scholarly journals Validity and Reliability of the GymAware Linear Position Transducer for Squat Jump and Counter-Movement Jump Height

Sports ◽  
2018 ◽  
Vol 6 (4) ◽  
pp. 177 ◽  
Author(s):  
Tanuj Wadhi ◽  
Jacob Rauch ◽  
Nauris Tamulevicius ◽  
Jody Andersen ◽  
Eduardo De Souza
Keyword(s):  
Test Validity ◽  
Jump Height ◽  
Altman Analysis ◽  
Squat Jump ◽  
Retest Reliability ◽  
Bland Altman Analysis ◽  
Position Transducer ◽  
Counter Movement Jump ◽  
Significant Difference ◽  
Test Retest Reliability

The purpose of this study was to assess the concurrent validity and test-retest reliability of a linear position transducer (LPT) for the squat jump (SJ) and counter-movement jump (CMJ) height. Twenty-eight subjects (25.18 ± 7.1 years) performed three SJs followed by three CMJs using a force plate concurrently with the LPT to test validity. Subjects returned on a separate day, at least 48 h apart, to measure test-retest reliability. A t-test showed a significant difference between the two devices for both SJ (p < 0.001) and CMJ (p < 0.001) while Bland–Altman analysis for validity revealed that the LPT overestimated jump height for both SJ (mean difference (MD) = 8.01 ± 2.93 cm) and CMJ (MD = 8.68 ± 2.99 cm). With regards to reliability of the LPT, mean intraclass correlation (ICC) for both SJ (ICC = 0.84) and CMJ (ICC = 0.95) were high, and Bland–Altman analysis showed mean differences lower than minimal detectable change (MDC) between the days for both SJ (MD = 1.89 ± 4.16 cm vs. MDC = 2.72 cm) and CMJ (MD = 0.47 ± 3.23 cm vs. MDC = 2.11 cm). Additionally, there was a low coefficient of variation (CV) between days for both SJ (CV = 3.25%) and CMJ (CV = 0.74%). Therefore, while the LPT overestimates jump height, it is a reliable tool for tracking changes in jump height to measure performance improvement and monitor fatigue.

scholarly journals Test–Retest Reliability of a Conventional Gait Model for Registering Joint Angles during Initial Contact and Toe-Off in Healthy Subjects

2021 ◽  
Vol 18 (3) ◽  
pp. 1343
Author(s):  
Francisco Molina-Rueda ◽  
Pilar Fernández-González ◽  
Alicia Cuesta-Gómez ◽  
Aikaterini Koutsou ◽  
María Carratalá-Tejada ◽  
...  
Keyword(s):  
Healthy Subjects ◽  
Intraclass Correlation ◽  
Minimal Detectable Change ◽  
Initial Contact ◽  
Altman Analysis ◽  
Joint Angles ◽  
Retest Reliability ◽  
Bland Altman Analysis ◽  
Motion System ◽  
Test Retest Reliability

The aim of this study was to evaluate the test–retest reliability of a conventional gait model (CGM), the Plug-in Gait model, to calculate the angles of the hip, knee, and ankle during initial contact (IC) and toe-off (TO). Gait analysis was performed using the Vicon Motion System® (Oxford Metrics, Oxford, UK). The study group consisted of 50 healthy subjects. To evaluate the test–retest reliability, the intraclass correlation coefficient (ICC), the standard error of measurement (SEM), the minimal detectable change (MDC), and the Bland–Altman analysis with 95% limits of agreement were calculated. The ICC for the joint angles of the hip, knee, and ankle was higher than 0.80. However, the ankle angle at IC had an ICC lower than 0.80. The SEM was <5° for all parameters. The MDC was large (>5°) for the hip angle at IC. The Bland–Altman analysis indicated that the magnitude of divergence was between ±5° and ±9° at IC and around ±7° at TO. In conclusion, the ICC for the plug-in gait model was good for the hip, knee, and ankle angles during IC and TO. The plots revealed a disagreement between measurements that should be considered in patients’ clinical assessments.

scholarly journals Can EOS imaging substitute traditional AP pelvis radiographs? A Comparative study

2020 ◽  
Vol 8 (4_suppl3) ◽  
pp. 2325967120S0026
Author(s):  
Jenna Powell ◽  
Romie Gibly ◽  
Wade Faulk ◽  
Stephanie Watson Mayer ◽  
Courtney Michelle O’Donnell
Keyword(s):  
Imaging System ◽  
Intraclass Correlation ◽  
Young Patients ◽  
Altman Analysis ◽  
Retest Reliability ◽  
Bland Altman Analysis ◽  
Center Edge ◽  
Eos Imaging ◽  
Acetabular Morphology ◽  
Test Retest Reliability

