Intimate partner violence victims Not Applicable
Conditions
Interventions
Participants will be randomized 1:1 to the intervention group (usual care + multi-component plan) or the control group (usual care). A research team member who will not be directly involved in the tri
http://www.randomizer.org [accessed on 20/04/2022]). The assignment will be hidden with a password-protected file. The researchers involved in the data analysis processes will not be aware of the grou
Sponsors
University of Extremadura
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Women 2. Aged older than 18 years 3. Intimate partner violence 4. From Extremadura (the region where the project is carried out) 5. Read and signed the written informed consent
Exclusion criteria
Exclusion criteria: 1. Participants with comorbidity with other psychological problems such as depressive disorder, severe mental disorder (schizophrenia or bipolar disorders), personality disorders, and eating disorders such as anorexia or bulimia will be excluded. These psychological problems require interventions that are more specific to their nature. 2. Participants with comorbid physical problems that prevent them from carrying out adventure activities in nature 3. Women who do not know the Spanish language enough to hold a conversation 4. Patients with diabetes or cardiovascular pathology with medication or metformin will be excluded, since the results of the analyzes of the physiological variables may vary
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incremental cost-effectiveness ratio measured using EQ-5D-5L questionnaire for cost-effectiveness analysis at baseline and the first week after the last session of the intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Sociodemographic variables: sociodemographic data sheet and history of gender violence at baseline, in the first interview with participants. 2. Self-efficacy measured using the general Baessler and Schwarzer General Self-Efficacy Scale at baseline and immediately after the last session of the intervention 3. Self-esteem measured using the Rosenberg Self Esteem Scale (1965) at baseline and immediately week after the last session of the intervention 4. Body image concerns measured using the Body Shape Questionnaire (BSQ) at baseline and immediately after the last session of the intervention 5. Depression measured using the Beck Depression Inventory, Second Edition (BDI-II) at baseline and immediately after the last session of the intervention 6. Stress condition measured using the Perceived Stress Test (PSS) at baseline and immediately after the last session of the intervention 7. Stress hormonal levels measured by analysis of glucocorticoids, inflammatory and biochemical factors and using a saliva test to evaluate cortisol and the hormone DHEA, at baseline and during the first week after the last session of the intervention 8. Attendance rate assessed by an attendance sheet which will allow the researchers to know the number of female participants from the experimental group that attended at least 80% of the intervention sessions; measured immediately after each intervention session | — |
Countries
Spain
Outcome results
None listed