plan

pilates exercise

Other

The program will be applied with the Pilates exercises every week. All patients were evaluated before and after the treatment (6 weeks).

Supervised rehabilitation

Other

The program will be applied with the progression of the supervised rehabilitation in the 4th week

Primary outcomes

  1. Functional assessment

    Time frame: 6 weeks

    Kujala Anterior Knee Pain Scale is used to assess the functional disability levels of the patients.

  2. Pain assessment

    Time frame: 6 weeks

    The numerical NPRS is used to measure and monitor the severity of pain. The patients will be asked to rate the severity of the current pain level between 0 and 10 (0 being "no pain" and 10 being the "worst imaginable pain").

Secondary outcomes

  1. Muscle strength assessment

    Time frame: 6 weeks

    Quadriceps strength will be measured using the Lafayette Manual Muscle Tester (Lafayette Instrument-model 01165, USA) handheld dynamometer.

  2. Muscle flexibility assessment

    Time frame: 6 weeks

    The flexibility of the hamstring muscles' length will be measured with the "Sit and Reach Test".

  3. Quality of life assessment

    Time frame: 6 weeks

    The short form SF-36v2 will be used to assess the quality of life. The scale, designed to assess the quality of life, covers physical, social, and psychological conditions.

Sponsors and collaborators

Lead sponsor

Istanbul University

Other

Registry information

Official study title

Istanbul University, Faculty of Health Science, Division of Physiotherapy and Rehabilitation

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Apr 13, 2023
Registry last updated
Nov 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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