Individualized Grief Support With Swanson Model

Официальное название

Evaluation of the Effectiveness of Individualized Grief Support Based on the Swanson Caring Model in Women Experiencing Pregnancy Loss

Обзор

This study aims to examine the effects of individualized grief support for women experiencing pregnancy loss. The research, which will be conducted at Süleyman Demirel University, is a mixed-method design and includes both phenomenological qualitative analysis and randomized controlled quantitative trials. The sample will include 48 women; those with severe depression will be excluded. Quantitative data will be analyzed using SPSS, and qualitative data will be analyzed using content analysis.

Подробное описание

Pregnancy loss is a traumatic experience that leaves deep marks on women's lives. The grieving process that women experience during this period varies according to individual differences. The aim of this study is to examine the effects of individualized grief support for women who have experienced pregnancy loss. By addressing the emotional and psychological challenges women face after pregnancy loss, the study seeks to explore how the most appropriate support and care can be provided.

The sample of the study will consist of women who have experienced pregnancy loss at Süleyman Demirel University Research and Training Hospital, Department of Obstetrics and Gynecology. The power analysis of the study was conducted using the GPower 3.1.9.6 (Franz Faul, Universitaet Kiel, Germany) program, and the sample size was calculated as n=24+24=48. Women who obtain a very high score (14+) on the depression subscale of the Depression-Anxiety-Stress Scale will not be included in the study due to pathological findings.

This research will be conducted as a mixed-method study incorporating both qualitative and quantitative methods. In the qualitative part of the study, a phenomenological design, which is suitable for the nature of the research, will be used. The quantitative part will be conducted as a randomized controlled trial. Quantitative data are planned to be analyzed using the SPSS (Statistical Program for Social Sciences) 26.0 statistical analysis package. Qualitative data will be analyzed through content analysis using a software program commonly utilized for qualitative research.

Вмешательства

• Другое Assigned Interventions
  Semi-structured interviews will be conducted with women who have experienced pregnancy loss, and their experiences and grieving processes will be examined phenomenologically. In the 3rd, 4th, and 5th interviews, based on the findings obtained from the qualitative data, grief counseling based on the Swanson care model will be provided to the women, and they will be provided with nursing care and grief support.

Первичные конечные точки

• Personal Information Form (Pre-Test) [Срок оценки: At baseline (prior to intervention)]
• Sociodemographic Characteristics Form [Срок оценки: Baseline (pre-intervention)]
• Perinatal Grief Scale (PGS) Score [Срок оценки: Baseline (pre-intervention)]
• Depression Anxiety Stress Scale-21 (DASS-21) [Срок оценки: Baseline (pre-intervention)]
• Bereavement Brochure [Срок оценки: Immediately post-intervention]
• Semi-Structured Interview [Срок оценки: 1 week]
• Swanson-Based Grief Counseling (First Session) [Срок оценки: 3 weeks]
• Swanson-Based Bereavement Counseling (Second Session) [Срок оценки: 2nd month]
• Swanson-Based Bereavement Counseling (Third Session) + Post-Test Data Collection [Срок оценки: 3rd month]

Критерии участия

Критерии включения

• Aged 18 years and above,
• Literate,
• Able to understand and speak Turkish,
• Desired and planned pregnancies
• No diagnosed psychiatric illness,
• No hearing or mental disabilit

Критерии исключения

• Women who experienced pregnancy loss after infertility treatment
• Women who received psychological support during the process
• Women who scored very high on the DAS scale
• Women who withdrew from the study at any stage
• Women who did not complete the data collection forms will be excluded from the study.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение

Рандомизированное

Модель

Параллельные группы

Маскирование

Двойное слепое

Основная цель

Фундаментальное исследование

Центры проведения

Turkey (Türkiye) · 1 центр

• Suleyman Demirel University — Isparta

Идентификаторы

NCT: NCT07333391 · SDUSuleyman

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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