INTRODUCTION: Young patients followed for hip disorders often require serial imaging and incur significant radiation to the abdomen and pelvis. The EOS imaging system offers a low-radiation alternative. However, consistency with radiographic parameters from conventional radiographs (CR) have not been studied. We evaluated the reliability and validity of EOS imaging in comparison to CR in evaluating acetabular morphology. METHODS: 48 hips (27 patients, 66.67% female, 14.4 ± 3.6 years old), indicated for open hip preservation procedure between 2015-2017, which had both EOS imaging and AP pelvis CR taken pre-operatively were examined. Both symptomatic and contralateral hips were measured, excluding hips with prior osteotomies. Three orthopaedic surgeons measured Tonnis angle, lateral center edge angle (LCEA), acetabular depth ratio (ADR), and extrusion index (EI) in both imaging modalities. Images were measured twice, two weeks apart. Reliability was assessed using intraclass correlation coefficients (ICC). Bland-Altman analysis was used to evaluate test-retest agreement and inter-modality agreement. RESULTS: Test-retest reliability was excellent for all raters on all tests (ICC range 0.8047 to 0.9714). Inter-rater reliability was also excellent for all measures on both modalities (ICC range 0.8593 to 0.9547). ICC values were consistent across EOS and CR. By Bland-Altman analysis, test-retest agreement was high, with no statistically significant mean differences in any test or modality (p > 0.6) except LCEA measured on EOS images (p = 0.02), which was 1.16° lower. Tonnis angle (p < 0.005) and ADR (p < 0.001) were statistically different from EOS to CR. Bias was also not uni-directional across tests: LCEA and ADR were, on average, higher on CR while Tonnis angle and EI were, on average, higher on EOS images. Reliability between the EOS and CR images was excellent for all raters on all tests (ICC range 0.8402 to 0.9458). DISCUSSION AND CONCLUSION: LCEA, ADR, EI, and Tonnis angle have consistently high test-retest reliability, test-retest agreement, and inter-observer reliability in both EOS imaging and CR to evaluate acetabular morphology. Inter-modality disagreement was observed between EOS and CR, but the difference was small and likely not clinically significant. When establishing acetabular morphology, these results suggest that EOS may provide an opportunity to minimize radiation exposure for patients followed long-term for hip pathology while maintaining the accuracy of diagnostic measures. [Table: see text][Table: see text]

scholarly journals The Development of a Paediatric Phoneme Discrimination Test for Arabic Phonemic Contrasts

2021 ◽  
Vol 11 (2) ◽  
pp. 150-166
Author(s):  
Hanin Rayes ◽  
Ghada Al-Malky ◽  
Deborah Vickers
Keyword(s):  
Closed Set ◽  
Retest Reliability ◽  
Response Options ◽  
Phoneme Discrimination ◽  
Significant Difference ◽  
Age Appropriate ◽  
Hearing Children ◽  
Test Retest Reliability ◽  
Development And Validation ◽  
Arabic Speaking

Objective: The aim of this project was to develop the Arabic CAPT (A-CAPT), a Standard Arabic version of the CHEAR auditory perception test (CAPT) that assesses consonant perception ability in children. Method: This closed-set test was evaluated with normal-hearing children aged 5 to 11 years. Development and validation of the speech materials were accomplished in two experimental phases. Twenty-six children participated in phase I, where the test materials were piloted to ensure that the selected words were age appropriate and that the form of Arabic used was familiar to the children. Sixteen children participated in phase II where test–retest reliability, age effects, and critical differences were measured. A computerized implementation was used to present stimuli and collect responses. Children selected one of four response options displayed on a screen for each trial. Results: Two lists of 32 words were developed with two levels of difficulty, easy and hard. Assessment of test–retest reliability for the final version of the lists showed a strong agreement. A within-subject ANOVA showed no significant difference between test and retest sessions. Performance improved with increasing age. Critical difference values were similar to the British English version of the CAPT. Conclusions: The A-CAPT is an appropriate speech perception test for assessing Arabic-speaking children as young as 5 years old. This test can reliably assess consonant perception ability and monitor changes over time or after an intervention.

