NCT02804516

Brief Summary

Despite evidence to support early mobilization(EM)for critically ill patients,current status in Chinese ICUs is unknown.Understanding current practice patterns and challenges is essential to inform future research and strategies.

Trial Health

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,000

participants targeted

Target at P75+ for not_applicable

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 10, 2016

Completed
7 days until next milestone

First Posted

Study publicly available on registry

June 17, 2016

Completed
14 days until next milestone

Study Start

First participant enrolled

July 1, 2016

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2016

Completed
Last Updated

June 17, 2016

Status Verified

June 1, 2016

Enrollment Period

1 month

First QC Date

June 10, 2016

Last Update Submit

June 14, 2016

Conditions

Outcome Measures

Primary Outcomes (1)

  • the implementation rates for early mobility

    the application of physical activity within the first 2 to 5 days of critically illness or injury

    within the first 2 to 5 days of critically illness or injury

Study Arms (2)

the nurse did early mobilization

EXPERIMENTAL

the nurses know and do what is the early mobilization in ICU

Behavioral: the nurse did early mobilization

the nurse do not do early mobilization

EXPERIMENTAL

the nurses do not know and do what is the early mobilization in ICU

Behavioral: the nurse do not do early mobilization

Interventions

the nurses know and do what is the early mobilization in ICU

the nurse did early mobilization

the nurses do not know and do what is the early mobilization in ICU

the nurse do not do early mobilization

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may not qualify if:

  • pediatric ICUs

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Southeast University, China

Study Record Dates

First Submitted

June 10, 2016

First Posted

June 17, 2016

Study Start

July 1, 2016

Primary Completion

August 1, 2016

Last Updated

June 17, 2016

Record last verified: 2016-06