|dc.identifier.citation||Journal of Education, Health and Sport, Vol. 8, No 9 (2018), s. 1361-1375||pl_PL|
|dc.description.abstract||Aim of the study: The aim of the study was to evaluate the postural stability in a group of patients
with cystic fibrosis.
Material and methods: The study included a group of 44 patients with cystic fibrosis with the
analysis of parameters in the age groups under 16 years (mean 10,1 ± 3,6) and over 16 years (mean
23,6 ± 7,3). For stabilometric measurements, a two-plate CQ Stab posturograph and for body
posture measurements Posturometr-S was used.
Results: The mean value of the SP body balance COP index in the measurement with open eyes
was 336,1 ± 123 mm in the younger group and 201,3 ± 47 mm in the older age group. The results
differed significantly in the measurement with closed eyes in both age groups, similarily to the
other indicators of the balance in the assessment for each planes. The indicators associated with
the assessment of COP displacement significantly correlated negatively with the age of the
subjects, where for the measurement with eyes closed this relationship was the highest in the group
up to 16 years and was r = - 0,90 (p <0,0001) and the size of the chest kyphosis angle ( for the
whole group: r = - 0,45, p = 0,002) and some indicators of the pulmonary system. The correlation
value for FEV1% pred., for the whole group, was r = 0,41 (p = 0,005). It was observed that with
the age of the subjects, the kyphosis angle increased (for the group > 16 years: r = 0,77, p <0,0001).
Conclusions: The results of the study show that with age of the cf patients, changes in the spine
in the sagittal plane, the parameters related to postural stability of the body may be improved.||pl_PL|
|dc.rights||Uznanie autorstwa-Użycie niekomercyjne-Na tych samych warunkach 3.0 Polska||*|
|dc.title||Postural stability in patients with cystic fibrosis||pl_PL|
|Appears in Collections:||Artykuły (WSiNoE)|