- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01521247
Implementation of a Pediatric-to-adult Asthma Transition Program
Despite the clear and often stated need, a formal transition program does not exist for asthma patients as they move from pediatric to adult care in Western Canada. This population is not having their health care needs met. The investigators proposed study would evaluate a well structured transition program designed to facilitate continuity of care for this at risk patient population.
Primary hypothesis: A pediatric-to-adult asthma transition program will improve the asthma-specific quality of life of young asthma patients in the Calgary area over a 1 year period.
Secondary hypothesis: A pediatric-to-adult asthma transition program will improve asthma control, decrease asthma exacerbations, and reduce health care utilization in young asthma patients in the Calgary area over a 1 year period.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
Alberta
-
Calgary, Alberta, Canada, T3B 6A8
- Calgary Regional Pediatric Asthma Clinic
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- clinical diagnosis of asthma (as confirmed by a pediatric respirologist or pediatrician with asthma expertise, and including evidence of variable airflow obstruction, bronchial hyperresponsiveness, airway inflammation, and/or response to therapy)
Exclusion Criteria:
- patients who are known to be non-adherent within the Calgary Regional Pediatric Asthma Clinic (defined as >50% missed appointments over a 2 year period)
- patients unable to complete pulmonary function testing
- patients with a history of significant respiratory comorbid conditions (including history of cystic fibrosis, alpha-1 antitrypsin deficiency, and lung transplant - rhinosinusitis patients will not be excluded)
- patients unable to provide consent.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Ingen indgriben: Kontrolgruppe
Sædvanlig pleje.
|
|
Andet: Asthma Transition Program
|
Asthma Education.
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Asthma Quality of Life Questionnaire with Standardized Activities [AQLQ(S)]
Tidsramme: 12 months
|
AQLQ(S) will be recorded at baseline, 6 months, and 12 months.
The primary outcome will be the change in AQLQ(S) from baseline to 12 months.
|
12 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Asthma Control Questionnaire (ACQ)
Tidsramme: 12 months
|
The ACQ will be administered at baseline, 6 months, and 12 months.
The secondary outcome will assess change in ACQ from baseline to 12 months.
|
12 months
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Studieleder: Mary Noseworthy, MD, Alberta Children's Hospital
- Studieleder: Rodel Padua, RRT
- Studieleder: Sheldon Spier, MD, Alberta Children's Hospital
- Studieleder: Ward Flemons, MD, University of Calgary
- Ledende efterforsker: Warren Davidson, MD, University of Calgary
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- AJMG-2010
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