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Not yet recruiting NCT06896214

The Effect of Nursing Care With Peri-Natal Loss

No phase Interventional Perinatal Loss Perinatal Grief

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Standardised nursing care intervention.
Who it may be relevant to
Registry conditions: Perinatal Loss, Perinatal Grief. Basic parameters: 18 years — 50 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effect of Standardised Nursing Care Given to Women With Peri-Natal Loss on Peri-Natal Grief, Posttraumatic Stress, Postpartum Depression

Overview

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.

Interventions

  • Other Standardised nursing care intervention
    Standardised nursing care intervention

Primary outcome measures

  • Peritanal grief scale [Time frame: at the 1st and 3rd postpartum months. The perinatal grief scale is scored between 32-160]
  • Edinburgh Postpartum depression scale [Time frame: Postpartum day 10, 1, 3 and 6 month. The Edinburgh Postpartum Depression Scale is scored between 0 and 30.]
  • Impact of Events Scale-revised [Time frame: Postpartum 1, 3 and 6 months. The Impact of Events Scale is scored between 0 and 88.]
  • Complicated grief scale [Time frame: At the 6th postpartum month.The Complicated Grief Scale is scored between 0 and 55. As the score increases, the severity of grief increases.]

Eligibility criteria

Inclusion Criteria:- To be over 18 years old

  • Being married (according to the woman's declaration)
  • Not having an existing psychiatric illness (according to the woman's declaration)
  • Not having communication problems (knowing Turkish, being literate, not having vision, speech or hearing problems, etc.)
  • Spontaneous conception
  • Singleton pregnancy
  • No substance addiction

Exclusion Criteria:Women who agreed to participate in the study but did not want to receive post-discharge care, who were hospitalised for any reason, who became pregnant again, who did not want to complete the last tests or who wanted to leave the study at any stage of the study will be excluded from the sample.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06896214 · Canan Uçakcı Asalıoğlu · No funding support was receive

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