Reliability and Validity of a New Ankle Dorsiflexion Lunge Test Using a Level Laser.

Sponsor
University of Bologna (Other)
Overall Status
Recruiting
CT.gov ID
NCT05403892
Collaborator
(none)
50
1
2.1
23.8

Study Details

Study Description

Brief Summary

The study aims to find validity and intra-inter examiner reliability of the Lever Laser Lunge Test (LLLT). This is a new way to measure ankle range of motion during weight bearing, instead of classical dorsiflexion lunge test The study wants to assume that LLLT is comparable to the traditional test but more efficient because it could be used in different settings.

To reach this goal, these two non-invasive tests will be performed to measure the amount of movement of the ankle joint in healthy teenage basketball players.

Data will be statistically compared and studied.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: level laser lunge test
  • Diagnostic Test: dorsiflexion Lunge test

Detailed Description

The dorsiflexion lunge test or knee-to-wall test (DLT) measure the range of movement of weight bearing ankle dorsiflexion. This test is frequently used in sport setting, in order to identify ankle limitations which could lead to possible injuries or joint overloads.

DLT is a cheap and simple measurement method to assess the ankle dorsiflexion, however clinicians find possible bias that reduce the usability of this test.

In order to remove this bias, this study suggests a new measurement method carried out by a level laser to create a virtual wall (the vertical red line produced by the laser).

The study aims therefore to estimate the validity and intra-inter examiner reliability of this method, in comparison to the DLT.

The instruments used are a professional level laser and a rigid ruler. A group of male teenager basketball players from Bologna competitive sports clubs will be recruited.

In order to assess the validity of this new test the clinicians will compare statistically the outcome of both test In order to assess the intra and inter examiner reliability the clinicians will compare repeated measurements of the LLLT.

It is assumed that both measurement methods (traditional and laser method) have comparable validity but LLLT reliability intra and inter examiner should be higher than the DLT one.

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Inter and Intra-observer Reliability and Validity of the Ankle Dorsiflexion Lunge Test With a Level Laser in Healthy Teenage Athletes: a Novel Way of Measuring.
Actual Study Start Date :
May 28, 2022
Anticipated Primary Completion Date :
Jun 30, 2022
Anticipated Study Completion Date :
Jul 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Participant

The participants must be teenage basketball players (12-17 years old). The exclusion criteria are: have suffered in the last 3 months of lower limb musculoskeletal disorders such as pain for more than 7 days (ankle distortion outcomes, leg/foot fractures, plantar heel pain, metatarsalgias, etc); athletes who have undergone surgery on their lower limb.

Diagnostic Test: level laser lunge test
In order to perform the Level Laser Test, the operator 1 places a laser lever on the ground one metre aside and 50 cm forward the ankle to be examined. This laser (a 2-class laser not harmful to the eyes) maintains a linear laser light beam perpendicular to the floor. The examined leg is placed further forward to the other one, as it happens in the DLT. The teenage performs a forward lunge perpendicularly to the laser line, the heel positioning 50 cm from the laser line. Operator 1 has the subject perform a lunge while operator 2 measures the distance from the kneecap to the laser line. The measurement, deducted by 50 cm, leads to the heel-to-wall distance (value used to DLT).

Diagnostic Test: dorsiflexion Lunge test
The dorsiflexion lunge test (DLT) will be used to measure ankle dorsiflexion. To perform this test, the teenage stands in front of a wall holding the foot of their limb to be measured perpendicularly to it. The other foot is to be kept behind it. The teenage is asked to perform a lunge (to dorsiflex the ankle and bring the knee into flexion) until the front knee touches the wall without the heel lifting off the ground. The teenage steps away from the wall as much as possible as long as the knee keeps touching the wall. Measurement in centimeters is taken from the heel of the examined leg to the wall.
Other Names:
  • weight bearing lunge test
  • Outcome Measures

    Primary Outcome Measures

    1. validity of lever laser lunge test [1 day]

      the collected values will be statistically processed to identify a significant validity of the LLLT comparing to the DLT

    2. intra-examiner reliability of lever laser lunge test [2 days]

      the collected values will be statistically processed to identify a significant intra-examiner reliability of the LLLT compared to the DLT values found in the bibliography

    3. inter-examiner reliability of lever laser lunge test [2 days]

      the collected values will be statistically processed to identify a significant inter-examiner reliability of the LLLT compared to the DLT values found in the bibliography

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    12 Years to 17 Years
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • male teenagers basketball players enrolled in a competitive sports club;

    • teenagers whose parents have signed the privacy and consent forms.

    Exclusion Criteria:
    • athletes who have suffered in the last 3 months of lower limb musculoskeletal disorders such as pain for more than 7 days (ankle distortion outcomes, leg/foot fractures, plantar heel pain, metatarsalgias, etc);

    • athletes who have undergone surgery on their lower limb.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Dipartimento di Scienze Biomediche e Neuromotorie (DIBINEM) Bologna Italy 40138

    Sponsors and Collaborators

    • University of Bologna

    Investigators

    • Principal Investigator: Tommaso Torriglia, Università degli studi di Bologna
    • Study Director: Pillastrini Paolo, Università degli studi di Bologna
    • Study Chair: Silvia Pozzan, Università degli studi di Bologna

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Ballardin Francesco, Clinical Professor, University of Bologna
    ClinicalTrials.gov Identifier:
    NCT05403892
    Other Study ID Numbers:
    • TMUNIBO2022TT
    First Posted:
    Jun 3, 2022
    Last Update Posted:
    Jun 13, 2022
    Last Verified:
    Jun 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Ballardin Francesco, Clinical Professor, University of Bologna

    Study Results

    No Results Posted as of Jun 13, 2022