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Effectiveness of an advanced nursing care for severe features of preeclampsia integrative simulation-based training program to enhance competency and self-efficacy of the nurse midwives.

Development of an advanced nursing care for severe features of preeclampsia integrative simulation-based training program to enhance competency and self-efficacy of the nurse midwives: a mixed-method research.

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260702003
Enrollment
60
Registered
2026-07-02
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Severe features of preeclampsia stimulation, nurse midwives, preeclampsia with severe features, eclampsia, HELLP syndrome, chronic hypertension with superimposed preeclampsia, obstetric emergencies

Interventions

Pre-intervention (pre-test
T0): All 30 nurse midwives of experimental groups complete baseline assessments of knowledge, skills, and self-efficacy. Implementation: The experimental group receives the ANC-SFP-ISimPro (Weeks 1-2
10 nurse midwives for the experimental group are learning in the scenario for the purpose of a training course of ANC-SFP-ISimPro. -Health educational session. The nurse midwives received a brief ori
Experimental Procedure/Surgery,No Intervention No treatment
Experimental group (ANC-SFP-ISimPro),Control group

Sponsors

Chiangrai College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Registered nurses with valid midwifery licenses, currently practicing in the specified units. 1. Aged 18 years or older. 2. Work in the obstetrics department, which comprises three subunits: the antenatal care unit, the delivery room, and the postpartum ward. 3. Hold a nursing and midwifery license. 4. Willing to voluntarily participate in the research project.

Exclusion criteria

Exclusion criteria: 1. No internet-connected device. 2. Experience in obstetrics care less than 1 year.

Design outcomes

Primary

MeasureTime frame
competency and self-efficacy pre-intervention (T0), Post-intervention (T1, immediately after 2 week training) and 8-week follow-up (T2, at week 11 interval of 8 weeks post-training). competency (knowledge and skill) score and self-efficacy score

Secondary

MeasureTime frame
Satisfation At week 11 after the end of training ANC-SFP-ISimPro Satisfation score

Countries

Thailand

Contacts

Public ContactBoontharika Wongkom

Faculty of nursing, Burapha University

joywongkom8@gmail.com0832096592

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026