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Effectiveness of a Nursing Intervention for Nurses Have Experienced Trauma: a Study Based on Swanson's Caring Theory

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Yonsei University

Status

Completed

Conditions

Nurses Who Have Experienced Trauma

Treatments

Other: The trauma recovery nursing intervention program

Study type

Interventional

Funder types

Other

Identifiers

NCT04989582
Y-2019-0083

Details and patient eligibility

About

This study aimed to (1) develop an internet-based psychiatric nursing intervention, based on Swanson's theory of caring, and (2) examine its effects on functional health, resilience, social support, post-traumatic stress, depression, and anxiety.

This study was a randomized clinical trial(RCT) study with repeated measures to identify the effectiveness of an internet-based psychiatric nursing intervention. Participants were evaluated at the following time points: pre-test (pre), post-test (post-test 1, immediately after intervention), and follow-up (post-test 2, one month after the intervention) to assess the sustainability of the internet-based psychiatric nursing intervention.

Of the 112 women who enrolled in the study, 10 dropped out before post-test 1, resulting in 102 participants who completed all interventions and surveys.

Enrollment

112 patients

Sex

All

Ages

23 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. nurse aged from 23 to 40 years
  2. a PTS score of 64 or lower on the PTSD checklist for DSM-5 (PCL-5) developed by Weathers et al., revised by Weathers et al., and translated into Korean by Kim et al.,
  3. nurse who can access the program through a computer or mobile
  4. nurse who understand the purpose of the research and voluntarily agree to participate in the research.

Exclusion criteria

  1. presence of psychiatric conditions with hallucinations and delusions
  2. diagnosis of an intellectual disability that would make understanding the intervention procedure difficult. Although a standard cut-off was not present in the PCL-5, women who exceeded 80% (64 points) of the total score were excluded to rule out high-risk women with severe trauma.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

112 participants in 2 patient groups

Nursing intervention
Experimental group
Description:
Nurses randomly assigned by applying a random selection method
Treatment:
Other: The trauma recovery nursing intervention program
No intervention
No Intervention group
Description:
Nurses randomly assigned by applying a random selection method

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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