Evaluate Efficacy of Respiratory Rehabilitation Personalized Mobile Services for Respiratory Diseases
NCT ID: NCT03432117
Last Updated: 2018-02-28
Study Results
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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COMPLETED
NA
179 participants
INTERVENTIONAL
2017-05-15
2018-01-06
Brief Summary
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Detailed Description
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Patients in Group A\&B were provided with mobile application and wearable O2 saturation machine and mobile application monitors physical activity and provides
1. how to do stretching, weight training with The-ra Band
2. daily and weekly target of exercise
3. alarm algorithms depending on patient's respiratory status(purse rate and O2 saturation)
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Fixed respiratory rehabilitation program(A)
respiratory rehabilitation program for 12 weeks
Fixed respiratory rehabilitation
There are 6 step-exercise presented in the application and initial target of exercise will be set according to subject condition. After subject completes targeted exercise, next step will be started.
Mixed respiratory rehabilitation program(B)
Fixed respiratory rehabilitation for 6 weeks, and then responsive respiratory rehabilitation for 6 weeks
Fixed respiratory rehabilitation
There are 6 step-exercise presented in the application and initial target of exercise will be set according to subject condition. After subject completes targeted exercise, next step will be started.
Responsive respiratory rehabilitation
The application provide responsive exercise program by changing type and numbers of exercise according to subject condition and exercise ability (This will be assessed with monitored O2 saturation, symptom of dyspnea and pulse rate during exercise)
Control(C)
Ordinary rehabilitation service of the site for 12 weeks
No interventions assigned to this group
Interventions
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Fixed respiratory rehabilitation
There are 6 step-exercise presented in the application and initial target of exercise will be set according to subject condition. After subject completes targeted exercise, next step will be started.
Responsive respiratory rehabilitation
The application provide responsive exercise program by changing type and numbers of exercise according to subject condition and exercise ability (This will be assessed with monitored O2 saturation, symptom of dyspnea and pulse rate during exercise)
Eligibility Criteria
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Inclusion Criteria
* Patients with FEV1\<80% or FVC\<80% in Pulmonary function test
* In case of COPD, post-bronchodilator FEV1 or FVC will be used.
* Exceptionally Lung Cancer patients with operation, FEV1\>80% or FVC\>80% will be permitted
* The distance walked for 6 minutes in 6-minute walk test ≥ 150 m
* Patients with android phone
* Patients who voluntarily agree to study participation and provide written informed consent form
Exclusion Criteria
* Patients with diseases that are difficult to walk or improve walking at screening
* Patients with significant diseases which are difficult to include in this study in accordance with the investigator's judgment
* Patients who are illiterate or have communication limitations
* Patients who have a difficulty to complete a questionnaire or are uncooperative due to deterioration of recognition function
20 Years
80 Years
ALL
No
Sponsors
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Ministry of Trade, Industry and Energy
UNKNOWN
Lifesemantics Corp.
INDUSTRY
Asan Medical Center
OTHER
Responsible Party
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Chang-Min Choi
associate professor
Locations
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Wonju Severance Christian Hospital
Wŏnju, Gangwon-do, South Korea
Hanyang University Guri Hospital
Guri-si, Gyeonggi-do, South Korea
KyungHee University Medical Center
Seoul, , South Korea
Asan Medical Center
Seoul, , South Korea
Smg-Snu Boramae Medical Center
Seoul, , South Korea
Countries
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References
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Cox NS, Dal Corso S, Hansen H, McDonald CF, Hill CJ, Zanaboni P, Alison JA, O'Halloran P, Macdonald H, Holland AE. Telerehabilitation for chronic respiratory disease. Cochrane Database Syst Rev. 2021 Jan 29;1(1):CD013040. doi: 10.1002/14651858.CD013040.pub2.
Kwon H, Lee S, Jung EJ, Kim S, Lee JK, Kim DK, Kim TH, Lee SH, Lee MK, Song S, Shin K. An mHealth Management Platform for Patients with Chronic Obstructive Pulmonary Disease (efil breath): Randomized Controlled Trial. JMIR Mhealth Uhealth. 2018 Aug 24;6(8):e10502. doi: 10.2196/10502.
Other Identifiers
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C2016-00568
Identifier Type: -
Identifier Source: org_study_id