- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03227341
Pulmonary Rehabilitation in Asthma Control
Does Pulmonary Rehabilitation Contribute to Asthma Control?
Studieoversigt
Detaljeret beskrivelse
Asthma treatment is not only medical, it also requires a comprehensive care including nonpharmacological treatment. Pulmonary rehabilitation represents the most important part of the comprehensive care. The investigators aimed to evaluate the efficacy of pulmonary rehabilitation in patients with uncontrolled and partially controlled asthma.
Asthma patients referred to pulmonary rehabilitation (PR) unit were classified according to asthma control test; as partially controlled patients (Group 1), and as uncontrolled patients (Group 2). All patients received of a 8 week pulmonary rehabilitation program. Asthma control tests, pulmonary function tests, arterial blood gases analysis, dyspnea perception, quality of life, exercise capacity, anxiety and depression assessments were performed before and after pulmonary rehabilitation.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Asthmatic patients referred from the outpatient clinic to Pulmonary Rehabilitation unit was confirmed according to GINA guidelines
Exclusion Criteria:
- If the initial diagnosis cannot be confirmed, the patient excluded from the study
- Patients were under medical treatment of -6 months and considered clinically stable.
- Patients with cardiovascular, other lung diseases (pneumoconiosis, pulmonary tuberculosis, interstitial lung disease), or musculoskeletal diseases that would impair exercise training were excluded from the study.
- Also subjects with lack of motivation, poor compliance (not attending the program more than 2 times) or having transport problems were excluded from the study
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Andet: patients with uncontrolled asthma.
8 week pulmonary rehabilitation program
|
8 week exercise program including breathing exercises consisted of pursed-lip breathing, diaphragmatic breathing and thoracic expansion exercises, relaxation and stretching exercises, upper and lower extremity muscle strength training, and aerobic exercises.
In addition, bronchial hygiene techniques and dyspnea-reducing positions
|
Andet: patients with partially controlled asthma
8 week pulmonary rehabilitation program
|
8 week exercise program including breathing exercises consisted of pursed-lip breathing, diaphragmatic breathing and thoracic expansion exercises, relaxation and stretching exercises, upper and lower extremity muscle strength training, and aerobic exercises.
In addition, bronchial hygiene techniques and dyspnea-reducing positions
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Asthma control test score
Tidsramme: 4 weeks
|
A test measured the control of asthma
|
4 weeks
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Exercise capacity
Tidsramme: 6 minute
|
Six minute walk test
|
6 minute
|
Dyspnea
Tidsramme: 1 year
|
MMRC Dyspnea Scale
|
1 year
|
Quality of Life
Tidsramme: 1 year
|
St. George Respiratory Questionnaire
|
1 year
|
Pulmonary Function Test
Tidsramme: 1 hour
|
FEV1, FVC, DLCO
|
1 hour
|
Arterial Blood Gas
Tidsramme: 1 hour
|
PaO2, PaCO2, SaO2
|
1 hour
|
Anxiety and Depression
Tidsramme: 1 week
|
Hospital Anxiety and Depression Scale
|
1 week
|
Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- KCU123
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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