EARLY MOBILIZATION OF INTUBETED PATIENTS IN THE INTENSİVE CARE UNİT AND THE EFFECTS OF EARLY MOBILIZATION ON RESPIRATORY PATTERN AND PATIENT HEMODYNAMICS

Sponsor
Okan University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05163379
Collaborator
(none)
25
1
2.7
9.4

Study Details

Study Description

Brief Summary

The present study was carried out as a quasi-experimental study in order to examine the effects of early mobilization of intubated patients in the intensive care unit and the effects of early mobilization on respiratory pattern and patient hemodynamics. The sample of the study consisted of 25 intubated patients monitored in the intensive care unit at in a private hospital between May 2020 and July 2021. Ethics committee approval and study permission were obtained from the hospital before starting the data collection process. Research data, descriptive data collection form, Richmond- Agitation Sedation Scale (RASS) scale, Muscle Strength Testing (Oxford Scale) and with the mobilization of the patients 45 minute in 30-60 minute including the preparation process, (1st Stage Semi Fowler position, 2nd Stage bedside sitting position, 3rd Stage in the bedside sitting position after mobilization) were registered in the Early Mobilization Follow-up Form and collected. Number and percentage calculations, repeated measurement ANOVA and Post Hoc Sheffe, LSD test analyzes were utilized in the evaluation of the data.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
25 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
EARLY MOBILIZATION OF INTUBETED PATIENTS IN THE INTENSİVE CARE UNİT AND THE EFFECTS OF EARLY MOBILIZATION ON RESPIRATORY PATTERN AND PATIENT HEMODYNAMICS
Anticipated Study Start Date :
Dec 10, 2021
Anticipated Primary Completion Date :
Feb 1, 2022
Anticipated Study Completion Date :
Mar 1, 2022

Arms and Interventions

Arm Intervention/Treatment
INTENSIVE CARE PATIENTS

EARLY MOBILIZATION OF INTUBE PATIENTS

Other: MOBILIZATION
EARLY MOBILIZATION OF INTUBE PATIENTS AND ITS EFFECTS OF MOBILIZATION

Outcome Measures

Primary Outcome Measures

  1. EARLY MOBILIZATION OF INTUBE PATIENTS AND THE EFFECTS OF EARLY MOBLIZATION ON RESPIRATORY PATTERN AND PATIENT HEMODYNAMICS [ONE DAY]

    HEMODYNAMIC EFFECTSRESPIRATORY PATTERN, BLOOD GAS ANALYSISZ

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 18 years and over,

  • Hemodiamic stability (OCD >60, OCD <120, respiratory rate <35, SpO2 >90),

  • Areas of >3/5 (Oxford scale) and above on the lower limbs with areas of secure support,

  • The patient scores 0 (awake and calm) on the Richmond Agitation Sedation Scale (RASS),

  • PaO2 / FiO2 ≥300,

  • Body temperature below 38 degrees,

  • Platelet count ≥20,000 cells / mm3,

  • Having blood sugar of 60-360 mg/dl,

  • Having arterial monitoring,

  • Patient with 30% FiO2 due to mechanical ventilator,

  • Those with mechanical ventilator-dependent ventilation method (mode) PASB,

  • Patient with a PEEP value of 5 due to mechanical ventilator,

  • Patient with a PASB value of 10 connected to a mechanical ventilator,

  • A sample accepted by the patient who voluntarily agreed to participate in the study was approximated from the patient.

Exclusion Criteria:
  • Patients under the age of 18,

  • Those with hemodynamic instability (OCD <60 mmHg, OCD >120 mmHg, breath rate >35, SpO2 <90),

  • Those who do not have secure unsupported sitting balance and have a score of >3/5 (Oxford scale) in the lower limbs,

  • Patients whose Richmond agitation sedation scale (RASS) is between +1 and +4 points, and patients with a score between -1 and -5,

  • Those with arrhythmia,

  • Patients without arterial monitoring,

  • Patients whose FiO2 percentage is not 30% in patients on mechanical ventilator,

  • Patients who do not have ventilation method (mod) PASB in patients on mechanical ventilator,

  • Patients who do not have a PEEP value of 5 in patients on mechanical ventilators,

  • Patients who do not have a PASB value of 10 in patients on mechanical ventilators,

  • Those with neurological and orthopedic contraindications,

  • Patients who could not get approval from the relatives of the patients who did not accept to participate in the study were excluded from the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Gürkan ÇAMOK Istanbul İ̇stanbul Turkey 34959

Sponsors and Collaborators

  • Okan University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Gürkan ÇAMOK, Nursing Graduate Student, Okan University
ClinicalTrials.gov Identifier:
NCT05163379
Other Study ID Numbers:
  • GURKANCAMOK
First Posted:
Dec 20, 2021
Last Update Posted:
Dec 20, 2021
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Dec 20, 2021