Literature DB >> 11836799

Randomized controlled study of in-hospital exercise training programs in children with cystic fibrosis.

H C Selvadurai1, C J Blimkie, N Meyers, C M Mellis, P J Cooper, P P Van Asperen.   

Abstract

The aim of this study was to compare aerobic and resistance training in children with cystic fibrosis (CF) admitted to hospital with an intercurrent pulmonary infection with a control group. The subjects were randomized into three groups on the first day of admission. The fat-free mass (FFM) was calculated, using the skin fold thickness from four sites (biceps, triceps, subscapular, and iliac crest). Pulmonary function tests were performed within 36 hr of admission and repeated on discharge from the hospital, and again at 1 month after discharge. All subjects performed an incremental treadmill exercise test, using a modified Bruce protocol. Lower limb strength was measured using a Cybex dynamometer. An assessment of quality of life was made using the Quality of Well Being Scale, as previously reported. Activity levels were measured using a 7-day activity diary, and subjects also wore an accelerometer on their hips. There were no significant differences between the three groups in terms of disease severity, and length of stay in hospital. Subjects in all three groups received intravenous antibiotics and nutritional supplementation as determined by the physician. Children randomized to the aerobic training group participated in aerobic activities for five sessions, each of 30-min duration, a week. The children randomized to the resistance training group exercised both upper and lower limbs against a graded resistance machine. Subjects in the control group received standard chest physiotherapy. Our study demonstrated that children who received aerobic training had significantly better peak aerobic capacity, activity levels, and quality of life than children who received the resistance training program. Children who received resistance training had better weight gain (total mass, as well as fat-free mass), lung function, and leg strength than children who received aerobic training. A combination of aerobic and resistance training may be the best training program, and future studies to assess optimal training programs for CF patients are indicated. Copyright 2002 Wiley-Liss, Inc.

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Mesh:

Year:  2002        PMID: 11836799     DOI: 10.1002/ppul.10015

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  55 in total

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3.  Validation of activity questionnaires in patients with cystic fibrosis by accelerometry and cycle ergometry.

Authors:  Katharina C Ruf; Sonja Fehn; Michèle Bachmann; Alexander Moeller; Kristina Roth; Susi Kriemler; Helge Hebestreit
Journal:  BMC Med Res Methodol       Date:  2012-04-03       Impact factor: 4.615

4.  Relationship between breath-hold time and physical performance in patients with cystic fibrosis.

Authors:  Maria Barnai; Istvan Laki; Kalman Gyurkovits; Lajos Angyan; Gyöngyi Horvath
Journal:  Eur J Appl Physiol       Date:  2005-07-09       Impact factor: 3.078

5.  Exercise intensity self-regulation using the OMNI scale in children with cystic fibrosis.

Authors:  Linda W Higgins; Robert J Robertson; Sheryl F Kelsey; Marian B Olson; Leslie A Hoffman; Paul J Rebovich; Luke Haile; David M Orenstein
Journal:  Pediatr Pulmonol       Date:  2012-09-19

6.  Physical activity recommendations for children with specific chronic health conditions: Juvenile idiopathic arthritis, hemophilia, asthma and cystic fibrosis.

Authors:  J Philpott; K Houghton; A Luke
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7.  The evidence regarding exercise training in the management of cystic fibrosis: a systematic review.

Authors:  Michael J Shoemaker; Heather Hurt; Leah Arndt
Journal:  Cardiopulm Phys Ther J       Date:  2008-09

8.  Exercise training in children and adolescents with cystic fibrosis: theory into practice.

Authors:  Craig A Williams; Christian Benden; Daniel Stevens; Thomas Radtke
Journal:  Int J Pediatr       Date:  2010-09-19

Review 9.  Patient-reported outcomes in cystic fibrosis.

Authors:  Christopher H Goss; Alexandra L Quittner
Journal:  Proc Am Thorac Soc       Date:  2007-08-01

10.  Short-Term Effect of Different Physical Exercises and Physiotherapy Combinations on Sputum Expectoration, Oxygen Saturation, and Lung Function in Young Patients with Cystic Fibrosis.

Authors:  Susi Kriemler; Thomas Radtke; Gregor Christen; Marta Kerstan-Huber; Helge Hebestreit
Journal:  Lung       Date:  2016-05-04       Impact factor: 2.584

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