Self-Management Using Smartphone Application for Chronic Disease Care in Real siTuation (SMART-Asthma): Adult

NCT ID: NCT01918293

Last Updated: 2013-11-27

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-09-30

Study Completion Date

2013-10-31

Brief Summary

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Bronchial asthma is an chronic airway disease with bronchial hypersensitivity due to inflammation and bronchial muscle contraction. It can cause recurrent dyspnea, cough, wheezing and severe life-threatening attack and lower quality of life. In addition, it make large amount of socioeconomic loss as about 3.7 billion US dollars.

Detailed Description

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Conditions

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BRONCHIAL ASTHMA

Keywords

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ASTHMA SMARTPHONE APPLICATION

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Blinding Strategy

NONE

Study Groups

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SMART arm

Using smartphone application for control of asthma

Group Type EXPERIMENTAL

SMART ARM

Intervention Type DEVICE

The smartphone application for self-management of Asthma offers symptom diary, general information for asthma, the information of asthma drugs,the guideline for inhaler and the specific action plan according to daily symptom and FEV1.

conventional arm

non-using smartphone application for control asthma

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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SMART ARM

The smartphone application for self-management of Asthma offers symptom diary, general information for asthma, the information of asthma drugs,the guideline for inhaler and the specific action plan according to daily symptom and FEV1.

Intervention Type DEVICE

Other Intervention Names

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SMART-Asthma

Eligibility Criteria

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Inclusion Criteria

* using smartphone
* alleged bronchial asthma over 3months \& positive of bronchodilator response test or bronchial provocation test

Exclusion Criteria

* COPD
* active pulmonary TUBERCULOSIS
* Acute exacerbation within 4weeks
* severe psychological disorder
* severe systemic disease; severe LC, ESRD ...
* MALIGNANCY
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Inje University

OTHER

Sponsor Role lead

Responsible Party

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Jongha Park

Study principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Haeundae Paik Hospital

Busan, , South Korea

Site Status

Countries

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South Korea

Other Identifiers

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SMART-ASTHMA (ADULT)

Identifier Type: -

Identifier Source: org_study_id