Validity and reliability of the Turkish version of the Patient Dignity Inventory

2021 ◽  
pp. 1-8
Author(s):  
Yasemin Eskigülek ◽  
Sultan Kav
Keyword(s):  
Palliative Care ◽  
Factor Analysis ◽  
Intraclass Correlation ◽  
Validity And Reliability ◽  
Turkish Version ◽  
Retest Reliability ◽  
Significant Difference ◽  
Test Retest Reliability ◽  
Fit Index ◽  
Turkish Society

Abstract Objective The aim of this study was to investigate the validity and reliability of the Patient Dignity Inventory (PDI) in the Turkish society, which was developed to evaluate dignity-related distress in palliative care patients. Methods One hundred and twenty-seven adults with advanced cancer hospitalized in several clinics of two university hospitals were included in the study. The patients whose Palliative Performance Scale score was at least 40% were recruited to study. The data were collected with a patient demographic form, the Turkish version of Hospital Anxiety and Depression Scale (HADS-TR), and the Turkish version of the PDI (PDI-TR). The PDI-TR was finalized and back-translated after translating into Turkish and obtaining 10 expert opinions. Exploratory and confirmatory factor analysis, internal consistency, concurrent validity, and test–retest reliability analysis were performed. Results The Cronbach's α coefficient of PDI-TR was 0.94. Factor analysis resulted in a five-factor solution, and all items were loaded on factors. Factors were labeled as symptom distress, existential distress, self-confidence, dependency, and supportive care needs and accounted for 68.70% of the overall variance. The model's normed fit index, comparative fit index, and X2/SD were found between acceptable range (0.90, 0.93, and 2.64, respectively). A positive and strong correlation was found between subdimension scores of HADS-TR and the total score of PDI-TR (r = 0.70 for anxiety subdimension; r = 0.73 for depression subdimension). The test–retest reliability was conducted with 32 patients within the sample two weeks after the first application, and no significant difference was found between the two application scores as the result of paired-sample t-test (p > 0.05). An intraclass correlation coefficient of test–retest reliability was r = 0.855. Significance of results PDI-TR was found to be a valid and reliable tool in palliative care patients in Turkish society.

scholarly journals Comparison of IOP Measurement by Goldmann Applanation Tonometer, ICare Rebound Tonometer, and Tono-Pen in Keratoconus Patients after MyoRing Implantation

2019 ◽  
Vol 2019 ◽  
pp. 1-7
Author(s):  
Mahmoud Rateb ◽  
Mahmoud Abdel-Radi ◽  
Zeiad Eldaly ◽  
Mohamed Nagy Elmohamady ◽  
Asaad Noor El Din
Keyword(s):  
Central Corneal Thickness ◽  
Pearson Correlation ◽  
Corneal Thickness ◽  
Altman Analysis ◽  
Bland Altman Analysis ◽  
Rebound Tonometer ◽  
Goldmann Applanation Tonometer ◽  
Significant Difference ◽  
Applanation Tonometer ◽  
Icare Rebound Tonometer

Purpose. To evaluate the different IOP readings by Goldmann applanation tonometer (GAT), ICare rebound tonometer, and Tono-Pen in keratoconus patients after MyoRing implantation. To assess the influence of central corneal thickness (CCT) and thinnest corneal location (TCL) on IOP measurements by different tonometers. Setting. Prospective observational study was conducted in two private centers in Egypt from February 2015 to November 2016. Methods. Seventeen eyes of 10 patients suffering from keratoconus and who underwent MyoRing implantation were recruited. All subjects underwent GAT, ICare, and Tono-Pen IOP measurements in random order. Central corneal thickness and thinnest corneal location were assessed by Pentacam. Difference in mean in IOP readings was assessed by T-test. Correlation between each pair of devices was evaluated by Pearson correlation coefficient. The Bland–Altman analysis was used to assess intertonometer agreement. Results. Seventeen eyes (10 patients) were evaluated. The mean IOP reading was 13.9 ± 3.68, 12.41 ± 2.87, and 14.29 ± 1.31 mmHg in GAT, ICare, and Tono-Pen group, respectively. There was a significant difference between IOP readings by GAT/ICare and Tono-Pen/ICare (p value: 0.032 and 0.002, respectively) with no significant difference between GAT/Tono-Pen (p value: 0.554). Mean difference in IOP measurements between GAT/ICare was 1.49 ± 2.61 mmHg, Tono-Pen/ICare was 1.89 ± 2.15 mmHg, and GAT/Tono-Pen was −0.39 ± 2.59 mmHg. There was no significant correlation between the difference in IOP readings among any pair of devices and CCC or TCL. The Bland–Altman analysis showed a reasonable agreement between any pair of tonometers.

