Shame, Resilience and Well-being After Intimate Partner Violence: an Intervention Study With Replicated Single-Subject Design.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUppsala University

About this trial

The EMBER protocol is a health care method that is designed to increase resilience, in order to improve well-being and overall health in women who have experienced violence by a partner. This study explores whether the EMBER intervention works in this way. Eight participants will take part in the EMBER program and complete questionnaires every week during the intervention. The researchers will compare the timeline for the intervention to how resilience levels change. They will also check whether changes in resilience are linked to changes in health and well-being.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

subjected to IPV within 2 years prior to enrollment

capable of completing questionnaires using a mobile phone

intention to complete intervention

identifies as female

Disqualifiers

ongoing severe IPV

ongoing severe substance use

psychosis

moderate to severe suicidality

Trial design

Design model

Single group

Treatments tested in this trial

  • Resilience enhancing intervention, individual format

    Other intervention

    A 4-step, Resilience-focused intervention based on the Resilience Portfolio Model, administered in individual format.

  • Resilience enhancing intervention, group format

    Other intervention

    A 4-step, Resilience-focused intervention based on the Resilience Portfolio Model, administered in group format.

Treatment groups

8 Participants
are divided into 1 treatment group
Group A: EMBER interventionExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Resilience - Psychological Endurance

The self assessment questionnaire Psychological Endurance Scale (range 6-24, higher value indicates higher endurance) is completed bi-weekly using a mobile application. Data will be analyzed with a combination of visual and statistical analyses.

Time frame
Bi-weekly from enrollment 2-6 weeks prior to start of intervention, to completion of the intervention (intervention phase A and/or C). Follow-up 6 weeks post-intervention.
2

Resilience - Subjective Social Support

The Oslo Subjective Social Support Scale - 3 items (range 3-14, higher value indicates higher level of social support) is completed bi-weekly using a mobile application. Data will be processed using a combination of visual and statistical analyses.

Time frame
Bi-weekly from enrollment 2-6 weeks prior to start of intervention to completion of the intervention (intervention phase A and/or C). Follow-up 6 weeks post-intervention.
3

Resilience - Meaning Making

The MAPS - Meaningfulness subscale (range 5-25, higher value indicating higher meaningfulness) is completed by the subjects bi-weekly. Data is processed using a combination of statistical and visual analyses.

Time frame
Bi-weekly from enrollment 2-6 weeks prior to start of the intervention, to completion of the intervention (intervention phase A and/or C). Follow-up 6 weeks post-intervention.

Secondary outcomes

1

Health

General, Somatic, Mental, Social and Sexual health is measured by 5 questions regarding subjective health the past week which are administered to the subject using a mobile application. The subject grades ones health on a visuoanalogue scale ranging from -10 to +10. The range on the total scale is thus -50 to +50, subscales -10 to +10. Higher value indicates better health. Data is processed using a combination in visual and statistical analyses.

Time frame
Bi-weekly from enrollment 2-6 weeks prior to the intervention, to completion of the intervention (intervention phase A and/or C). Follow-up 6 weeks post-intervention.
2

Shame

Shame is measured using the External and Internal Shame Scale (EISS; range 0.00-4.00, higher value indicating higher levels of shame), administered to patients using a mobile application. Data is processed using a combination of statistical and visual analyses.

Time frame
Bi-weekly from enrollment 2-6 weeks prior to start of the intervention, to completion of the intervention (intervention phase A and/or C). Follow-up 6 at weeks post-intervention.
3

Well-Being

Well-being is measured bi-weekly using the Questionnaire on Well-Being (QWB, range 0-72, higher value indicating more wellbeing). Data is processed using a combination of statistical and visual analyses.

Time frame
Bi-weekly from enrollment 2-6 weeks prior to start of the intervention, to completion of the intervention (intervention phase A and/or C). Follow-up at 6 weeks post-intervention.

Other outcomes

Sponsors and contacts

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