Impact of Lung Function Prehabilitation to Postoperative Pulmonary Complications
NCT ID: NCT06862076
Last Updated: 2025-03-06
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
40 participants
INTERVENTIONAL
2023-08-01
2024-11-12
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
PREVENTION
NONE
Study Groups
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Lung Function Prehabilitation
Participants assigned to the prehabilitation group received personalized exercise prescriptions, including aerobic training, muscle strengthening, and inspiratory muscle training with a threshold device. The prehabilitation program was conducted at the participants' homes for a minimum duration of two weeks. Adherence was monitored through logbook entries and video call evaluations to ensure correct implementation of the prescribed exercises.
Lung Function Prehabilitation
Participants assigned to the prehabilitation group received personalized exercise prescriptions, including aerobic training, muscle strengthening, and inspiratory muscle training with a threshold device. The prehabilitation program was conducted at the participants' homes for a minimum duration of two weeks. Adherence was monitored through logbook entries and video call evaluations to ensure correct implementation of the prescribed exercises.
Standard of Care
No prehabilitation is done, patients in this group received standard of care.
No interventions assigned to this group
Interventions
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Lung Function Prehabilitation
Participants assigned to the prehabilitation group received personalized exercise prescriptions, including aerobic training, muscle strengthening, and inspiratory muscle training with a threshold device. The prehabilitation program was conducted at the participants' homes for a minimum duration of two weeks. Adherence was monitored through logbook entries and video call evaluations to ensure correct implementation of the prescribed exercises.
Eligibility Criteria
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Inclusion Criteria
* scheduled for the upper abdominal surgery under general anesthesia with intraoperative mechanical ventilation
* possess adequate cognitive function to comprehend and follow instructions
* possess sufficient physical capacity to perform structured prehabilitation exercises
* express willingness to participate in the intervention program before surgery
Exclusion Criteria
* pre-existing severe pulmonary diseases such as chronic obstructive pulmonary disease (COPD)
* planned laparoscopic procedures
* history of significant neuromuscular impairment (e.g: stroke)
* declined to participate
18 Years
ALL
Yes
Sponsors
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Indonesia University
OTHER
Responsible Party
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Dita Aditianingsih
Prof. Dr. dr. Dita Aditianingsih, Sp.An-TI., Subsp.T.I.(K).
Locations
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RSUPN dr. Cipto Mangunkusumo
Jakarta Pusat, Jakarta Special Capital Region, Indonesia
Countries
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Other Identifiers
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IndonesiaUAnes049
Identifier Type: -
Identifier Source: org_study_id
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