How women experience a resilience-based program after partner violence
Exploring Resilience. A Qualitative Study of an Intervention After Intimate Partner Violence.
See how a resilience-based program fits and helps women who have experienced intimate partner violence.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 30 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Uppsala University Academic / other |
| Locations | 1 site (Uppsala, Uppsala County) |
| Trial ID | NCT07235722 on ClinicalTrials.gov |
What this trial studies
This single-site observational project interviews 30 women enrolled in the EMBER intervention at the NCK outpatient clinic at Uppsala University Hospital. Researchers conduct one-hour, in-person, semi-structured interviews about each participant's life situation, self-perceived needs, resilience, and views on how the intervention met those needs. Interviews are audio-recorded, transcribed verbatim, and analyzed thematically to identify common perceptions and gaps. The goal is to understand patient experience across different stages of contact with the clinic and diverse backgrounds.
Who should consider this trial
Good fit: Women who are currently enrolled in the EMBER intervention at the NCK outpatient clinic at Uppsala University Hospital and willing to do a one-hour in-person interview are eligible.
Not a fit: Women who are not enrolled in EMBER, cannot attend in-person interviews, or whose safety would be compromised by participation are unlikely to benefit from this project.
Why it matters
Potential benefit: If successful, the findings could help the clinic better align the resilience-based program with patients' needs and improve support for women after partner violence.
How similar studies have performed: Similar qualitative studies have been used to refine services, and some resilience-based programs for intimate partner violence report promising patient-reported outcomes, though large controlled outcome trials are limited.
Eligibility criteria
Show full inclusion / exclusion 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.
Where this trial is running
Uppsala, Uppsala County
- Uppsala University Hospital — Uppsala, Uppsala County, Sweden (Recruiting)
Study contacts
- Principal investigator: Carolina Överlien, professor — The National Centre for Knowledge on Men's Violence Against Women, Uppsala university
- Study coordinator: Tove Filén, PhD-student
- Email: tove.filen@nck.uu.se
- Phone: +46721476848
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.