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Benefits of functional training in women with knee pain.

Not Applicable
Conditions
Patellofemoral Pain Syndrome
Patellofemoral disorders
Women.
C05.550.700
M22.2
M01.975
Registration Number
RBR-8c7267
Lead Sponsor
niversidade Federal de Uberlândia
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Data analysis completed
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

Subjects must sign the Free and Informed Consent Form before starting the study activities; Aged between 18 and 30 years;
Active womens, who perform any physical activity up to twice a week; Presence of anterior or retropatellar pain in the knee for at least the last 3 months in two or more of the following activities: running, walking, jumping, climbing and/or descending stairs while remaining seated or kneeling for an extended period of time, Squatting position during the isometric extension of the knee with 60º of flexion, and/or during palpation of the medial or lateral facet of the patella; Presence of dynamic valgus during the unipodal squatting.

Exclusion Criteria

Will be excluded, individuals submitted to recent physiotherapeutic treatment; With history of knee surgery; Patellar instability; Ankle or hip injuries; Meniscal or ligament injury; Joint swelling of the knee, or any other specific knee change; Tendinitis in the lower extremity; Low back pain; Pain in the sacroiliac joints; pregnancy; Presence of any neurological disorders / disorders that compromise the understanding of the procedure, or that affect motor control; Any cardiovascular changes and rheumatic diseases.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary outcomes will be evaluated in two moments: pre and post treatment.<br>- Pain, evaluated by Visual Analogic Scale;<br>- Kinematics of the trunk and lower limb, evaluated during Single Leg Squat;<br>- Function, evaluated by Questionnaires: Anterior Knee Pain Scale and Activities Daily of Living Scale.<br><br>Is expected the reduction of at least 2 pain points at rest and in the activities of daily living after the intervention, when compared to the pre-intervention state, in both groups. However, it is believed that group 2 will have less pain when compared to group 1, after treatment.<br><br>It is expected that when comparing the pre and post-intervention moments, the is flexion anterior of the trunk and the dynamic valgus is lowest in both groups, being the largest reduction in group 2.<br><br>It is believed that after an intervention, a functionality of both groups is greater, being more evidenced in group 2.
Secondary Outcome Measures
NameTimeMethod
The secondary outcome will be evaluated in two moments: pre and post treatment.<br>- Force quadriceps muscles, knee extensor, gluteus medius and lateral rotators. Evaluated by Isometric dynamometer Lafayette Instrument Company)<br><br>It is expected that after treatment, the force will be significantly higher compared to the pre-intervention state, and that group 2 presented better strength when compared to group 1.
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