Evidence map›Paper›PMID 41793435›Full record

ArticleEuropean journal of applied physiology2026

Peripheral muscle oxygenation during upper extremity functional exercise and balance in pediatric patients with cystic fibrosis: a cross-sectional study.

Betül Yoleri, Meral Boşnak Güçlü, Tuğba Şişmanlar Eyüboğlu, Ayşe Tana Aslan

Registry-linked trialAbstract read
In one paragraph

Article in European journal of applied physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07770854 (Machine Learning Prediction of Pulmonary Function in Children With Cystic Fibrosis), which is not on this map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07770854 completednot on this map

Machine Learning Prediction of Pulmonary Function in Children With Cystic Fibrosis: Multidimensional Analysis of Peripheral Muscle Oxygenation, Postural Balance, and Clinical-Functional Markers

TypeobservationalSponsorGazi UniversityRan2021 to 2025Enrolled31ConditionsCystic Fibrosis (CF)ArmsArchived Multidimensional Clinical and Functional Assessment Data
3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Betül YoleriFaculty of Health Sciences, Department of Cardiopulmonary Physiotherapy and Rehabilitation, Gazi University, Emek, Ankara, 06490, Turkey. betulyoleri@gazi.edu.tr.ORCID http://orcid.org/0000-0002-0649-7252
Meral Boşnak GüçlüFaculty of Health Sciences, Department of Cardiopulmonary Physiotherapy and Rehabilitation, Gazi University, Emek, Ankara, 06490, Turkey.ORCID http://orcid.org/0000-0002-3861-9912
Tuğba Şişmanlar EyüboğluFaculty of Medicine, Department of Pediatric Pulmonology, Gazi University, Ankara, Turkey.ORCID http://orcid.org/0000-0001-7284-4999
Ayşe Tana AslanFaculty of Medicine, Department of Pediatric Pulmonology, Gazi University, Ankara, Turkey.ORCID http://orcid.org/0000-0002-5360-8517

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimExercise intolerance, muscle weakness, mitochondrial involvement, and slow phosphocreatine metabolism are common, but extrapulmonary impairments in pediatric patients with cystic fibrosis (CF) have not been adequately studied yet. This study compared pulmonary function, upper extremity exercise capacity, muscle oxygenation, peripheral muscle strength, and balance in patients with CF and healthy controls. MATERIALS AND

methodsThirty-one pediatric patients with cystic fibrosis and 30 healthy controls were compared. Pulmonary function was assessed by spirometry; upper extremity functional exercise capacity was evaluated using the 6-minute Pegboard and Ring Test (6PBRT); deltoid muscle oxygenation was measured at rest, during the 6PBRT, and during recovery using near-infrared spectroscopy; shoulder abductor and knee extensor isometric muscle strength were assessed using a hand-held dynamometer; and static and dynamic balance were evaluated using the Biodex Biosway® Portable Balance System and the Y-Balance Test, respectively.

resultsAge and gender were similar in groups (p > 0.05). FEV1%, FVC%, PEF%, FEF25 − 75%, and muscle strength statistically significantly (p < 0.05) decreased in patients. Six-minute PBRT score, deltoid muscle oxygen saturation, and hemoglobin level were similar in groups (p > 0.05). The medial-lateral stability index of patients on soft ground with eyes open was statistically significantly higher than healthy controls (p < 0.05).

conclusionUpper extremity exercise capacity, muscle oxygenation, and most parameters of balance are preserved, and peripheral muscles are weakened in mildly impaired patients with CF. Impaired pulmonary function may impair upper extremity exercise capacity and muscle oxygen metabolism in severe patients with CF, should be investigated.

Indexed as

Cystic FibrosisExerciseMuscle, SkeletalOxygenOxygen ConsumptionPostural BalanceUpper ExtremityAdolescentChildCross-Sectional StudiesExercise ToleranceFemaleHumansMaleMuscle StrengthOxygenCystic fibrosisExercise toleranceMuscle strengthNear-infrared spectroscopyPostural balance

Identifiers

PMID41793435
PMCPMC13287267

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.