scholarly journals Computerized Symbol Digit Modalities Test in a Swiss Pediatric Cohort Part 1: Validation

2021 ◽  
Vol 12 ◽  
Author(s):  
Céline Hochstrasser ◽  
Sarah Rieder ◽  
Ursina Jufer-Riedi ◽  
Marie-Noëlle Klein ◽  
Anthony Feinstein ◽  
...  
Keyword(s):  
High Reliability ◽  
Age Groups ◽  
Reliable Change Index ◽  
Information Processing Speed ◽  
Retest Reliability ◽  
Norm Values ◽  
Significant Difference ◽  
Test Retest Reliability ◽  
The University ◽  
Mean Time

ObjectiveThe objective of this study was to validate the computerized Symbol Digit Modalities Test (c-SDMT) in a Swiss pediatric cohort, in comparing the Swiss sample to the Canadian norms. Secondly, we evaluated sex effects, age-effects, and test–retest reliability of the c-SDMT in comparison to values obtained for the paper and pencil version of the Symbol Digit Modalities Test (SDMT).MethodsThis longitudinal observational study was conducted in a single-center setting at the University Children’s Hospital of Bern. Our cohort consisted of 86 children (45 male and 41 female) aged from 8 to 16 years. The cohort included both healthy participants (n = 38) and patients (n = 48) hospitalized for a non-neurological disease. Forty eight participants were assessed during two testing sessions with the SDMT and the c-SDMT.ResultsTest–retest reliability was high in both tests (SDMT: ICC = 0.89, c-SDMT: ICC = 0.90). A reliable change index was calculated for the SDMT (RCIp = −3.18, 14.01) and the c-SDMT (RCIp = −5.45, 1.46) corrected for practice effects. While a significant age effect on information processing speed was observed, no such effect was found for sex. When data on the c-SDMT performance of the Swiss cohort was compared with that from a Canadian cohort, no significant difference was found for the mean time per trial in any age group. Norm values for age groups between 8 and 16 years in the Swiss cohort were established.ConclusionNorms for the c-SDMT between the Swiss and the Canadian cohort were comparable. The c-SDMT is a valid alternative to the SDMT. It is a feasible and easy to administer bedside tool due to high reliability and the lack of motor demands.

scholarly journals Measuring the occupational balance of people with insomnia in a Chinese population: Preliminary psychometric evidence on the Chinese version of the Occupational Balance Questionnaire

2020 ◽  
pp. 156918612094453
Author(s):  
Eris CM Ho ◽  
Mona Dür ◽  
Tanja Stamm ◽  
Andrew MH Siu
Keyword(s):  
Factor Analysis ◽  
Internal Consistency ◽  
Convergent Validity ◽  
Well Being ◽  
Living Environment ◽  
Chinese Version ◽  
Retest Reliability ◽  
Significant Difference ◽  
Test Retest Reliability ◽  
Insomnia Severity

Background Occupational balance, a fundamental concept in occupational therapy, is the arrangement of right amount and variety of occupations contributes to a person’s health and well-being. This study was aimed to investigate the reliability and validity of the Chinese version of the Occupational Balance Questionnaire (OB-Quest) for people with insomnia. Methods The OB-Quest was translated into traditional Chinese and reviewed by an expert panel for content validity, cultural relevance and translation accuracy. Internal consistency, factor analysis and convergent validity, as well as test–retest reliability, were explored. Results The participants (n = 205), 115 adults with insomnia and 90 adults without insomnia, completed a survey of demographic background, the Chinese version of OB-Quest and the Chinese Insomnia Severity Index (C-ISI). The Chinese version of OB-Quest demonstrated excellent test–retest reliability (ICC= 0.98) and good internal consistency (Cronbach’s α  =  0.80). Factor analysis indicated that a single-factor solution explained 42% of the variance, and 9 out of 10 items had a factor loading of 0.4 or above. The Chinese version of OB-Quest had significant correlations with C-ISI (r = –0.88; p < 0.001). A significant difference was found in occupational balance between groups with different levels of insomnia severity and without insomnia (F = 169.72; p < 0.001). As in a previous study, age, living environment and life role had no significant relationship with occupational balance. Conclusion The Chinese version of OB-Quest is a short, easy to understand and culturally relevant assessment for Chinese. It demonstrates satisfactory psychometric properties and had significant correlations with insomnia.

scholarly journals Comparison of two different optical coherence tomography angiography devices in detecting healthy versus glaucomatous eyes – an observational cross-sectional study

