Skip to content

Effect of progressive change position program on lung health in patients undergoing mechanical ventilation

Effect of progressive change position program on lung health in patients undergoing mechanical ventilation

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201110237874N1
Enrollment
60
Registered
2011-12-18
Start date
2011-11-01
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mechanical ventilation pneumonia. lower respiratory infection

Interventions

Intervention 1: The Intervention group: Implementing of progressive change position program Progressive change position program is gradually putting the patient in the chair position that 3 times a da
The head of the bed at an 60 degrees and the foot of the bed an -75 degrees for 15 minutes
The head of the bed at an 75 degrees and the foot of the bed an -75 degrees for 30 minutes. In this study, the ergonomics rule is used to determine the angles of the bed. In this study, drug or chemic
Prevention
The Intervention group: Implementing of progressive change position program Progressive change position program is gradually putting the patient in the chair position that 3 times a day and in three d
In control group, do not any intervention. In this group, as intervention group, routine work is performed.

Sponsors

Vice chancellor for research, Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age between 18 to 65 years; Having oral endotracheal tube; Connected to a mechanical ventilator; Lack of previous pneumonia by chest radiography; Lack of Immunosuppressive diseases; Lack of Immunosuppressive drug; Lack of damage to the spine and being permitted to impose conditions according to intensive care specialist. Exclusion criteria: The patient died during the study; Leaving the endotracheal tube at the time of the study; The separation of mechanical ventilation during the study; The risk of pneumonia after 24 hours according to intensive care specialist.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Respiratory rate. Timepoint: Before starting the program, Half an hour after starting the program, Immediately after the end of program, An hour after the end of program. Method of measurement: Observation of values ??of respiratory rate in monitor ventilator.;Tidal volume. Timepoint: Before starting the program, Half an hour after starting the program, Immediately after the end of program, An hour after the end of program. Method of measurement: Observation of values ??of respiratory rate in monitor ventilator.;Oxygen saturation of arterial blood. Timepoint: Before starting the program, Half an hour after starting the program, Immediately after the end of program, An hour after the end of program. Method of measurement: Observation of values ??of arterial blood oxygen in pulse oximetry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNarges Baghcheghi

Hamadan University of Medical Sciences

baghcheghi@umsha.ac.ir; baghcheghinarges@yahoo.com+98 81 1251 9636

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026