Knee Extensor Muscle Properties in Young Women Symptomatic and Asymptomatic for Anterior Knee Pain

Sponsor
Federal University of Rio Grande do Sul (Other)
Overall Status
Completed
CT.gov ID
NCT02734030
Collaborator
(none)
32
1
18
1.8

Study Details

Study Description

Brief Summary

This study aims to compare the knee extensors' mechanical, morphological and myoelectric properties between subjects affected by anterior knee pain and a healthy control group. The investigators hypothesis is that patients with anterior knee pain present a reduction in the knee extensors' mechanical, morphological and myoelectric properties due to chronic muscle inhibition produced by the syndrome. In addition, the study also aims to evaluate whether there are differences in methodology for application of the Interpolated Twitch Technique for evaluation of the quadriceps muscle inhibition by comparing the use of supramaximal electrical stimulation on the femoral nerve (gold standard) with stimulation on the motor point (new methodology) in healthy subjects and individuals affected by anterior knee pain. The investigators hypothesis is that the stimulation on the motor point is less discomfortable than on the femoral nerve and muscle inhibition results are less variable (with lower dispersion) due to such lower discomfort

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Participants were divided in two groups (control group, n=16 and anterior knee pain group, n=16). Prior to participation, informed consent was obtained from all subjects. The evaluation was performed at the lower limb with severe symptoms of anterior knee pain in the patients, and at the dominant limb in the control group. Quadriceps Muscle inhibition was estimated using the Interpolated Twitch Technique, which involves applying a single electrical twitch stimulation to the femoral nerve (gold standard) during a maximal isometric knee extensor contraction. Muscle inhibition measurements were obtained with the aid of a Grass S88 (Quincy, MA, USA.) Muscle Stimulator in combination with and isolation unit approved for human use. Isometric and isokinetic knee extensor torques were obtained with a Biodex System 3 dynamometer (Biodex Medical System, Shirley - NY, USA). Electromyographic muscle activity was measured with bipolar surface electrodes (Kendall, Meditrace - 100; Ag/AgCl) that were placed on the muscle bellies of vastus medialis, vastus lateralis and rectus femoris. Muscle architecture was measured with a B-mode ultrasonographic system (SSD; Aloka Inc., Tokyo, Japan) with a linear-array probe (60 mm, 7.5MHz; Aloka). Single Leg Squat was used for clinical evaluation of the lower limb functionality.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    32 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Knee Extensor Muscle Inhibition and Neuromechanical and Morphological Properties in Young Women Symptomatic and Asymptomatic for Anterior Knee Pain
    Study Start Date :
    Apr 1, 2015
    Actual Primary Completion Date :
    Mar 1, 2016
    Actual Study Completion Date :
    Oct 1, 2016

    Arms and Interventions

    Arm Intervention/Treatment
    Control Group

    Knee pain-free females with no history of lower limb injuries serving as a control group. .

    Anterior Knee Pain Group

    Females with anterior knee pain syndrome were enrolled in this group.

    Outcome Measures

    Primary Outcome Measures

    1. Torque [Torque was measured during a single visit to the laboratory during the study.The evaluation was performed up to 5 months]

      Torque is an expression of the muscular strength and was assessed by dynamometry.

    2. Muscular architecture [Muscle architecture was measured one time during the study. The evaluation was performed up to 5 months]

      Muscular architecture (muscle thickness, pennation angle and fascicle length) was assessed by ultrasonography

    3. Muscle inhibition [Muscle inhibition was measured during a single visit to the laboratory during the study. The evaluation was performed up to 5 months]

      Quadriceps muscle inhibition was assessed using the Interpolated Twitch Technique comparing the use of supramaximal electrical stimulation on the femoral nerve (gold standard) with stimulation on the motor point (new methodology).

    4. Muscular electrical activation [Muscular electrical activation was measured during a single visit to the laboratory during the study. The evaluation was performed up to 5 months]

      Electrical activation was assessed by surface electromyography (EMG)

    5. Patellofemoral cartilage thickness [Patellofemoral cartilage thickness was measured one time during the study. The evaluation was performed up to 5 months]

      Patellofemoral cartilage thickness were assessed by ultrasonography

    6. Single Leg Squat [Single leg squat performance was measured one time during the study. The evaluation was performed up to 5 months]

      Single leg squat was measured with a video camera and allowed to determine lower limb functionality

    Secondary Outcome Measures

    1. Knee pain [Knee pain during the tests was measured after all knee extensor contractions. The evaluation was performed up to 5 months.]

      Knee pain was measured with a Visual Analogue Scale

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 40 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Anterior Knee pain group:
    1. Retropatellar or peripatellar knee pain in at least 2 of the following functional activities: stair ascent or descent, running, kneeling, squatting, prolonged sitting, jumping;

    2. Score smaller than 85 points on the Kujala Questionnaire;

    3. Physically active according to the International Physical Activity Questionnaire (IPAQ - short version)

    4. Body mass index less than 30

    • Control group:
    1. Knee pain-free females with no history of lower limb injuries
    Exclusion Criteria:
    1. Body mass index higher than 30

    2. Sedentary subjects

    3. Cardiovascular, neurological or cognitive disorders

    4. Any cardiorespiratory, neuromuscular, or metabolic disease that could represent an absolute contraindication or a contraindication to the performance of maximum strength tests

    5. Previous surgery on lower limb

    6. Participation in a strength-training programme or physiotherapy treatment for knee injuries in the past six months

    7. Otherwise associated injury in the lower limb joints other than anterior knee pain syndrome

    8. Pregnancy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Exercise Research Laboratory, School of Physical Education, Federal University of Rio Grande do Sul Porto Alegre Rio Grande do Sul Brazil 90690-200

    Sponsors and Collaborators

    • Federal University of Rio Grande do Sul

    Investigators

    • Principal Investigator: Marco Vaz, PhD, Federal University of Rio Grande do Sul

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Marco Aurélio Vaz, PhD, PhD, Federal University of Rio Grande do Sul
    ClinicalTrials.gov Identifier:
    NCT02734030
    Other Study ID Numbers:
    • UFRGS - 1.032.452
    First Posted:
    Apr 12, 2016
    Last Update Posted:
    Oct 26, 2017
    Last Verified:
    Oct 1, 2017
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by Marco Aurélio Vaz, PhD, PhD, Federal University of Rio Grande do Sul
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 26, 2017