NCT07754903

Brief Summary

New nurses often find it difficult to adjust when they start working in fast-paced, high-pressure trauma units, and many leave their jobs within the first two years. This study looks at whether a two-day training programme, called Basic Trauma Training (BTT), helps newly graduated nurses in Saudi trauma hospitals feel more confident, satisfied and engaged in their work, and more likely to stay in the nursing profession. The study takes place at two trauma hospitals in Saudi Arabia. Because it is not practical to randomly assign nurses to groups in this real-world hospital setting, the study compares an earlier group of new nurses, who receive standard hospital orientation only, with a later group, who receive standard orientation plus the two-day BTT training. Both groups complete questionnaires before and after their orientation or training period, answering questions about job satisfaction, engagement, stress and their plans to stay in the role. The study also looks at actual staff retention using hospital employment records at 6 and 12 months. Nurses in the comparison group are offered the BTT training later, once their part of the study is complete, so that everyone has the chance to take part in the training.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
128

participants targeted

Target at P50-P75 for not_applicable

Timeline
5mo left

Started Sep 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

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 5, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 10, 2026

Completed
22 days until next milestone

Study Start

First participant enrolled

September 1, 2026

Expected
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2027

1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 31, 2027

Last Updated

August 10, 2026

Status Verified

August 1, 2026

Enrollment Period

4 months

First QC Date

August 5, 2026

Last Update Submit

August 5, 2026

Conditions

Keywords

newly graduated nursestrauma nursingworkforce sustainabilitytransition shockjob demands-resources modelSaudi Arabiaquasi-experimental

Outcome Measures

Primary Outcomes (1)

  • Workforce Sustainability (Composite Index)

    A formative composite index of four equally weighted, standardised (z-score) components: job satisfaction (Michigan Organizational Assessment Questionnaire Job Satisfaction Subscale, MOAQ-JSS, 3 items, 7-point Likert), work engagement (Utrecht Work Engagement Scale, UWES-9, 0-6 frequency scale), personal burnout (Copenhagen Burnout Inventory, CBI-PB, 6 items, 0-100 scale, reverse scored), and retention intention (validated instrument, to be finalised). Each component is standardised using the pooled baseline mean and SD across both arms at T0, and the four standardised components are averaged.

    Baseline (T0) and 4-6 weeks post-intervention/orientation (T1)

Secondary Outcomes (1)

  • Job Satisfaction

    Baseline (T0) and 4-6 weeks post-intervention/orientation (T1)

Study Arms (2)

Intervention (BTT)

EXPERIMENTAL

Participants receive the Basic Trauma Training (BTT) programme, a two-day (14 contact-hour) simulation-based educational intervention, in addition to standard institutional orientation

Behavioral: Basic Trauma Training (BTT) Programme

Comparator (Standard Orientation)

EXPERIMENTAL

Participants receive standard institutional orientation only (approximately five days of general clinical induction, without trauma-specific structured training). BTT is offered to this group after their follow-up (T1) assessment.

Other: Standard Institutional Orientation

Interventions

Standard existing onboarding programme for newly employed nursing staff, comprising approximately five days of general clinical induction without trauma-specific structured training. Content and duration are documented at baseline to characterise the comparator condition precisely.

Comparator (Standard Orientation)

A structured two-day, 14-contact-hour educational programme comprising five modules: trauma systems and primary survey principles; advanced trauma assessment and clinical reasoning; critical trauma interventions and patient safety; interprofessional communication and team leadership; and psychological preparedness, peer support and self-care. Delivered via didactic teaching, high-fidelity simulation using the PEARLS debriefing framework, and facilitated reflective discussion.

Intervention (BTT)

Eligibility Criteria

Age21 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Saudi Commission for Health Specialties (SCFHS) licensure
  • Less than 12 months of post-licensure clinical experience at baseline
  • Current direct patient-facing employment in a trauma-related intensive care unit at King Saud Medical City or Northern Medical Tower
  • Willing and able to provide written informed consent

You may not qualify if:

  • More than 12 months of post-licensure clinical experience
  • Employment outside trauma-related ICU settings
  • Agency or temporary staffing status
  • Extended leave during the intervention or data-collection period
  • Prior formal trauma-specific training (ATCN, TNCC) before enrolment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

King Saud Medical City

Riyadh, Ulaishah / Shumaisi, 12746, Saudi Arabia

Location

Related Publications (4)

  • Aggar C, Bloomfield J, Thomas TH, Gordon CJ. Australia's first transition to professional practice in primary care program for graduate registered nurses: a pilot study. BMC Nurs. 2017 Mar 23;16:14. doi: 10.1186/s12912-017-0207-5. eCollection 2017.

    PMID: 28344514BACKGROUND
  • Lyu XC, Huang SS, Ye XM, Zhang LY, Zhang P, Wang YJ. What influences newly graduated registered nurses' intention to leave the nursing profession? An integrative review. BMC Nurs. 2024 Jan 19;23(1):57. doi: 10.1186/s12912-023-01685-z.

    PMID: 38243209BACKGROUND
  • Rush KL, Janke R, Duchscher JE, Phillips R, Kaur S. Best practices of formal new graduate transition programs: An integrative review. Int J Nurs Stud. 2019 Jun;94:139-158. doi: 10.1016/j.ijnurstu.2019.02.010. Epub 2019 Feb 26.

    PMID: 30965203BACKGROUND
  • Duchscher JE. Transition shock: the initial stage of role adaptation for newly graduated registered nurses. J Adv Nurs. 2009 May;65(5):1103-13. doi: 10.1111/j.1365-2648.2008.04898.x. Epub 2009 Dec 9.

    PMID: 19183235BACKGROUND

Related Links

MeSH Terms

Conditions

Burnout, Professional

Condition Hierarchy (Ancestors)

Occupational StressOccupational DiseasesBurnout, PsychologicalStress, PsychologicalBehavioral SymptomsBehavior

Study Officials

  • Abdulaziz L Alanazi

    Lincoln University College

    PRINCIPAL INVESTIGATOR
  • Faridah M Said

    Lincoln University College

    STUDY DIRECTOR

Central Study Contacts

Abdulaziz Sultan L. Alanazi

CONTACT

Faridah Mohd Said Dr.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Masking Details
Data management and statistical analysis are conducted with arm labels masked to the analysis team until primary models have been fitted, to reduce analytic bias despite the inability to mask participants or facilitators to the intervention itself.
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Model Details: Two-site, non-equivalent comparison-group quasi-experimental design. Allocation is by successive intake cohort within each site rather than by randomisation, so that study arm is not confounded with site; both participating sites contribute nurses to both the comparator and intervention arms.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Mr.

Study Record Dates

First Submitted

August 5, 2026

First Posted

August 10, 2026

Study Start (Estimated)

September 1, 2026

Primary Completion (Estimated)

January 1, 2027

Study Completion (Estimated)

January 31, 2027

Last Updated

August 10, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Individual participant data (IPD) will not be shared with other researchers. The study involves sensitive health information collected from psychiatric nurses and patients in Saudi Arabia, and the informed consent process does not include permission for public sharing of de-identified participant-level data. To protect participant confidentiality and comply with institutional ethical requirements, applicable Saudi data protection regulations, and the approvals granted by the relevant Institutional Review Boards (IRBs), only aggregated study results will be published. Researchers interested in additional information may contact the Principal Investigator to discuss the availability of study materials, including the study protocol, statistical analysis plan, and data collection instruments, where appropriate.

Locations