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Cervical Kinematics' Reliability: Zero Positioning Using a 3-D-bulls Eye Spirit Level

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02716389
Enrollment
20
Registered
2016-03-23
Start date
2016-03-31
Completion date
2016-04-30
Last updated
2016-04-19

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

Conditions

Cervical, Kinematics, Reliability

Brief summary

The measurement of cervical spine range of motion (ROM) figures among the most common aspects of clinical diagnosis. Good reliability has been demonstrated for assessments using ultrasonic movement analysis systems, such as Zebris CMS 70 (Isny, Germany). However, in contrast to combined measurements of movement amplitudes (e.g., flexion plus extension in the sagittal plane), separating the respective components provides less reliable results. Current research suggest that this is due to the participants' determination of the zero position. This position is influenced by possible disposed treatments and, in particular, by the subject in case of subjective determination. The present study therefore aims to examine the test-retest reliability of separate ROM assessments using a bulls eye spirit meter. Twenty healthy participants will be included in the trial that adopts a two-armed randomized, crossover design. With a washout-period of one week in between, each subject participates in two sessions in a randomised order. In both sessions, cervical ROM (flexion/extension, rotation, lateral flexion) will be measured twice (with a five-minute wait period). In all measurements, the zero position will be determined by means of a bulls eye spirit level. The difference of the two sessions consists in the design of the waiting period. In one session, the subjects will keep the mask carrying the ultrasound markers on their head. In the other session, the mask will be removed during the break.

Interventions

OTHERZebris CMS 70
OTHER3-D Bulls Eye Spirit Meter

Sponsors

Goethe University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Subscribing informed consent * Healthy

Exclusion criteria

* Severe orthopedic, cardiovascular, neurological, psychiatric or endocrine diseases * Not completely healed traumata * Drug intake in the past 48 hours * Pregnancy * Muscle soreness

Design outcomes

Primary

MeasureTime frame
Maximal cervical range of motion in flexion/extension2 min.

Secondary

MeasureTime frame
Maximal cervical range of motion in lateral flexion2 min.
Maximal cervical range of motion in rotation2 min.

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026