The Effect of a Treatment Protocol Focused on Neuromuscular Control Exercises on Pain and Function in a Subgroup of Individuals With Patellofemoral Pain

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-40
SponsorUniversidade do Porto

About this trial

Patellofemoral Pain (PFP) is one of the most common causes of knee pain and is significantly present in recreational athletes who have previously been categorized as being in a subgroup of PFP. Understanding which intervention is most appropriate for this subgroup could give us important information about subgroup-based treatments, which are not yet described in the literature. Therefore, the aim of this study is to analyze the effect of two exercise interventions in a PFP subgroup: one focusing on neuromuscular control exercises and the other focusing on muscle strengthening.This study will recruit 10 individuals to each exercise group, and will assess pain, function, muscle activity and joint kinematics pre and post intervention. Mixed Model ANOVA tests will be used to determine the responses to the two interventions between the two groups over a 6-week treatment time.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Pain during resisted isometric quadriceps contraction

Pain with palpation of the posterior borders of the patella

Pain during squatting Classified as being within the strong subgroup of PFP (exemplified in the following sections).

Disqualifiers

Individuals who are not part of the 'strong' PFP group

Previous knee surgery and participants awaiting surgery for another lower limb joint problems

Ligamentous instability and/or internal pathology

History of patella subluxation or dislocation

Trial design

Design model

Parallel

Treatments tested in this trial

  • Exercise

    Other intervention

    Balance and proprioceptive exercises

  • Muscle strengthening

    Other intervention

    Strengthening of the lower limb muscles

Treatment groups

24 Participants
are divided into 2 treatment groups
Group A: Neuromuscular control exercisesExperimental treatment 1 intervention
Group B: Muscle strengtheningActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Pain intensity

Full name: Numerical Pain Rating Scale (NPRS) Minimum value: 0; Maximum value: 10. Direction: Higher scores indicate a worse outcome, that is, greater pain intensity. Interpretation: 0: no pain 1-3: mild pain 4-6: moderate pain 7-10: intense/severe pain

Time frame
From enrollment to the end of treatment at 6 weeks

Secondary outcomes

1

Specific Knee Function

Full name: Anterior Knee Pain Scale (AKPS) Minimum value: 0 Maximum value: 100 Direction: higher scores indicate a better outcome (fewer symptoms and better knee function). General interpretation: 100 represents an absence of limitations/symptoms, while 0 represents greater functional impairment.

Time frame
From enrollment to the end of treatment at 6 weeks
2

General function

Full name: Knee injury and Osteoarthritis Outcome Score - Physical Function Shortform (KOOS-PS) Minimum value: 0 Maximum value: 100 Direction: higher scores indicate a worse outcome (greater difficulty/limitation in physical function). Interpretation: 0 = no functional difficulty; 100 = extreme functional difficulty.

Time frame
From enrollment to the end of treatment at 6 weeks
3

Kinesiophobia

Full name: Tampa Scale for Kinesiophobia (TSK-13) Number of items: 13 Minimum score: 13 Maximum score: 52 Direction: higher scores indicate a worse outcome, corresponding to a greater fear of movement/re-injury (kinesiophobia).

Time frame
From enrollment to the end of treatment at 6 weeks
4

Pain Catastrophizing

Full name: Pain Catastrophizing Scale (PCS) Number of items: 13 Minimum score: 0 Maximum score: 52 Direction: higher scores indicate a worse outcome, corresponding to a higher level of pain catastrophizing.

Time frame
From enrollment to the end of treatment at 6 weeks

Other outcomes

Sponsors and contacts

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