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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05752006
Other study ID # SWE_Flexion2_Crane
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 5, 2023
Est. completion date November 15, 2023

Study information

Verified date October 2023
Source University of Primorska
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

An experimental study, which will aim to compare changes of trunk mechanical properties and neuromuscular control following spinal flexion exposure in crane operators and control subjects.


Description:

Our experimental study will include 40 participants, more specifically 15 crane operators and 15 control subjects. All participants will complete a 60-min protocol of intermittent trunk flexion. Measurements of trunk mechanical properties and neuromuscular control will be performed prior to and following the 60-min protocol.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date November 15, 2023
Est. primary completion date October 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 30 Years to 55 Years
Eligibility Inclusion Criteria: - Crane operators: employed as crane operators for more than 3 years - Occupational workers with a predominantly non static job (e.g. combination of sitting and standing) Exclusion Criteria: - History of chronic low back pain - Episode of acute low back pain - Hip injury in the past six months - Previous spine, pelvis or hip surgery - Hypermobility, diagnosed with the Beighton score - High intensity resistance training (> 75 % of 1 repetition maximum) more than two times a week - Control group: sporting or recreational activities, that include repetitive spinal flexion or maintenance of a flexed posture (for example cycling or rowing).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Repeated trunk flexion
A 60-min intermittent trunk flexion protocol. Participants will sit on a standard height sit, with their knees bent at approximately 90° with their hands crossed on their chest. They will perform 40 sets of 60 s of maintaining a flexed position, interspersed with 30 s of rest. Participants will achieve the flexed position by tilting the pelvis posteriorly and leaning forward. During rest, participants will sit up straight without leaning on the support.

Locations

Country Name City State
Slovenia University of Primorska, Faculty of Health Sciences Izola Primorska

Sponsors (1)

Lead Sponsor Collaborator
University of Primorska

Country where clinical trial is conducted

Slovenia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in muscle stiffness Muscle stiffness will be measured using ultrasound-based shear wave elastography during prone lying and forward stooping. Erector spinae and multifidus muscle stiffness will be expressed as the shear modulus value in kilopascals. 90 minutes
Secondary Change in range of motion Trunk flexion range of motion will be evaluated using Spinal Mouse in maximal trunk flexion while standing. 90 minutes
Secondary Change in length of the spine The length of spine will be measured on a custom-developed stadiometer, with the participants in a seated position. 90 minutes
Secondary Change in muscle activity Muscle activity will be measured using electromyography during standing, a forward stoop hold and during maximal trunk flexion. 90 minutes
Secondary Change in lumbar lordosis angle The lumbar lordosis angle will be evaluated using Spinal Mouse during upright standing. 90 minutes
Secondary Change in trunk extension maximal strength Isometric trunk extension peak torque will be assessed on a trunk dynamometer. 90 minutes
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