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The Validity and Reliability of the Four Square Step Test

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信息的提供 (责任方):
Emine Handan Tüzün,Eastern Mediterranean University
October 1, 2018
October 3, 2018
October 3, 2018
October 2018
October 2018   (主要结果测量的最终数据收集日期)
The Four Square Step test[ Time Frame: At baseline ]
Assessing of the dynamic balance in typically developed children. A square will be formed by using four 90 cm long canes placed on the ground. Instructions will be given and encouraged to complete the sequence as fast as possible without touching the canes. The sequence of trial was 1,2,3,4,1,4,3,2,1. The best time will be taken as the score of FSST which are completed successfully.

与当前相同
  • The Time Up and Go test[ Time Frame: At baseline ]
    Assessing of the dynamic balance in typically developed children. A three meter pathway on the testing floor will be marked with red colored masking tape. The TUG will be administered using 2 standard chairs. The best time will be taken as the score of TUG which are completed successfully.
 
The Validity and Reliability of the Four Square Step Test
The Validity and Reliability of the Four Square Step Test in Typically Developed Children

This study will evaluate concurrent and discriminative validity, reliability and level of agreement between the Timed Up & Go test and the four square step test in typically developed children.

Participants will be assessed by two physiotherapists on two separate days. Prior to the trial, testing instructions to be delivered to participants will be translated and adapted into Turkish. In order to maximize potential agreement and to improve rating accuracy, reliability, and validity, assessment skills of the raters will be refreshed through training. Administration of the tests will be performed in a corridor of the school. Assessments will be performed in a quiet and adequately lighted environment to minimize the distraction. Participants will be tested with their regular footwear. The demographic information of participants will be recorded. The dynamic balance performances on the four square step test (FSST) and the Timed up & Go test (TUG) will be assessed by Rater A and B independently and these assessments repeated 24-h later. The participants will be allowed to rest up to five minutes between sessions. A stopwatch will be used to measure time to complete the FSST and TUG test. Evaluations of concurrent and discriminative validity will be based on mean scores from the first measurement of rater A. Pearson's correlation coefficient (r) will be used to assess the concurrent validity of the FSST and TUG tests. Between-groups discriminative validity of the FSST will be evaluated by the one-way analysis of variance (ANOVA) with Bonferroni post-hoc test. Both intra- and inter-rater reliability will be assessed using intraclass correlation coefficients (ICC). ICC2,1 and ICC2,2 estimates and their 95% confidence intervals will be calculated based on absolute-agreement. Bland & Altman plots will be constructed to demonstrate agreement between TUG and FSST, and between assessments of rater A and B.
Observational
分配:
干预模型:
干预模型描述:
盲法: Observational
盲法描述:
主要目的:
  • Diagnostic Test: the Four Square Step test
    A square will be formed by using four 90 cm long canes placed on the ground. The sequence will be explained and demonstrated to the participants. They will be allowed one practice trial and subsequently two trials. Instructions will be given and encouraged to complete the sequence as fast as possible without touching the canes. The sequence of trial was 1,2,3,4,1,4,3,2,1. If a participant touch the canes, or perform the test sequence inaccurately, or both feet of the participant do not make contact with the floor in each square, the trial will be considered as unsuccessful and the test will be repeated. One unsuccessful trial will be allowed. The best time will be taken as the score of FSST which are completed successfully.
  • :
 
Not yet recruiting
150
与当前相同
October 2018
October 2018   (主要结果测量的最终数据收集日期)
Inclusion Criteria: - aged 5 to 10 years, Exclusion Criteria: - have musculoskeletal or neurological disorders, - have history of surgeries of the spine or orthopedic, - have uncorrected visual acuity.
参与研究的性别: All
最小年龄:5 Years ,最大年龄:10 Years  
没有
 
研究美国FDA监管的药品: No
研究涉及美国FDA监管的设备产品: No
计划分享 IPD:
Emine Handan Tüzün,Eastern Mediterranean University
Eastern Mediterranean University
Principal Investigator: Selma Uzuner, MSc.,PT. Eastern Mediterranean University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation,
Principal Investigator: Buse Sezerel, MSc.,PT. Eastern Mediterranean University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation,
Principal Investigator: Hayriye Tomaç, MSc.,PT. Eastern Mediterranean University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation,
Principal Investigator: Serpil Mıhçıoğlu, MSc.,PT. Eastern Mediterranean University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation,
Principal Investigator: Wayne Dite, BAppSci (PE) Austin Hospital Royal Talbot Rehabilitation Center, Kew, Vic, Australia
Eastern Mediterranean University
October 2018

ICMJE     国际医学期刊编辑委员会和 世界卫生组织 ICTRP 要求的元素
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