NCT06227013

Brief Summary

this study aims to investigate the effect of Whistleblowing intension Among Nurses by applying whistobloating education program

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
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2024

Shorter than P25 for not_applicable

Status
unknown

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 18, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

January 26, 2024

Completed
6 days until next milestone

Study Start

First participant enrolled

February 1, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2024

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2024

Completed
Last Updated

January 26, 2024

Status Verified

January 1, 2024

Enrollment Period

3 months

First QC Date

January 18, 2024

Last Update Submit

January 18, 2024

Conditions

Nurse's Role

Keywords

NursesWhistleblowing

Outcome Measures

Primary Outcomes (1)

  • easuring the change of the Whistleblowing intension of nurses

    measuring changes occure in Whistleblowing intension after applied Whistleblowing programe yo nurses

    3-months

Study Arms (2)

interventional group

EXPERIMENTAL

Whistleblowing intervention

Behavioral: Whistleblowing intervention

control group

NO INTERVENTION

no intervention

Interventions

Whistleblowing interventionBEHAVIORAL

the participated nurses will receive session about Whistleblowing

interventional group

Eligibility Criteria

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

You may qualify if:

  • licensed nurses who worked in direct contact with patients in their services had at least six month of experience in the nursing profession, agreed to participate in the study

You may not qualify if:

  • participating in any intervention program within the last 12 months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Whistleblowing

Condition Hierarchy (Ancestors)

Social BehaviorBehavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: open-label, two-arm Randomized Control Trail (RCT)
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 18, 2024

First Posted

January 26, 2024

Study Start

February 1, 2024

Primary Completion

May 1, 2024

Study Completion

June 1, 2024

Last Updated

January 26, 2024

Record last verified: 2024-01

Data Sharing

IPD Sharing
Will share

all IPD that underlie results in a publication will be shared to open data repository.

Shared Documents
STUDY PROTOCOL
Time Frame
the data will be available after publishing the trail (expected in 2024)
Access Criteria
open access