- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03804632
Assessment of Asthma Control Level in Primary Care Setting in Malaysia (ASCOPE)
A Prospective Observational Multi Center Study to Assess the Level of Asthma Control at Government Health Clinics (Klinik Kesihatan) in Malaysia.
Studieoversigt
Status
Betingelser
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Faktiske)
Kontakter og lokationer
Studiesteder
-
-
Negeri Sembilan
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Port Dickson, Negeri Sembilan, Malaysia
- Research Site
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Seremban, Negeri Sembilan, Malaysia
- Research Site
-
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Penang
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George Town, Penang, Malaysia
- Research Site
-
-
Perak
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Pantai Remis, Perak, Malaysia
- Research Site
-
-
Sabah
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Kota Kinabalu, Sabah, Malaysia
- Research Site
-
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Sarawak
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Asajaya, Sarawak, Malaysia
- Research Site
-
-
Selangor
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Banting, Selangor, Malaysia
- Research Site
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Rawang, Selangor, Malaysia
- Research Site
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Terengganu
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Bandar Permaisuri, Terengganu, Malaysia
- Research Site
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Kuala Terengganu, Terengganu, Malaysia
- Research Site
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-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- Malaysians who have been diagnosed with Asthma by a physician verified by an investigator and seen at government health clinic (Klinik Kesihatan) from October - December 2017
- Be at least 18 years of age
Exclusion Criteria:
- Clinical features suggesting emphysema or chronic bronchitis and other chronic lung diagnosis
- Pregnancy
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
|---|
|
GINA-defined clinical diagnosis of Asthma
All patients with GINA-defined clinical diagnosis of Asthma seen at respiratory clinic from October to December 2017 with age 18 and above
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Level of GINA-defined asthma control
Tidsramme: up to 8 months
|
GINA-defined asthma control: According to clinical characteristics that include daytime symptoms, limitations of activity, nocturnal symptoms/awakening, need for reliever/rescue treatment.
Patient's are classified as controlled, partially controlled or uncontrolled.
|
up to 8 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Typer af medicin ordineret til astmakontrol
Tidsramme: op til 8 måneder
|
Farmakologisk behandling brugt til astmakontrol
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op til 8 måneder
|
|
Asthma control level
Tidsramme: up to 8 months
|
Asthma control is evaluated by patients' self-completion of the Asthma Control Test (ACT).
The ACT is a reliable, valid tool that helps physicians identify patients with uncontrolled asthma in a clinical setting.
The questionnaire assesses the frequency of asthma symptoms and patients' own perception of asthma control during the previous 4 weeks.
Based on the sum of scores, complete asthma control (25 points), well-controlled asthma (20-24 points) or no asthma control (≤19 points) is revealed.
|
up to 8 months
|
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Adherence level in patients with inhalers
Tidsramme: up to 8 months
|
Adherence level measured by Malaysia Medication Adherence Scale (MALMAS) The first item of the MALMAS has five responses: (1) All the time, (2) Often, (3) Sometimes, (4) Rarely and (5) Never. The remaining seven items have a dichotomous response of "Yes" or "No". The responses in the MALMAS were scored based on the MMAS-8 where the total score ranged from 0 to 8. Both instruments categorized medication adherence based on the total scores obtained: low adherence (total score<6), medium adherence (6 to < 8) and high adherence (total score = 8) |
up to 8 months
|
Samarbejdspartnere og efterforskere
Sponsor
Publikationer og nyttige links
Hjælpsomme links
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
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- D2287R00120
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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