The De-Morton Mobility Index Turkish Version in Intensive Care Patients

Critical Care Clinical Trial

Official title:

Construct Validity and Test-Retest Reliability of The De-Morton Mobility Index Turkish Version in Intensive Care Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05196997
• Other study ID #: DM111
• Status: Completed
• Start date: April 1, 2018
• Est. completion date: February 20, 2019

Study information

• Verified date: January 2022
• Source: Izmir Katip Celebi University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

De Morton Mobility Index is recommended for the evaluation of mobility in the evidence-based guidelines, in patients in intensive care units. The aim of our study is to examine the validity and reliability of the Turkish version of the De Morton Mobility Index in patients hospitalized in the respiratory intensive care unit.

Description:

De Morton Mobility Index is recommended for the evaluation of mobility in the evidence-based guidelines, in patients in intensive care units. The aim of our study is to examine the validity and reliability of the Turkish version of the De Morton Mobility Index in patients hospitalized in the respiratory intensive care unit. Patients aged 18 years and over who were discharged from the ICU were included in our study. We used De-Morton Mobility Index, Bartel Index, Katz Activities of Daily Living Rating Scale and MRC Muscle Strength Test for convergent validity. De-Morton Mobility assessment for test-retest reliability was performed again on the 1st day of the patient's service.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 150
• Est. completion date: February 20, 2019
• Est. primary completion date: February 20, 2019
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• staying in intensive care unit for at least 24 hours
• able to cooperate
• being clinically stable for mobility assessment

Exclusion Criteria:

• the presence of neurological disease
• the presence of orthopedic problems such as fractures
• the presence of metastases
• the presence of cardiorespiratory instability

Related Conditions & MeSH terms

• Critical Care
• Function
• Mobility

Intervention

Other:
• Mobility and Functional Assessments
The first evaluation was made on the day the patient was discharged from the intensive care unit. DEMMI, Bartel Index, Katz Activities of Daily Living Rating Scale and MRC Muscle Strength Test were performed to the patient, respectively. De-Morton Mobility assessment for test-retest reliability was performed again on the 1st day of the patient's service.

Locations

Country	Name	City	State
Turkey	Ilknur Naz Gürsan	Izmir

Sponsors (1)

Lead Sponsor	Collaborator
Izmir Katip Celebi University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mobility Assessment	De Morton Mobility Index: It consists of a total of 15 mobility items. The total score ranges from 0-100, with 0 indicating poor mobility and 100 indicating high mobility	15 minutes
Secondary	Functional independence measurement	The Barthel index: It includes 10 items: nutrition, bathroom, personal care, dressing, toilet use, mobility on flat surfaces (immobile, wheelchair use, walking with assistance or independently), transfer (transfer from wheelchair to bed and vice versa), climbing stairs, bowel and bladder continence. It is scored between 0-100. 0; fully independent, 100; means fully independent.	5 minutes
Secondary	Assessment of daily living activities	Katz Index: The index includes basic parameters of daily living activities such as bathing, dressing, toilet, transfer, urine and stool control, nutrition. The scoring of the index varies in the range of 0-6. Higher scores indicate higher independence	5 minutes
Secondary	Muscle Strength	Medical Research Council scale: It includes muscle strength test of six muscle groups. Scoring ranges from 0 to 5 in each muscle group. The maximum score is 60, and a score below 48 indicates significant muscle weakness	10 minutes