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
30 participants
INTERVENTIONAL
2017-10-10
2018-02-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Inspiratory muscle training group
Patients will continue 8 weeks, 5 days, 2 times 15 minutes training program with %30 MIP at home.
inspiratory muscle training
The treatment group received IMT. Patients were trained using an inspiratory threshold-loading device
control group
Patients will continue 8 weeks, 5 days, 2 times 15 minutes training program with 9 cmH2O pressure at home.
No interventions assigned to this group
Interventions
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inspiratory muscle training
The treatment group received IMT. Patients were trained using an inspiratory threshold-loading device
Eligibility Criteria
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Inclusion Criteria
* NYHA functional class I-IV
* MIP pressure \<80 cm h2O
Exclusion Criteria
* Conditions which can limit the assessments
* Insufficient cooperation
18 Years
80 Years
ALL
No
Sponsors
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Biruni University
OTHER
Istanbul University
OTHER
Responsible Party
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Goksen Kuran Aslan
Associated Proff.
Principal Investigators
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Goksen Kuran Aslan
Role: STUDY_DIRECTOR
Istanbul University
Locations
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Istanbul University
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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BuketA
Identifier Type: OTHER
Identifier Source: secondary_id
GAslan
Identifier Type: -
Identifier Source: org_study_id
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