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The Effect of Nursing Care With Peri-Natal Loss

NCT06896214 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 58

Last updated 2025-03-26

No results posted yet for this study

Summary

This study was planned to evaluate the effect of standardised nursing care given to women with perinatal loss using the nursing process on perinatal grief, posttraumatic stress and postpartum depression.

H01: There is no difference between pre-test, post-test and follow-up tests in terms of perinatal grief scale mean scores in the intervention group.

H02: There is no difference between pre-test, post-test and follow-up tests in terms of IES-R mean scores in the intervention group.

H03: There is no difference between pre-test, post-test and follow-up tests in terms of EPDS mean scores in the intervention group.

H04: There is no difference between the pre-test post-test and follow-up tests in terms of the mean scores of the Complicated Grief Scale in the intervention group.

* At the first encounter with women, the mean scores of PMI, IESR and EPDS will be evaluated.
* The mean EPDS score will be evaluated on the 10th postpartum day, 1st, 3rd and 6th month.
* The mean I-ESR scale score will be evaluated at postpartum 1st, 3rd and 6th month.
* At postpartum 1st and 3rd month, the mean score of PMS will be evaluated.
* At the postpartum 6th month, the mean score of the PBI scale will be evaluated.

Conditions

  • Perinatal Loss
  • Perinatal Grief

Interventions

OTHER

Standardised nursing care intervention

Standardised nursing care intervention

Sponsors & Collaborators

  • Gazi University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-04-15
Primary Completion
2025-06-30
Completion
2025-12-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06896214 on ClinicalTrials.gov