Respiratory Function in Patients With Post-tuberculosis Lung Impairment
NCT ID: NCT03821285
Last Updated: 2019-01-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
100 participants
INTERVENTIONAL
2019-02-14
2021-01-14
Brief Summary
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Detailed Description
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1. After signature of the informed consent to the study, patients will undergo a Pre-screening Visit: data on medical history, current pharmacological therapies, smoking (pack/year), vaccinations, physical examination, vital parameters (blood pressure, heart rate, respiratory rate, oxygen saturation in arterial blood), co-morbidities and Mini Mental State Examination will be collected.
2. Screening Visit (before the RP), during the visit the following data will be collected: number of TB disease episodes, detailed data on the last TB episode (age at onset of TB symptoms, age at TB diagnosis, anti-TB treatment duration, anti-TB drugs administered, socio-economic conditions, education level, physical examination, vital parameters, oxygen saturation in arterial blood, heart rate and respiratory rate). Pulmonary rehabilitation program tailored according to specific patient's needs.
3. Baseline assessment of respiratory function: arterial blood gas (ABG) analysis, spirometry, diffusing capacity of the lungs for carbon monoxide (DLCO), overnight oximetry, electrocardiogram (ECG), chest X-ray (CXR), High-resolution computed tomography (HRCT)
4. Assessment of the rehabilitation programme: functional evaluation (6MWT), muscle strength evaluation (five-repetition sit-to-stand test (5STS)), respiratory muscle strength (maximum inspiratory pressure (MIP) and maximum expiratory pressure (MEP)), symptoms evaluation (Dyspnea: Medical Research Council Questionnaire (MRC), Modified Borg pre/post 6MWT, Baseline and Transition Dyspnea Indexes (BDI-TDI) and Fatigue: Modified Borg pre/post 6MWT)
5. Assessment of the Quality of Life (QoL): CAT and St George's Respiratory Questionnaire.
Final assessment:
A final assessment will be done at the end of the rehabilitation programme and will include:
c) Only ABG, spirometry and DLCO d) and e).
Pulmonary rehabilitation programme
PR programme will include:
At least 15 aerobic-training sessions by cycle ergometer supervised by a respiratory therapist (5 session per week, 30 minutes each: 5 minutes warm up, 20 minutes training and 5 minutes warm-down) at constant load (calculated with Hill equation, Hill K, et al. Estimating maximum work rate during incremental cycle ergometry testing from six-minute walk distance in patients with chronic obstructive pulmonary disease. Arch Phys Med Rehabil. 2008;89(9):1782-7.) with an adherence of at least 80%.
1. At least 15 strength-training sessions for peripheral muscles (30 minutes calisthenics exercise) with an adherence of at least 80%.
2. At least 3 face to face and/or group educational sessions, for:
* Optimization of inhalation techniques
* Exercise training and maintenance programs
* Daily physical activity
* Airways clearance techniques
* Long oxygen therapy home management.
3. According to individual needs, the PR program should include:
* airways clearance techniques
* inspiratory muscles training (with Threshold®)
Monitoring Anonymous data will be collected in a common electronic format (excel database).
Adverse events (AEs) and severe adverse events (SAEs) will be reported and registered.
Follow-up
Follow-up visit 1 year after completion of RP will include:
c) Only ABG, spirometry, DLCO and overnight oximetry d) and e) Statistical analysis A two-tailed p-value less than 0.05 will be considered statistically significant.
Qualitative and quantitative variables will be described with absolute and relative (percentages) frequencies and means (standard deviations -SD) or medians (interquartile ranges -IQR) depending on their normality, respectively. The mean difference between the two study groups in the 6MWT will be evaluated using the Student's t-test. Differences in the variables associated to the secondary objectives will be evaluated using the Chi-square or Student's t-test for qualitative and quantitative variables. A two-tailed p-value less than 0.05 will be considered statistically significant.
Conditions
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Study Design
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NA
SINGLE_GROUP
SCREENING
NONE
Study Groups
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pulmonary rehabilitation
Pulmonary rehabilitation program
Pulmonary Rehabilitation
Pulmonary rehabilitation programme:15 aerobic-training sessions, 15 strength-training sessions for peripheral muscles, 3 face to face and/or Group educational sessions, if needed airways clearance techniques and/or inspiratory muscles training
Interventions
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Pulmonary Rehabilitation
Pulmonary rehabilitation programme:15 aerobic-training sessions, 15 strength-training sessions for peripheral muscles, 3 face to face and/or Group educational sessions, if needed airways clearance techniques and/or inspiratory muscles training
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Musculoskeletal disorders contraindicating participation in the PR program
* Cognitive impairment (Mini Mental State Examination \<22)
* Unable to sign informed consent
ALL
No
Sponsors
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Fondazione Salvatore Maugeri
OTHER
Azienda Ospedaliero Universitaria di Sassari
OTHER
Instituto Nacional de Enfermedades Respiratorias
OTHER_GOV
UniversitĂ degli Studi dell'Insubria
OTHER
Responsible Party
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Dina Visca
Principal Investigator
Principal Investigators
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Giovan Battista Migliori, Prof
Role: STUDY_DIRECTOR
ICS Maugeri, IRCCS
Locations
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ICS Maugeri, IRCCS
Tradate, Varese, Italy
Countries
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Central Contacts
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Facility Contacts
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References
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Tiberi S, Munoz-Torrico M, Duarte R, Dalcolmo M, D'Ambrosio L, Migliori GB. New drugs and perspectives for new anti-tuberculosis regimens. Pulmonology. 2018 Mar-Apr;24(2):86-98. doi: 10.1016/j.rppnen.2017.10.009. Epub 2018 Feb 24.
Munoz-Torrico M, Rendon A, Centis R, D'Ambrosio L, Fuentes Z, Torres-Duque C, Mello F, Dalcolmo M, Perez-Padilla R, Spanevello A, Migliori GB. Is there a rationale for pulmonary rehabilitation following successful chemotherapy for tuberculosis? J Bras Pneumol. 2016 Sep-Oct;42(5):374-385. doi: 10.1590/S1806-37562016000000226.
Other Identifiers
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2215CE
Identifier Type: -
Identifier Source: org_study_id
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