Literature DB >> 23681502

Benefits of combining inspiratory muscle with 'whole muscle' training in children with cystic fibrosis: a randomised controlled trial.

Elena Santana-Sosa1, Laura Gonzalez-Saiz1, Iris F Groeneveld2, José R Villa-Asensi3, María I Barrio Gómez de Aguero3, Steven J Fleck4, Luis M López-Mojares1, Margarita Pérez1, Alejandro Lucia5.   

Abstract

BACKGROUND: The purpose of this study (randomised controlled trial) was to assess the effects of an 8-week combined 'whole muscle' (resistance+aerobic) and inspiratory muscle training (IMT) on lung volume, inspiratory muscle strength (PImax) and cardiorespiratory fitness (VO2 peak) (primary outcomes), and dynamic muscle strength, body composition and quality of life in paediatric outpatients with CF (cystic fibrosis, secondary outcomes). We also determined the effects of a detraining period.
METHODS: Participants were randomly allocated with a block on gender to a control (standard therapy) or intervention group (initial n=10 (6 boys) in each group; age 10±1 and 11±1 years). The latter group performed a combined programme (IMT (2 sessions/day) and aerobic+strength exercises (3 days/week, in-hospital)) that was followed by a 4-week detraining period. All participants were evaluated at baseline, post-training and detraining.
RESULTS: Adherence to the training programme averaged 97.5%±1.7%. There was a significant interaction (group×time) effect for PImax, VO2peak and five-repetition maximum strength (leg-press, bench-press, seated-row) (all (p<0.001), and also for %fat (p<0.023) and %fat-free mass (p=0.001), with training exerting a significant beneficial effect only in the intervention group, which was maintained after detraining for PImax and leg-press.
CONCLUSION: The relatively short-term (8-week) training programme used here induced significant benefits in important health phenotypes of paediatric patients with CF. IMT is an easily applicable intervention that could be included, together with supervised exercise training in the standard care of these patients. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  Aerobic fitness/Vo2 Max; Children; Children and exercise; Children's health and exercise

Mesh:

Year:  2013        PMID: 23681502     DOI: 10.1136/bjsports-2012-091892

Source DB:  PubMed          Journal:  Br J Sports Med        ISSN: 0306-3674            Impact factor:   13.800


  18 in total

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Review 5.  Physical function and quality of life in patients with chronic GvHD: a summary of preclinical and clinical studies and a call for exercise intervention trials in patients.

Authors:  C Fiuza-Luces; R J Simpson; M Ramírez; A Lucia; N A Berger
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6.  Respiratory muscle training for cystic fibrosis.

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Journal:  Cochrane Database Syst Rev       Date:  2020-12-17

Review 7.  Respiratory muscle training for cystic fibrosis.

Authors:  Nathan Hilton; Arturo Solis-Moya
Journal:  Cochrane Database Syst Rev       Date:  2018-05-24

Review 8.  Physical exercise training for cystic fibrosis.

Authors:  Thomas Radtke; Sarah J Nevitt; Helge Hebestreit; Susi Kriemler
Journal:  Cochrane Database Syst Rev       Date:  2017-11-01

9.  Effects of home-based respiratory muscle training in children and adolescents with chronic lung disease.

Authors:  Iván Rodríguez Núñez; Daniel Zenteno Araos; Carlos Manterola Delgado
Journal:  J Bras Pneumol       Date:  2014 Nov-Dec       Impact factor: 2.624

10.  Safety and feasibility of a home-based six week resistance training program in juvenile idiopathic arthritis.

Authors:  Cameron Van Oort; Susan M Tupper; Alan M Rosenberg; Jonathan P Farthing; Adam D Baxter-Jones
Journal:  Pediatr Rheumatol Online J       Date:  2013-12-20       Impact factor: 3.054

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