NCT07132450

Brief Summary

This is a prospective observational study to investigate the current clinical practice status of sedation and analgesia bundled strategies among ICU nurses

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
228

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2025

Shorter than P25 for all trials

Status
not yet recruiting

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

August 4, 2025

Completed
16 days until next milestone

First Posted

Study publicly available on registry

August 20, 2025

Completed
10 days until next milestone

Study Start

First participant enrolled

August 30, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2025

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2026

Completed
Last Updated

August 20, 2025

Status Verified

November 1, 2024

Enrollment Period

4 months

First QC Date

August 4, 2025

Last Update Submit

August 13, 2025

Conditions

Outcome Measures

Primary Outcomes (6)

  • Scale of management of pain

    A self-designed scale is used to evaluate the nurses clinical practice of the assessment, prevention and management of pain.The counting data is represented by frequency and percentiles. Items include:Use any scale to assess the patient's pain,Scale Commonly used for pain assessment,Administer analgesia to the patient in advance before nursing operations (such as venipuncture, exercise, etc.),Work in accordance with the standardized procedures for pain management in the ICU.

    Day 1

  • Scale of both spontaneous awakening tests(SATs) and spontaneous breathing tests(SBTs)

    A self-designed scale is used to evaluate the nurses clinical practice of the SATs and SBTs experiment.The counting data is represented by frequency and percentiles. Project include:Frequency of the SATs conducted every day、Perform SBTs for mechanically ventilated patients every day、Work in accordance with the standardized procedures of "Awakening and Breathing" in the ICU、Role in SATs/SBTs.

    Day 1

  • Scale of choice of sedation and analgesia

    A self-designed scale is used to evaluate the clinical practice of nurses choice of sedation and analgesia. The counting data is represented by frequency and percentiles.Projects include:Scales commonly used to evaluate the sedation status、Work in accordance with the standardized procedures for sedation management in the ICU、Maintain the minimum sedation limit for the patient or no sedation strategy、Advise intensivists to reduce the use of benzodiazepines.

    Day 1

  • Scale of delirium: assessment, prevention and management

    A self-designed scale is used to evaluate the clinical practice of nurses in the assessment, prevention, and management of patients' delirium. The counting data is represented by frequency and percentiles.Projects include:Monitor delirium for ICU patients regularly、Scales commomly used to assess delirium、Role in delirium assessment、Pay attention to the underlying causes of delirium in patients、Examinations often being paid attention to understand the causes of delirium in patients、Measures are often taken to prevent delirium、Provide earplugs to patients for use、Non-pharmacological interventions to promote patient sleep、Advise intensivists to use drugs to promote sleep、Work in accordance with the standardized procedures for delirium management in the ICU、Provide cognitive stimulation to ICU patients

    Day 1

  • Scale of early mobility and exercise

    A self-designed scale is used to evaluate the clinical practice of nurses in the e early mobility and exercise. The counting data is represented by frequency and percentiles.Projects include:Evaluate the patient's ICU-AW、Common assessment tools used for ICU-AW、Implement early activities for ICU patients、ICU activity scales used for goal-directed early activity (e.g., SOMS, PFIT, CPAx, FSS-ICU)、Types of exercises offered for ICU patients、AS a member of the ICU rehabilitation team.

    Day 1

  • Scale of family involvement and empowerment

    A self-designed scale is used to evaluate the clinical practice of nurses in the patients' family involvement and empowerment. The counting data is represented by frequency and percentiles.Projects include:Explain delirium to family members、Enhance the delirium knowledge of family members through brochures or educational materials、Involve family members in delirium management、Strategies commonly used for family participation and empowerment.

    Day 1

Secondary Outcomes (1)

  • Scale of barriers in the current practice of bundled strategies in ICU nurses

    Day 1

Study Arms (1)

ICU nurses

ICU nurses work form 28 provinces and cities in China. The inclusion criteria entailed: (1) possessing a valid nurse professional qualification certificate, and (2) having worked in an ICU for a minimum of one year. Conversely, the exclusion criteria stipulated: (1) nurses who were not working in the ICU during the study period, and (2) those in rotation or undergoing advanced training.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

ICU nurses work from 28 provinces and cities in China

You may qualify if:

  • possessing a valid nurse professional qualification certificate,
  • having worked in an ICU for a minimum of one year.

You may not qualify if:

  • nurses who were not working in the ICU during the study period
  • those in rotation or undergoing advanced training. All subjects must sign the online informed consent form before filling out the questionnaire.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

AgnosiaDeliriumEmpowerment

Condition Hierarchy (Ancestors)

Perceptual DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and SymptomsConfusionNeurocognitive DisordersMental DisordersSocial BehaviorBehavior

Central Study Contacts

weiqing Zhang Ph.D, Ph.D

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 4, 2025

First Posted

August 20, 2025

Study Start

August 30, 2025

Primary Completion

December 31, 2025

Study Completion

January 1, 2026

Last Updated

August 20, 2025

Record last verified: 2024-11