Correll Sarah, Field Jennifer, Hutchinson Heather, Mickevicius Gabby, Fitzsimmons Amber, Smoot Betty
Breakthrough Physical Therapy, Sunnyvale, CA, USA.
Kaiser Permanente Vallejo, Vallejo, CA, USA.
Int J Sports Phys Ther. 2018 Aug;13(4):707-714.
Range of motion (ROM) of the shoulder is an integral component of assessment of musculoskeletal shoulder impairments. ROM is typically measured using a universal goniometer (UG). The UG has demonstrated good intra and inter-rater reliability for measuring shoulder ROM, although limitations exist. In recent years, alternative measurement devices such as smartphone applications and digital goniometers have been introduced, potentially addressing some of the shortcomings of the UG. Limited research is available on the validity and reliability of these alternative devices, including the laser-guided digital goniometer, in measuring shoulder ROM.Purpose: The purpose of this study was to investigate the intra- and inter-rater reliability and concurrent validity of a laser-guided digital goniometer (HALO) for measuring active shoulder ROM.
A convenience sample of healthy volunteers was recruited. To be eligible, participants were required to be between 18 and 75 years of age and able to actively move at least one shoulder into 90 ° of glenohumeral abduction. Self-report of previous significant shoulder injury; previous shoulder surgery; current bilateral shoulder pain; current neck or upper back pain; or referred pain into the upper extremity were exclusion criteria. Active shoulder flexion, abduction, internal rotation, and external rotation were measured for each shoulder. Two evaluators measured each motion twice with each device (HALO and the UG) per shoulder. The intra-class correlation coefficient (ICC) for reliability and validity/agreement between devices was calculated using a two-way mixed model with a 95% confidence interval.
Data were analyzed for 75 shoulders from 41 participants (seven participants had only one shoulder evaluated). Intra-rater reliability ICCs are between 0.82 and 0.91 for the HALO, and 0.83 to 0.95 for the UG. Inter-rater reliability for the HALO was 0.89 to 0.98 and for the UG was 0.90 to 0.98. The ICCs for agreement, comparing the HALO digital goniometer to the UG ranged from 0.79 to 0.99.
This study provides evidence that the HALO digital goniometer can be a reliable and valid tool for measuring shoulder ROM in individuals with healthy shoulders. However, the two devices should not be used interchangeably to evaluate a single individual's change over time for any motion.
Diagnostic Study (clinical measurement), Level 2b.
肩部活动范围(ROM)是评估肩部肌肉骨骼损伤的一个重要组成部分。ROM通常使用通用角度计(UG)进行测量。尽管存在局限性,但UG在测量肩部ROM方面已显示出良好的评分者内和评分者间信度。近年来,已引入了诸如智能手机应用程序和数字角度计等替代测量设备,可能解决了UG的一些缺点。关于这些替代设备,包括激光引导数字角度计,在测量肩部ROM方面的有效性和可靠性的研究有限。
本研究的目的是调查激光引导数字角度计(HALO)在测量主动肩部ROM方面的评分者内和评分者间信度以及同时效度。
招募了健康志愿者的便利样本。符合条件的参与者年龄需在18至75岁之间,并且能够主动将至少一侧肩部外展至90°。排除标准包括既往有明显肩部损伤的自我报告;既往肩部手术史;当前双侧肩部疼痛;当前颈部或上背部疼痛;或上肢牵涉痛。对每个肩部测量主动肩部前屈、外展、内旋和外旋。两名评估者使用每种设备(HALO和UG)对每个肩部的每个动作测量两次。使用具有95%置信区间的双向混合模型计算设备之间信度和效度/一致性的组内相关系数(ICC)。
对41名参与者的75个肩部的数据进行了分析(7名参与者仅评估了一侧肩部)。HALO的评分者内信度ICC在0.82至0.91之间,UG的评分者内信度ICC在0.83至0.95之间。HALO的评分者间信度为0.89至0.98,UG的评分者间信度为0.90至0.98。将HALO数字角度计与UG进行比较的一致性ICC范围为0.79至0.99。
本研究提供了证据表明,HALO数字角度计可以是测量健康肩部个体肩部ROM的可靠且有效的工具。然而,这两种设备不应互换使用以评估单个个体随时间的任何动作变化。
诊断性研究(临床测量),2b级。