Study Results
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View full resultsBasic Information
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COMPLETED
NA
64 participants
INTERVENTIONAL
2022-07-25
2024-02-16
Brief Summary
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By analyzing the difference from the existing postoperative pulmonary rehabilitation, the investigators would like to propose a new pulmonary tele-rehabilitation protocol.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Tele-rehabilitation group
The Tele-rehabilitation group performs 12 training sessions during four weeks. (3 sessions/week)
Pulmonary Tele-Rehabilitation
12 supervised training sessions via a specific mobile messenger during four weeks. (3 sessions/week)
Control group
The control group receives usual care with only one educational session.
Control (Education)
Usual care with only one educational session.
Interventions
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Pulmonary Tele-Rehabilitation
12 supervised training sessions via a specific mobile messenger during four weeks. (3 sessions/week)
Control (Education)
Usual care with only one educational session.
Eligibility Criteria
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Inclusion Criteria
2. men and women the age ≥65 years.
3. A person who understands the course of the clinical trial and signs the informed consent form.
Exclusion Criteria
2. Patients who cannot test bioimpedance analysis due to the insertion of artificial pacemakers and defibrillators
3. A person who has difficulty judging himself/herself due to dementia, etc
4. Those enrolled in other clinical trials
5. A person deemed inappropriate to participate in this clinical trial under the judgement of the investigator.
6. A person who cannot use mobile messenger
65 Years
ALL
No
Sponsors
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National Research Foundation of Korea
OTHER
Pusan National University Hospital
OTHER
Responsible Party
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Principal Investigators
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Sang Hun Kim, M.D.,Ph.D.
Role: STUDY_DIRECTOR
Pusan National University Hospital
Locations
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PusanNUH
Pusan, , South Korea
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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2205-033-114
Identifier Type: -
Identifier Source: org_study_id
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