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
A. R. Kee ◽  
V. C. H. Yip ◽  
E. L. T. Tay ◽  
C. W. Lim ◽  
J. Cheng ◽  
...  
Keyword(s):  
Optical Coherence Tomography ◽  
Diagnostic Accuracy ◽  
Optic Disc ◽  
Optical Coherence Tomography Angiography ◽  
Optical Coherence ◽  
Cross Sectional ◽  
Swept Source ◽  
Retest Reliability ◽  
Significant Difference ◽  
Test Retest Reliability

Abstract Background To understand the differences between two different optical coherence tomography angiography (OCTA) devices in detecting glaucomatous from healthy eyes by comparing their vascular parameters, diagnostic accuracy and test-retest reliability. Methods A cross-sectional observational study was performed on healthy and glaucoma subjects, on whom two sets of OCTA images of optic disc and macula were acquired using both AngioVue (Optovue, USA) and Swept Source (Topcon, Japan) OCTA devices during one visit. A novel in-house software was used to calculate the vessel densities. Diagnostic accuracy of the machines in differentiating healthy versus glaucomatous eyes was determined using area under the receiver operating characteristic curve (AUROC) and test-retest repeatability of the machines was also evaluated. Results A total of 80 healthy and 38 glaucomatous eyes were evaluated. Glaucomatous eyes had reduced mean vessel density compared to healthy controls in all segmented layers of the optic disc and macula using AngioVue (p ≤ 0.001). However, glaucomatous eyes had higher mean vessel density on optic disc scans using Swept Source, with lack of statistically significant difference between healthy and glaucomatous eyes. The AUROC showed better diagnostic accuracy of AngioVue (0.761–1.000) compared to Swept Source (0.113–0.644). The test-retest reliability indices were generally better using AngioVue than Swept Source. Conclusions AngioVue showed better diagnostic capability and test-retest reliability compared to Swept Source. Further studies need to be undertaken to evaluate if there is any significant difference between the various machines in diagnosing and monitoring glaucoma.

scholarly journals Test-Retest Reliability of a Commercial Linear Position Transducer (GymAware PowerTool) to Measure Velocity and Power in the Back Squat and Bench Press

2020 ◽  
Vol 34 (3) ◽  
pp. 728-737 ◽  
Author(s):  
Samuel T. Orange ◽  
James W. Metcalfe ◽  
Phil Marshall ◽  
Rebecca V. Vince ◽  
Leigh A. Madden ◽  
...  
Keyword(s):  
Bench Press ◽  
Retest Reliability ◽  
Position Transducer ◽  
Back Squat ◽  
Test Retest Reliability

scholarly journals Concurrent Validity and Reliability of My Jump 2 App for Measuring Vertical Jump Height in Recreationally Active Adults

2020 ◽  
Vol 10 (11) ◽  
pp. 3805 ◽  
Author(s):  
Špela Bogataj ◽  
Maja Pajek ◽  
Slobodan Andrašić ◽  
Nebojša Trajković
Keyword(s):  
Concurrent Validity ◽  
Female Athletes ◽  
Vertical Jump ◽  
Intraclass Correlation ◽  
Jump Height ◽  
Validity And Reliability ◽  
Retest Reliability ◽  
Study Results ◽  
Test Retest Reliability ◽  
Active Adults

This study aimed to examine the reliability, validity, and usefulness of the smartphone-based application, My Jump 2, against Optojump in recreationally active adults. Participants (18 women, 28.9 ± 5.6 years, and 26 men, 30.1 ± 10.6 years) completed squat jumps (SJ), counter-movement jumps (CMJ), and CMJ with arm swing (CMJAS) on Optojump and were simultaneously recorded using My Jump 2. To evaluate concurrent validity, jump height, calculated from flight time attained from each device, was compared for each jump type. Test-retest reliability was determined by replicating data analysis of My Jump 2 recordings on two occasions separated by two weeks. High test-retest reliability (Intraclass correlation coefficient (ICC) > 0.93) was observed for all measures in both male and female athletes. Very large correlations were observed between the My Jump 2 app and Optojump for SJ (r = 0.95, p = 0.001), CMJ (r = 0.98, p = 0.001), and CMJAS (r = 0.98, p = 0.001) in male athletes. Similar results were obtained for female recreational athletes for all jumps (r > 0.94, p = 0.001). The study results suggest that My Jump 2 is a valid, reliable, and useful tool for measuring vertical jump in recreationally active adults. Therefore, due to its simplicity and practicality, it can be used by practitioners, coaches, and recreationally-active adults to measure vertical jump performance with a simple test as SJ, CMJ, and CMJAS.

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