A Controlled Trial on Recreational Runners With Patellofemoral Pain

Laval University

Status: Completed

Conditions: Patellofemoral Pain (PFPS)

Treatments: Other: Exercise program; Other: Education; Other: Gait retraining

Study type: Interventional

Funder types: Other

Identifiers

NCT02352909

PFC-2014 (Other Grant/Funding Number)

2014-15-1 (OPPQ-REPAR)

Details and patient eligibility

About

From a rehabilitation point of view, while several approaches exist to retrain runners with PFPS, it is not clear which one is most effective, or why. The goals of this randomised-controlled trial are: 1) to compare the effectiveness of three rehabilitation programs on pain and functional limitations of runners with PFPS and 2) to explain why the programs are effective or not based on laboratory analyses. After baseline evaluation, runners will be randomly assigned to one of three treatment groups, each with a specific 8-week rehabilitation program aimed at addressing the efficiency of a specific type of retraining. These groups are: 1) Control; 2) muscle recruitment; 3) reducing knee loading during running.

The investigators hypothesis is that the intervention targeting a reduction in knee loading will be significantly more effective in reducing symptoms and improving function of runners with patellofemoral pain syndrome.

Full description

Hypothesis will be tested using symptoms and functional status questionnaires. In addition, mechanistic analyses will be conducted using a running assessment using an instrumented treadmill and kinematics analyses.

Enrollment: 69 patients

Sex: All

Ages: 18 to 45 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Running mileage at least 15km
• Symptoms since at least 3 months
• Pain level at least 3/10 during running and 3 activities among: kneeling, squatting, stairs and resisted knee extension
• Score lower than 85/100 on the KOS-ADLS

Exclusion criteria

• History of knee surgery or patellar dislocation
• Pain believed to originate either from meniscus or from patellar tendon
• Pain following an acute trauma
• Concurrent lower limb injuries
• History of neurological, inflammatory, rheumatoid disease

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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69 participants in 3 patient groups

Control

Active Comparator group

Description:

Education will be given on how to modify running training to encourage improvement of symptoms.

Treatment:

Other: Education

Muscle recruitment

Experimental group

Description:

Subjects will receive an additional exercise program targeting non task-specific strengthening and motor control exercises of the lower limb.

Treatment:

Other: Exercise program

Other: Education

Reduction of knee loading

Experimental group

Description:

Subjects will receive additional personalized advice on how to modify running gait in order to reduce mechanical loads at the knee (gait retraining).

Treatment:

Other: Gait retraining

Other: Education