Меню
Набор скоро начнётся NCT07618754

Shame, Resilience and Well-being After Intimate Partner Violence: an Intervention Study With Replicated Single-Subject Design.

Без фазы С лечением Intimate Partner Violence Resilience, Psychological

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Resilience enhancing intervention, individual format, Resilience enhancing intervention, group format.
Кому может быть актуально
Состояния в реестре: Intimate Partner Violence, Resilience, Psychological. Базовые параметры: от 18 лет · Женщины.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Швеция
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

Не всё понятно в терминах? Прочитайте наш гид для пациентов →

Обзор

The EMBER protocol is a health care method that is designed to increase resilience, in order to improve well-being and overall health in women who have experienced violence by a partner. This study explores whether the EMBER intervention works in this way. Eight participants will take part in the EMBER program and complete questionnaires every week during the intervention. The researchers will compare the timeline for the intervention to how resilience levels change. They will also check whether changes in resilience are linked to changes in health and well-being.

Подробное описание

Intimate partner violence (IPV) is a global problem with complex consequences in society as well as for the victim/survivor. The EMBER-protocol was developed at National Center for Knowledge on Men´s violence against Women, Uppsala University, Sweden. The purpose of the protocol is to provide women who have been subjected to IPV with support and tools for empowerment and improving resilience, thereby improving health and well-being. In this study with replicated single-case design, 8 patients will complete questionnaires bi-weekly while taking part of the intervention, starting from their very first contact with the clinic. The questionnaires are completed using a mobile application. Data will be processed using a combination of visual and statistical analysis, in order to examine how interventions intended to improve resilience, changes in resilience measures and changes in well-being and health relate to each other temporally.

Вмешательства

  • Другое Resilience enhancing intervention, individual format
    A 4-step, Resilience-focused intervention based on the Resilience Portfolio Model, administered in individual format.
  • Другое Resilience enhancing intervention, group format
    A 4-step, Resilience-focused intervention based on the Resilience Portfolio Model, administered in group format.

Первичные конечные точки

  • Resilience - Psychological Endurance [Срок оценки: Bi-weekly from enrollment 2-6 weeks prior to start of intervention, to completion of the intervention (intervention phase A and/or C). Follow-up 6 weeks post-intervention.]
  • Resilience - Subjective Social Support [Срок оценки: Bi-weekly from enrollment 2-6 weeks prior to start of intervention to completion of the intervention (intervention phase A and/or C). Follow-up 6 weeks post-intervention.]
  • Resilience - Meaning Making [Срок оценки: Bi-weekly from enrollment 2-6 weeks prior to start of the intervention, to completion of the intervention (intervention phase A and/or C). Follow-up 6 weeks post-intervention.]
Вторичные конечные точки (3)
  • Health [Срок оценки: Bi-weekly from enrollment 2-6 weeks prior to the intervention, to completion of the intervention (intervention phase A and/or C). Follow-up 6 weeks post-intervention.]
  • Shame [Срок оценки: Bi-weekly from enrollment 2-6 weeks prior to start of the intervention, to completion of the intervention (intervention phase A and/or C). Follow-up 6 at weeks post-intervention.]
  • Well-Being [Срок оценки: Bi-weekly from enrollment 2-6 weeks prior to start of the intervention, to completion of the intervention (intervention phase A and/or C). Follow-up at 6 weeks post-intervention.]

Критерии участия

Критерии включения

  • subjected to IPV within 2 years prior to enrollment
  • capable of completing questionnaires using a mobile phone
  • intention to complete intervention
  • identifies as female

Критерии исключения

  • ongoing severe IPV
  • ongoing severe substance use
  • psychosis
  • moderate to severe suicidality
  • ongoing psychological intervention in other facility

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

Швеция · 1 центр
  • Uppsala University Hospital — Uppsala

Идентификаторы

NCT: NCT07618754 · EMBER-4

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