Skip to main content
OpenTrials
Completed

NCT Number: NCT04146311

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Aalborg University

Aalborg, 9220, Denmark

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Hypertonic saline

Drug

A bolus injection (0.25 ml) of hypertonic saline (5%) into the left infrapatellar fat pad.

Isotonic saline

Drug

A bolus injection (0.25 ml) of isotonic saline (5%) into the left infrapatellar fat pad.

Motor training

Other

All 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 outcomes

  1. knee movement assessment

    Time frame: Change 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 outcomes

  1. Assessment of pain

    Time frame: Only 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'.

Sponsors and collaborators

Lead sponsor

Aalborg University

Other

Registry information

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Oct 31, 2019
Registry last updated
Jan 13, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.