- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01964469
Consumer Access to Personal Health Information for Asthma Self-Management (ASMA)
15. august 2019 opdateret af: Chris Licskai, Lawson Health Research Institute
Consumer Access to Personal Health Information for Asthma Self-Management Phase 2 (Pilot Implementation)
This study is to compare Smart phone mobile device and/or web based application asthma action plan to the standard of care paper based asthma action plan within an asthma program.
The Primary hypothesis: Health Outcome - The Breathe mobile health and web-based application improves asthma related quality of life more than conventional best practice
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This study is a multi-centre, randomized controlled trial comparing a web-based (Smart phone mobile device, tablet and/or personal computer PC) asthma action plan application to best practice/usual care within an asthma program.
A third external comparator arm will compare participants to all patients with asthma in Ontario using data obtained from the Ontario Asthma Surveillance Information System (OASIS) cohort, created from administrative data sets within the Institute for Clinical Evaluative Sciences (ICES).
Subjects will be randomly assigned in blocks of four, stratified by site to, in a ratio of 1:1 intervention or control arms.
The study will enrol approximately 400 patients in total at all study sites.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
344
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Ontario
-
Amherstburg, Ontario, Canada
- Amherstburg FHT
-
Chatham, Ontario, Canada
- Chatham-Kent FHT
-
Harrow, Ontario, Canada
- Harrow FHT
-
Kingston, Ontario, Canada
- Kingston Hospital Asthma Clinic
-
Leamington, Ontario, Canada, N8H 1N8
- Leamington FHT
-
London, Ontario, Canada
- St. Joseph's Hospital Asthma Clinic
-
Sault Ste. Marie, Ontario, Canada
- Sault St. Marie Group Health Centre
-
Windsor, Ontario, Canada
- Windsor FHT
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Diagnosis of asthma
- Age 18 of age or older
- Familiar with web technology
- Provide consent
- Understand/read/write English
Exclusion Criteria:
- Indication of other chronic lung diseases in the opinion of the physician that would impact their ability to participate in the trial or affect quality of life (Cystic Fibrosis, Chronic Obstructive Pulmonary Disease, Bronchiectasis)
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Placebo komparator: Written self-management action plan
Usual Care: Evidence-based best practice within the primary care asthma program including written self-management action plan and regular clinical review.
|
Evidence-based best practice primary care asthma program including asthma self-management education replacing the written self-management action plan with the Breathe mobile health and web-based application
|
|
Eksperimentel: mobile & web based action plan
Evidence-based best practice within the primary care asthma program, replacing the written action plan with the Breathe mobile health and web-based application.
|
Evidence-based best practice primary care asthma program including asthma self-management education replacing the written self-management action plan with the Breathe mobile health and web-based application
|
|
Ingen indgriben: Administrative data set
Health services use will be evaluated comparatively against our intervention population and our control and we will include health services utilization data from one year prior randomization.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Health Outcome - Quality of Life
Tidsramme: 6 months
|
Health Outcome - The Breathe mobile health and web-based application improves asthma related quality of life more than conventional best practice.
|
6 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Quality - Health Care Utilization
Tidsramme: 1 year
|
Appropriateness of Care - Individuals with asthma who use the intervention will experience a decrease in the number of unplanned health system encounters
|
1 year
|
Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Health Outcome - Quality
Tidsramme: 1 year
|
Improvements in symptom profile greater than conventional best practice.
|
1 year
|
|
Health Outcome - Quality of Life
Tidsramme: 6 months
|
Per protocol evaluation of the primary outcome, quality of life.
It is anticipated that some subjects randomized to the intervention arm will not use the smartphone application.
We seek to evaluate the primary outcome in those subjects who were adherent to the application compared to control subjects.
|
6 months
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Christopher Licskai, Lawson Health Research Institution
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. februar 2013
Primær færdiggørelse (Faktiske)
1. juni 2014
Studieafslutning (Faktiske)
1. marts 2016
Datoer for studieregistrering
Først indsendt
21. januar 2013
Først indsendt, der opfyldte QC-kriterier
14. oktober 2013
Først opslået (Skøn)
17. oktober 2013
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
19. august 2019
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
15. august 2019
Sidst verificeret
1. august 2019
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 00000940
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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