NCT07235722

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
9mo left

Started Apr 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Progress21%
Apr 2026Mar 2027

First Submitted

Initial submission to the registry

November 14, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

November 19, 2025

Completed
5 months until next milestone

Study Start

First participant enrolled

April 7, 2026

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2026

Expected
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2027

Last Updated

April 13, 2026

Status Verified

April 1, 2026

Enrollment Period

7 months

First QC Date

November 14, 2025

Last Update Submit

April 8, 2026

Conditions

Keywords

QualitativeinterviewIntimate Partner ViolenceDomestic Violencedomestic violence exposuregender-based violenceShameResilience, Psychological

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

Behavioral: Qualitative interview

Interventions

A semi-structured interview

EMBER-intervention participants

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

RECRUITING

Study Officials

  • Carolina Överlien, professor

    The National Centre for Knowledge on Men's Violence Against Women, Uppsala university

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Tove Filén, PhD-student

CONTACT

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

Locations