How a Resilience-Focused Intervention is Perceived by Women Subjected to Domestic Violence
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: Qualitative interview.
- Who it may be relevant to
- Registry conditions: Shame, Intimate Partner Violence, Domestic Violence Exposure, Resilience, Psychological. Basic parameters: from 18 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
- Sweden
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Exploring Resilience. A Qualitative Study of an Intervention After Intimate Partner Violence.
Overview
At Uppsala University Hospital, there is an outpatient clinic for women subjected to intimate partner violence. In order to explore how patients experience the biopsychosocial resilience-based intervention in use at the clinic and how well the intervention fits the needs of the patients, 30 patients from different stages of their contact at the clinic and with diverse life situations and background are enrolled. The researchers will carry out individual in-person interviews, each lasting approximately 60 minutes, based on a semi-structured set of questions. The questions concern the participant´s life situation, resilience and self-perceived needs, how well the intervention has met those needs and how it was perceived by the participant. The interviews are audio-recorded and transcribed verbatim for thematic analysis.
Interventions
- Behavioral Qualitative interview
A semi-structured interview
Primary outcome measures
- Patient experiences of EMBER [Time frame: To be conducted at the time of enrollment]
Secondary outcome measures (1)
- Needs and resilience [Time frame: to be conducted at the time of enrollment]
Eligibility criteria
Inclusion criteria
- Enrolled in the EMBER intervention at the NCK outpatient clinic.
Exclusion criteria
- Any situation that, in the opinion of the Investigator, would compromise the safety of the patient or the quality of the data.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Other
Study locations
Sweden · 1 center
- Uppsala University Hospital — Uppsala
Identifiers
NCT: NCT07235722 · EMBER-2 · 2025-04335-01