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How a Resilience-Focused Intervention is Perceived by Women Subjected to Domestic Violence

NCT ID: NCT07235722

Last Updated: 2025-11-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-11-30

Study Completion Date

2027-03-31

Brief Summary

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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.

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Detailed Description

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Conditions

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Shame Intimate Partner Violence Domestic Violence Exposure Resilience, Psychological

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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EMBER-intervention participants

Women subjected to intimate partner violence at the NCK outpatient clinic

Qualitative interview

Intervention Type BEHAVIORAL

A semi-structured interview

Interventions

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Qualitative interview

A semi-structured interview

Intervention Type BEHAVIORAL

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Uppsala University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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2025-04335-01

Identifier Type: OTHER

Identifier Source: secondary_id

EMBER-2

Identifier Type: -

Identifier Source: org_study_id

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