Recently, the treatment of Cystic Fibrosis (CF) incorporated new modulators/enhancers of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). It is thus increasingly important to study the side effects of these drugs, their extrapulmonary effects and possible interaction with other drugs and with exercise. For this purpose, a randomized controlled trial is proposed to determine the effects of a telematic exercise intervention on muscle health, in a group of 48 children and adolescents with CF treated with these new generation CFTR modulators. They will be randomly assigned to two groups (exercise and control group). The effect of the intervention will be analysed measuring the variables of muscle health, cardiorespiratory fitness, lung function, body composition, inflammatory biomarkers and miRNAs. After completion of the intervention program, adherence to exercise and clinical evolution after one year will be analysed.
Specific objectives 1. To determine the effects of a strength exercise intervention in a group of children and adolescents with cystic fibrosis treated with new generation CFTR modulators on: (1.i) peripheral muscle strength; (1.ii) respiratory muscle strength; (1.iii) muscle mass and (1.iv) biomarkers of muscle damage. 2. To determine the effects of a strength exercise intervention in a group of children and adolescents with cystic fibrosis being treated with new generation CFTR modulators on: (2.i) cardiorespiratory fitness; (2.ii) body composition and (2.iii) lung function. 3. To determine the effects of a strength-based exercise intervention in a group of children and adolescents with cystic fibrosis treated with new-generation CFTR modulators on: (3.i) biomarkers of inflammatory status and (3.ii) expression of associated miRNAs. 4. To determine the effects of a strength-based exercise intervention in a group of children and adolescents with cystic fibrosis treated with the new generation CFTR modulators on the levels of Elexaxcaftor/Ivacaftor/Tezacaftor and their metabolites. 5. To assess the clinical evolution and adherence to exercise after 6 months of the programme in children and adolescents with cystic fibrosis treated with the new generation of CFTR modulators.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
48
16-week exercise intervention: At the beginning of the intervention, we will conduct a face-to-face familiarisation session with the exercises of the training programme. The intervention will consist of 2 sessions/week for 16 weeks. Each session consists of three stages: (i) Warm-up: 10 min of joint mobility and low intensity exercises involving the musculature to be worked in that session; (ii) Main part: circuit training mainly composed of strength exercises targeting the different muscle groups of the body and playing activities (iii) Cool down: 10 min with guided breathing work and stretching of the main muscle groups worked
Facultad de Ciencias de la Actividad Física y Deporte - INEF UPM
Madrid, Madrid, Spain
Changes in peripheral muscle strength
Upper and lower limbs muscle strength (kg) will be evaluated using dynamometers.
Time frame: Baseline, pre-intervention and immediately after the intervention.
Changes in inspiratory/expiratory muscle strength (MIP/MEP) (cmH2O)
Inspiratory and expiratory muscle strength: maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) will be measured.
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in functional capacity: lower limbs power capacity
30 seconds sit-to-stand test. Unit of measurement: number of repetitions.
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in functional capacity: walking capacity
10m Time (s) Up and Go tests.
Time frame: Baseline, pre-intervention and immediately after the intervention
Change in Cardiorespiratory fitness: maximal oxygen consumption
To assess cardiorespiratory fitness, a treadmill and a gas analyser will be used. The test aims to determine maximal oxygen consumption (VO2peak in ml/kg/min). VO2peak will be recorded as the highest value obtained during a continuous 30 s period.
Time frame: Baseline, pre-intervention and immediately after the intervention
Change in Cardiorespiratory fitness: Ventilatory threshold VT1
To assess cardiorespiratory fitness, a treadmill and a gas analyser will be used. The test aims to determine the ventilatory threshold VT1 in response to maximal effort. VT1 will be determined using the criteria of an increase in both ventilatory equivalent for oxygen consumption (VE/VO2) and end-tidal oxygen pressure without an increase in ventilatory equivalent for carbon dioxide production (VE/VCO2).
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in Pulmonary Function: forced vital capacity (FVC)
Spirometry will assess: forced vital capacity (FVC) in milliliters and percentage of predicted value
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in Pulmonary Function: Forced expiratory volume in the first second (FEV1)
Spirometry will assess: forced expiratory volume in the first second (FEV1).Data will be expressed in absolute values and z-score based on the Global Lung Initiative (GLI) reference equation establishing as a limit of normality (LIN) a z-score value for FEV1 between -1.64 and + 1.64.
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in the anthropometric and body composition: Weight
Weight (kg)
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in the anthropometric and body composition: Height
Height (cm)
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in the anthropometric and body composition: BMI
BMI (kg/m2)
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in body composition: Total fat mass
Total fat mass (kg)
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in body composition: FMI
fat mass index (FMI) (kg/m2),
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in body composition: lean mass kg
Lean mass in kg
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Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in body composition: lean mass %
Lean mass in %
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in quality of life using the Cystic Fibrosis Questionnaire
Scores range from 0 to 100 with higher scores corresponding to better quality of life.
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in plasma levels muscle damage biomarkers
Blood levels biomarkers of muscle damage as CK measured in micrograms per litre (mcg/L)
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in plasma levels of inflammation: hs-CRP
High-sensitivity C-reactive protein (hs-CRP) assay in milligrams/litre
Time frame: Baseline, pre-intervention and immediately after the intervention
Changes in plasma levels of inflammation: Interleukins
Analysis of interleukins such as IL6, IL-10 in picograms/millilitre
Time frame: Baseline, pre-intervention and immediately after the intervention