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Effect of Short-term Motor Training on Accuracy and Precision of Knee Movement in Human With and Without Knee Pain

Not Applicable
Completed
Conditions
Knee Pain Chronic
Healthy Eld Human
Hypertonic Saline
Isotonic Saline
Interventions
Drug: Hypertonic saline
Drug: isotonic saline
Other: Motor training
Registration Number
NCT04146311
Lead Sponsor
Aalborg University
Brief Summary

The objects of this research are to investigate the ability of the motor learning and test the possible differences between younger and older healthy human, and between non-pain and acute experimental pain and chronic clinical pain conditions.

Detailed Description

The project consists of four experimental studies. In the first experiment, younger and older healthy human subjects are involved in a short-term neuromuscular training on the accuracy and precision of knee movement to investigate the possible age effect of the motor learning. The second experiment focuses on the experimental pain on the learning effect of the younger subjects. The third experiment will investigate a group of knee osteoarthritis patients to show the influence of chronic pain on the motor training compared with age-, gender-matched pain free subjects. 3D camera tracking system will be used to record the knee movements at the baseline and after 6-day motor task training. The variability in amplitude of the values of knee movements was transformed to percentage in relation to the target position (accuracy) or to the mean position (precision). The results of the study will contribute to both basic and clinical understanding of the mechanisms related to knee movement control and influences of varies painful conditions.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • • Aged 18-30 or 50-65 years

    • Free from ongoing or chronic pain
    • Right dominant leg
    • Speak and understand English
    • Aged 50-65 years.
    • Diagnosed with knee OA (according to American College of Rheumatology classification) with pain in left or both knees for more than six months
    • Have ongoing pain rated above 2 on a 0-10 Visual Analogues Scale (VAS) in the previous week.
    • Right dominant leg
    • Speak and understand English
    • Aged 50-65 years
    • Diagnosed with knee OA
    • Have had total knee arthroplasty on left or both knees
    • Right dominant leg
    • Speak and understand English
Exclusion Criteria
  • • Pregnancy or intent to become pregnant, breast feeding

    • Regular use of analgesics, including simple analgesia and NSAIDs
    • Frequent recreational drug or alcohol use
    • History of knee joint pathology or injury
    • Previous neurologic, musculoskeletal or mental illnesses
    • Practicing sport activities on a regular basis
    • Lack of ability to cooperate
    • Regular use of analgesics, including analgesia and NSAIDs for the last 24 hours
    • Frequent recreational drug or alcohol use
    • Previous neurologic, musculoskeletal or mental illnesses
    • Practicing sports activities on a regular basis
    • Lack of ability to cooperate
    • Regular use of analgesics, including analgesia and NSAIDs for the last 24 hours
    • Frequent recreational drug or alcohol use
    • Other disorders or injuries in the knee joints
    • Previous neurologic, musculoskeletal or mental illnesses
    • Practicing sports activities on a regular basis
    • Lack of ability to cooperate

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Hypertonic salineHypertonic salineA bolus injection (0.25 ml) of hypertonic saline (5%) is injected into the left infrapatellar fat pad.
Hypertonic salineMotor trainingA bolus injection (0.25 ml) of hypertonic saline (5%) is injected into the left infrapatellar fat pad.
Isotonic salineisotonic salineA bolus injection (0.25 ml) of isotonic saline (0.9 %) is injected into the left infrapatellar fat pad.
Isotonic salineMotor trainingA bolus injection (0.25 ml) of isotonic saline (0.9 %) is injected into the left infrapatellar fat pad.
Motor trainingMotor trainingAll the subjects recruited need to have a short-term motor task training at home. 30 times a session, totally 2 sessions a day for 6 days
Primary Outcome Measures
NameTimeMethod
knee movement assessmentChange from baseline, up to 7 days after the first session

There are two sessions in total, seperated by a 6 days motor training. Using 3D camera to calculate the accuracy and precision of knee movements at 30, 45, 60 degree respectively both with and without visual feedback (baseline), before and after motor training, also before and after injection.

Secondary Outcome Measures
NameTimeMethod
Assessment of painOnly on day 7 (second session), up to 24 hours

Immediately following the injection, participants will be instructed to rate the pain intensity for ten minutes using a digital visual analogue scale (VAS; eVas Software: Aalborg University, Denmark), on a tablet.The scale will be measured from 0 to10, where 0 represents 'no pain' and 10 represents 'worst pain imaginable'.

Trial Locations

Locations (1)

Aalborg University

🇩🇰

Aalborg, Denmark

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