Literature DB >> 33577586

Measurement properties of the one-minute sit-to-stand test in children and adolescents with cystic fibrosis: A multicenter randomized cross-over trial.

Yann Combret1,2,3, Fairuz Boujibar4, Charlotte Gennari5, Clément Medrinal3,6,7, Sophie Sicinski8, Tristan Bonnevie9,10, Francis-Edouard Gravier9,10, Muriel Laurans5, Christophe Marguet8,11, Pascal Le Roux1, Bouchra Lamia3,10,12, Guillaume Prieur2,3,10, Grégory Reychler2,13.   

Abstract

BACKGROUND: Functional exercise capacity assessment is recommended in children with cystic fibrosis (CF). The six-minute walk test (6MWT) is a valid evaluation of exercise capacity but can be technically complex. Inversely, the sit-to-stand test (STST) is a simple method to evaluate exercise capacity, and is validated in healthy children and adults with CF. This study aimed to evaluate STST measurement properties in children and adolescents with CF.
METHODS: In this multicenter study, children with CF (6 to 18 years) performed two iterations of both the STST and the 6MWT in a randomized order. Criterion validity was determined by assessing correlations between STST repetitions and 6MWT distance (6MWD). Intra-rater reliability, test-retest repeatability, mean bias and limits of agreement were also assessed. Relationships with other outcomes (i.e. respiratory and quadriceps muscle strength) and cardio-respiratory responses were analysed for both tests.
RESULTS: Thirty-six children with CF were included (mean age 12.0 ±3.5 years and FEV1 95.8 ±25.0%). On average, 39.6 ±10.5 repetitions were performed during the STST and mean 6MWD was 596.0 ±102.6 meters. STST number of repetitions was significantly correlated with 6MWD (r = 0.48; p<0.01). Both tests had very good intra-rater reliability (ICCSTST = 0.91 (95%CI 0.76-0.96) and ICC6MWT = 0.94 (95%CI 0.85-0.97)), and a significant test-retest learning effect. The number of STST repetitions was not correlated with quadriceps or respiratory muscle strength test, and the STST induced fewer cardio-respiratory responses than the 6MWT.
CONCLUSIONS: The STST is an easy-to-use functional test with moderate criterion validity when compared to the 6MWT in children with CF, probably because both tests measure different components of functional exercise capacity. The STST is useful when the 6MWT is unfeasible, however further investigations are required to explore the clinical implications of STST results in children with CF. CLINICAL TRIAL REGISTRATION: NCT03069625.

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Year:  2021        PMID: 33577586      PMCID: PMC7880481          DOI: 10.1371/journal.pone.0246781

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


  37 in total

1.  Comparison of the Sit-to-Stand Test with 6 min walk test in patients with chronic obstructive pulmonary disease.

Authors:  S Ozalevli; A Ozden; O Itil; A Akkoclu
Journal:  Respir Med       Date:  2006-06-27       Impact factor: 3.415

2.  Fixed Handheld Dynamometry Provides Reliable and Valid Values for Quadriceps Isometric Strength in People With Chronic Obstructive Pulmonary Disease: A Multicenter Study.

Authors:  Kim-Ly Bui; Sunita Mathur; Gail Dechman; François Maltais; Pat Camp; Didier Saey
Journal:  Phys Ther       Date:  2019-09-01

3.  Correlation between posture, balance control, and peripheral muscle function in adults with cystic fibrosis.

Authors:  Tatiana Rafaela Lemos Lima; Fernando Silva Guimarães; Arthur Sá Ferreira; Jennifer Taborda Silva Penafortes; Vívian Pinto Almeida; Agnaldo José Lopes
Journal:  Physiother Theory Pract       Date:  2013-07-26       Impact factor: 2.279

4.  Expiratory muscle strength and functional exercise tolerance in adults with cystic fibrosis: a cross-sectional study.

Authors:  Simone Gambazza; Valentina Turrin; Chiara Speziali; Anna Brivio; Lauretta Valmarana; Federica Carta; Anna Marta Clotilde Bulfamante; Carla Colombo
Journal:  Physiother Res Int       Date:  2018-06-26

5.  The six-minute walking test in children with cystic fibrosis: reliability and validity.

Authors:  V A Gulmans; N H van Veldhoven; K de Meer; P J Helders
Journal:  Pediatr Pulmonol       Date:  1996-08

6.  Cardiopulmonary Exercise Testing Provides Additional Prognostic Information in Cystic Fibrosis.

Authors:  Helge Hebestreit; Erik H J Hulzebos; Jane E Schneiderman; Chantal Karila; Steven R Boas; Susi Kriemler; Tiffany Dwyer; Margareta Sahlberg; Don S Urquhart; Larry C Lands; Felix Ratjen; Tim Takken; Liobou Varanistkaya; Viktoria Rücker; Alexandra Hebestreit; Jakob Usemann; Thomas Radtke
Journal:  Am J Respir Crit Care Med       Date:  2019-04-15       Impact factor: 21.405

7.  Six-minute walk test in children and adolescents with cystic fibrosis.

Authors:  Maristela Trevisan Cunha; Tatiana Rozov; Rosangela Caitano de Oliveira; José R Jardim
Journal:  Pediatr Pulmonol       Date:  2006-07

8.  The 1-min sit-to-stand test--A simple functional capacity test in cystic fibrosis?

Authors:  Thomas Radtke; Milo A Puhan; Helge Hebestreit; Susi Kriemler
Journal:  J Cyst Fibros       Date:  2015-09-09       Impact factor: 5.482

Review 9.  Six-minute walk test as a determinant of the functional capacity of children and adolescents with cystic fibrosis: A systematic review.

Authors:  Cibelle Andrade Lima; Armèle Dornelas de Andrade; Shirley Lima Campos; Daniella Cunha Brandão; Ianny Pereira Mourato; Murilo Carlos Amorim de Britto
Journal:  Respir Med       Date:  2018-02-26       Impact factor: 3.415

10.  Population-based reference values for the 1-min sit-to-stand test.

Authors:  Alexandra Strassmann; Claudia Steurer-Stey; Kaba Dalla Lana; Marco Zoller; Alexander J Turk; Paolo Suter; Milo A Puhan
Journal:  Int J Public Health       Date:  2013-08-24       Impact factor: 3.380

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  2 in total

Review 1.  Physical activity and exercise training in cystic fibrosis.

Authors:  Thomas Radtke; Sherie Smith; Sarah J Nevitt; Helge Hebestreit; Susi Kriemler
Journal:  Cochrane Database Syst Rev       Date:  2022-08-09

2.  Psychometric properties of the sit-to-stand test for patients with pulmonary hypertension: A systematic review protocol.

Authors:  Natália Lopes Cardoso; Joceline Ferezini de Sá; Larissa F E do Nascimento; Luciana A Mendes; Selma Bruno; Rodrigo Torres-Castro; Guilherme A F Fregonezi; Vanessa R Resqueti
Journal:  PLoS One       Date:  2022-10-05       Impact factor: 3.752

  2 in total

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