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Does controlling force and orientation when using real time ultrasound imaging improve reliability of measuring transverse abdominis in experienced and novice clinicians?

Reliability of muscle measurement using real time ultrasound imaging in healthy individuals: Comparison of examiner experience to measure transverse abdominis with and without force and orientation control

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616001340426
Enrollment
34
Registered
2016-09-26
Start date
2016-10-21
Completion date
2017-02-22
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

The purpose of the study is to determine if using a standardized method of RTUI improves reliability of measuring the thickness and activation of a muscle in the abdomen (transverse abdominis). The standardized method uses a device that controls for the force and orientation of the US probe. Reliability will be compared in an experienced an an inexperienced examiner. Currently, the reliability of this measure is based mainly on poor quality studies and much of the research does not look at muscle activation. Dysfunction of this muscle has been observed in patients with low back pain, thus their ability to activate is clinically relevant. It is hypothesized that both inter- and intra-rater reliability will be significantly increased when force and orientation of the probe is controlled. Secondly, it is hypothesized that a significantly greater increase in intra-rater reliability will be observed with an inexperienced clinician using this device.

Interventions

The thickness and activation of patient's transverse abdominis (TrA) will be measured using real time ultrasound imaging (RTUI) and the reliability of these measures examined. This will be measured using a device that controls for the force and orientation of the probe (force probe device). The force probe device measures the force, inclination and roll of the US probe and displays these values on a laptop screen. The examiner can then increase/decrease the force applied through the probe to mai

The thickness and activation of patient's transverse abdominis (TrA) will be measured using real time ultrasound imaging (RTUI) and the reliability of these measures examined. This will be measured using a device that controls for the force and orientation of the probe (force probe device). The force probe device measures the force, inclination and roll of the US probe and displays these values on a laptop screen. The examiner can then increase/decrease the force applied through the probe to maintain a consistent amount of pressure. Images are later collected from video files at time points in which the force, inclination and roll match. Data collection will be conducted by both an experienced and an inexperienced examiner. The experienced examiner is a physiotherapist with 23 years clinical experience, a level 2 postgraduate RTUI certificate, 6 years experience in measurement using musculoskeletal RTUI (last 5 measuring TrA and LM). The inexperienced examiner is a fourth year physiotherapy student with 6 hours of training and hands on practice in using RTUI to measure TrA using the force probe device with the experienced examiner and another student who previously completed his honours project using the same equipment. 2-3 sessions of free practice are also planned. Participants will be taught to contract their TrA prior to data collection. Participants will be required to remove their shirt and may be required to lower their pants to expose the top of the pelvis for TrA. Participants will lie on their back with their hips and knees bent to measure TrA. An adhesive tape marker will be used to mark where the ultrasound probe will sit. Videos will be collected using RTUI in movie mode for later analysis. Two videos will be taken of each muscle using the force probe device: a video with the muscle at rest for approximately 20 seconds and a video in which the participant contracts the muscle twice will be captured. The participant will then have the same videos captured again to determine reliability of measurement.

Sponsors

James Cook University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Primary purpose
Educational / counselling / training

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

General population

Exclusion criteria

History of low back pain in the previous 2 years of significant enough severity to seek treatment, unable to tolerate lying on back 30 mins each, pregnancy in past 12 months, allergies to adhesive tapes

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026