Cystic Fibrosis Clinical Trial
— FIQMODEOfficial title:
Effects of a Strength Exercise Program on Muscular Health in People With CF Treated With Modulators of the Cystic Fibrosis Transmembrane Conductance Regulator Receptor (CFTR)
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.
Status | Recruiting |
Enrollment | 48 |
Est. completion date | December 23, 2025 |
Est. primary completion date | December 23, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 6 Years to 20 Years |
Eligibility | Inclusion Criteria: - patients diagnosed with CF. - patients between 6-20 years of age. - patients receiving treatment with new CFTR protein modulating medication - reading, acceptance and signing of the informed consent form. Exclusion Criteria: - CF patients with symptoms of pulmonary exacerbation during the last four weeks. - with a diagnosis of other cardiorespiratory lung diseases progressing to a symptom of persistent respiratory dysfunction. - CF patients with musculoskeletal alterations that influence assessments. - CF patient who is pregnant during the time of the study - CF patient with cognitive impairment; - CF patient with incomplete dosing of modulator therapy; |
Country | Name | City | State |
---|---|---|---|
Spain | Facultad de Ciencias de la Actividad Física y Deporte - INEF UPM | Madrid |
Lead Sponsor | Collaborator |
---|---|
Universidad Politecnica de Madrid | Carlos III Health Institute, Hospital Infantil Universitario Niño Jesús, Madrid, Spain, Hospital Universitario La Paz, Hospital Universitario Ramon y Cajal, Universidad Europea de Madrid |
Spain,
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* Note: There are 54 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in peripheral muscle strength | Upper and lower limbs muscle strength (kg) will be evaluated using dynamometers. | Baseline, pre-intervention and immediately after the intervention. | |
Primary | 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. | Baseline, pre-intervention and immediately after the intervention | |
Primary | Changes in functional capacity: lower limbs power capacity | 30 seconds sit-to-stand test. Unit of measurement: number of repetitions. | Baseline, pre-intervention and immediately after the intervention | |
Primary | Changes in functional capacity: walking capacity | 10m Time (s) Up and Go tests. | Baseline, pre-intervention and immediately after the intervention | |
Primary | 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. | Baseline, pre-intervention and immediately after the intervention | |
Primary | 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). | Baseline, pre-intervention and immediately after the intervention | |
Secondary | Changes in Pulmonary Function: forced vital capacity (FVC) | Spirometry will assess: forced vital capacity (FVC) in milliliters and percentage of predicted value | Baseline, pre-intervention and immediately after the intervention | |
Secondary | 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. | Baseline, pre-intervention and immediately after the intervention | |
Secondary | Changes in the anthropometric and body composition: Weight | Weight (kg) | Baseline, pre-intervention and immediately after the intervention | |
Secondary | Changes in the anthropometric and body composition: Height | Height (cm) | Baseline, pre-intervention and immediately after the intervention | |
Secondary | Changes in the anthropometric and body composition: BMI | BMI (kg/m2) | Baseline, pre-intervention and immediately after the intervention | |
Secondary | Changes in body composition: Total fat mass | Total fat mass (kg) | Baseline, pre-intervention and immediately after the intervention | |
Secondary | Changes in body composition: FMI | fat mass index (FMI) (kg/m2), | Baseline, pre-intervention and immediately after the intervention | |
Secondary | Changes in body composition: lean mass kg | Lean mass in kg | Baseline, pre-intervention and immediately after the intervention | |
Secondary | Changes in body composition: lean mass % | Lean mass in % | Baseline, pre-intervention and immediately after the intervention | |
Secondary | 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. | Baseline, pre-intervention and immediately after the intervention | |
Secondary | Changes in plasma levels muscle damage biomarkers | Blood levels biomarkers of muscle damage as CK measured in micrograms per litre (mcg/L) | Baseline, pre-intervention and immediately after the intervention | |
Secondary | Changes in plasma levels of inflammation: hs-CRP | High-sensitivity C-reactive protein (hs-CRP) assay in milligrams/litre | Baseline, pre-intervention and immediately after the intervention | |
Secondary | Changes in plasma levels of inflammation: Interleukins | Analysis of interleukins such as IL6, IL-10 in picograms/millilitre | Baseline, pre-intervention and immediately after the intervention |
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