| Literature DB >> 35400833 |
Kazuya Akiyama1, Shinta Takeuchi2, Yukiko Makihara2, Yusuke Nishida1,2.
Abstract
[Purpose] Spatial attention evaluations are beneficial for patients with unilateral spatial neglect or dementia. Thus, such evaluations are crucial among these patients for determining functional disorder extents. The study aimed to determine minimal detectable changes in reaction time to the Posner task among healthy young participants for establishing spatial attention evaluation protocols. [Participants and Methods] The study recruited 10 healthy young adults (five males and five females; mean age: 28.9 ± 4.0 years). Each participant completed two sessions of the Posner task with 160 trials per session. The reaction time for each trial was measured. Data obtained by the two blocks were analyzed by Bland-Altman analysis, and intraclass correlation coefficient case 1 and minimal detectable changes at the 95% confidence interval were calculated.Entities:
Keywords: Posner task; Reliability; Spatial attention
Year: 2022 PMID: 35400833 PMCID: PMC8989487 DOI: 10.1589/jpts.34.257
Source DB: PubMed Journal: J Phys Ther Sci ISSN: 0915-5287
Fig. 1.The protocols of the Posner task. The central fixation spot (square) and the square boxes located to the left and right of the central fixation were displayed at the beginning of each trial. The boxes were placed at a 3.3° of visual angle to either side of the fixation spot. At the beginning of each trial, a cue arrow pointing to the left or right box was superimposed on the fixation spot for a period of 2,360 ms. Leftward or rightward arrows were equally probable. After a randomly selected Stimulus onset asynchrony (SOA) between 1,500‒3,000 ms, a 100 ms target stimulus (turns red) was flashed in the box. On a valid trial (75% of the trials), a target appeared at the cued location. On an invalid trial (25% of the trials), a target appeared at the uncued location. After detection of the target stimulus or after 4,720 ms from the target stimulus presentation, the next trial was started in an interstimulus interval (ISI) of 1,000 ms. Sessions contained 160 trials, and trial types (valid, invalid) were randomly intermixed.
Results of the reaction time (in ms), Blamd–Altman analysis, ICC case 1, and MDC95 (in ms) under each condition
| Bland–Altman analysis | ICC (1,1) | MDC95 | |||||
| Reaction time | |||||||
| (mean ± SD) | Fixed bias | Proportional bias | |||||
| Block 1 | Block 2 | 95% confidence interval | Slope of the regression of differences | ||||
| Valid trial (right) | 337 ± 27 | 334 ± 27 | −6.17–12.01 | 0.04 | p=0.91 | 0.91 | 24 |
| Valid trial (left) | 340 ± 28 | 338 ± 26 | −6.63–10.79 | 0.20 | p=0.57 | 0.91 | 23 |
| Invalid trial (right) | 352 ± 30 | 349 ± 26 | −8.07–14.51 | 0.27 | p=0.45 | 0.87 | 29 |
| Invalid trial (left) | 357 ± 33 | 350 ± 31 | −5.92–19.89 | 0.12 | p=0.74 | 0.85 | 34 |
ICC: intraclass correlation coefficients; MDC95: minimal detectable change at 95% confidence interval.
Fig. 2.Bland–Altman plot of each condition. For Bland–Altman analysis, the 95% CI for the mean difference included 0, and the slope of the regression of mean differences was not significant in all conditions.