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An investigation of how rigid strapping tape fatigue impacts ankle and knee function during a cutting task

An investigation of how rigid strapping tape fatigue impacts ankle and knee function during a cutting task

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12617000773336
Enrollment
42
Registered
2017-05-26
Start date
2017-07-24
Completion date
2017-09-20
Last updated
2018-06-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Lower limb pathology is the most common form of disability among sporting populations, accounting for over 50% of all sporting injuries. Taping is routinely recommended with the expectation it restricts joint range of motion, and therefore reduces the risk of injury. While the effects of taping have been well investigated in the literature, gaps still exist around the effect of ankle strapping on knee function, and whether ankle movement increases as strapping tape fatigues. Gaining a better understanding of the relationship ankle strapping has with knee function, and whether fatigued strapping tape has the ability to limit ankle range of motion. As the current research has many limitations and inconsistencies, the findings may enable better decision making by practitioners looking to prevent lower limb injuries. This study has been developed with two aims: 1) To inform athletes, and those working with athletes, about the impact of tape fatigue on tapes role as an injury prevention method, and 2) To inform athletes, and those working with athletes, about the impact of ankle tape on knee mechanics.

Interventions

The project will be considering the use of rigid strapping tape applied to the ankle, how it impacts biomechanical function at the ankle and knee, and if ankle and knee function changes as the tape fatigues. For this reason, the intervention will be the application of rigid strapping tape to the ankles of participants. The testing involved will require a single testing session conducted in the Charles Sturt University (Albury) Gait Lab, and will take approximately 30-45 minutes. Prior to atten

The project will be considering the use of rigid strapping tape applied to the ankle, how it impacts biomechanical function at the ankle and knee, and if ankle and knee function changes as the tape fatigues. For this reason, the intervention will be the application of rigid strapping tape to the ankles of participants. The testing involved will require a single testing session conducted in the Charles Sturt University (Albury) Gait Lab, and will take approximately 30-45 minutes. Prior to attending the testing session the participant will have looked over the information form, and completed the Consent Form, the Physical Activity Readiness Questionnaire (PAR-Q), and the Activity and Injury Questionnaire. These will be reviewed on arrival to ensure the potential participant is safe to complete testing. All testing will be carried out by two honours students and one supervisor. The honours students are third year students in the Podiatry undergraduate course. All researchers have current first aid training. The supervisor has both Human Movement and Podiatry undergraduate qualifications, and over 10 years clinical experience. The testing will start with the researchers measuring the participant’s height, weight and hip measurements and lower limb dimensions. At the early stage of testing each participant will be randomly assigned to one of two groups. Group one will have their ankles strapped using rigid strapping tape (Elastoplast woven strapping tape with adhesive backing - 5am width) and a standard strapping technique (combination of anchor, two stirrups, a figure 6 strap, two heel locks, and a second anchor - consistent with that described in the 'Sports Medicine for Sports Trainers' manual - 2007), Group two will not require any strapping tape to be applied. The participant will be asked to wear a chest strap heart rate monitor as one of the fatigue measures during testing. This will be applied prior to mark-up which will allow us to obtain resting heart rate measures. Reflective markers will be placed on the skin of both lower limbs and torso. These markers will allow recording of movement during the dynamic activities with 3D cameras. Using standard, non-invasive procedures, both lower limbs will be prepared and surface electrodes placed on the skin at selected muscle sites. This will allow measurement of muscle activity during the movement tasks. After completing a low intensity 5-minute treadmill warm-up, the participant will be guided through a series of activities which will serve the purpose of the fatigue protocol. These activities will include lateral shuffles, forward/backward running, agility ladder, figure-of-8, forward running with a 45 degree cut task, wall jumps, jumping over cones, and zigzags. The participant will be free to complete the activities at their own pace, although we will ask that they complete the tasks at a high velocity which they find comfortable. The physical tasks will be repeated for 20 minutes. Recording of the 45 degree cut task will occur at 0min, 5min, 10min, 15min and 20min intervals while the fatigue protocol is being completed. Recording will involve 3D motion analysis, as well as the use of EMG (Electromyography), heart rate and ground reaction force. The participant will also be asked to complete a rating of perceived exertion (RPE) at the previously identified time intervals to help gauge fatigue levels. Upon completion the participant will have all markers, sensors and the heart rate monitor removed, and will be offered a guided five minute treadmill cool down and stretching.

Sponsors

Charles Sturt University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

Participants should be: - Between the ages of 18 and 35 - Free of neurovasulcar, vascular or musculoskeletal injury - Not pregnant - Not dependent on medical care

Exclusion criteria

Potential participants will be excluded on the following grounds: - Younger than 18 or older than 35 - Currently experiencing a neurovasulcar, vascular or musculoskeletal injury - Currently pregnant

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026