How a Resilience-Focused Intervention is Perceived by Women Subjected to Domestic Violence
EMBER-2
Exploring Resilience. A Qualitative Study of an Intervention After Intimate Partner Violence.
2 other identifiers
observational
30
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Apr 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 14, 2025
CompletedFirst Posted
Study publicly available on registry
November 19, 2025
CompletedStudy Start
First participant enrolled
April 7, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 1, 2027
April 13, 2026
April 1, 2026
7 months
November 14, 2025
April 8, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Patient experiences of EMBER
Interview questions exploring experiences and attitudes regarding the EMBER intervention
To be conducted at the time of enrollment
Secondary Outcomes (1)
Needs and resilience
to be conducted at the time of enrollment
Study Arms (1)
EMBER-intervention participants
Women subjected to intimate partner violence at the NCK outpatient clinic
Interventions
Eligibility Criteria
The participants are patients at the NCK outpatient clinic at Uppsala University Hospital, due to experiences of being subjected to intimate partner violence. Due to clinic admission criteria, the population is limited to women over 18 of age. Participants are enrolled by strategic sampling to assure a diverse sample across variables of health, age, ethnicity, socio-economy and time enrolled at the clinic.
You may qualify if:
- Enrolled in the EMBER intervention at the NCK outpatient clinic.
You may not qualify if:
- Any situation that, in the opinion of the Investigator, would compromise the safety of the patient or the quality of the data.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Uppsala University Hospital
Uppsala, Uppsala County, 75185, Sweden
Study Officials
- PRINCIPAL INVESTIGATOR
Carolina Överlien, professor
The National Centre for Knowledge on Men's Violence Against Women, Uppsala university
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 14, 2025
First Posted
November 19, 2025
Study Start
April 7, 2026
Primary Completion (Estimated)
November 1, 2026
Study Completion (Estimated)
March 1, 2027
Last Updated
April 13, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share