Domestic Violence Clinical Trial
Official title:
Evaluating the Clinical Utility and Client Acceptability of Video Intervention
NCT number | NCT03658499 |
Other study ID # | 1245130-1 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | July 26, 2018 |
Est. completion date | July 1, 2019 |
Verified date | November 2020 |
Source | University of Nevada, Reno |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Intimate partner violence (IPV) is a common occurrence in the U.S. Victims of IPV are at an elevated risk of experiencing a variety of physical and mental health consequences, which frequently co-occur and act synergistically, placing victims at a higher risk for revictimization. Experts recommend that interventions for victims of IPV focus on helping victims attain more balanced emotions and behaviors, rather than treating specific nosologies. One transdiagnostic treatment, Dialectical Behavior Therapy (DBT), focused on helping individuals gain more balanced emotions and behaviors, has shown success in treating victims of IPV. However, the DBT for IPV treatment protocol is not without it's limitations. Specifically, clients may need additional exposure to the skills and concepts taught in the treatment. Yet, additional exposure to the skills facilitated though a therapist is difficult to do given the limited budgets for services for victims of IPV and the client provider gap. In order to address the client provider gap, increase exposure to the skills, and to increase skills acquisition and generalization, video intervention adjuncts (VIAs) have been developed to serve as treatment adjuncts for the DBT for IPV skills group. The objective of the current study is to conduct a randomized control trial examining the treatment utility and participant acceptability of the two-day DBT for IPV skills group plus the VIAs versus treatment as usual (the two-day DBT for IPV skills group without the VIAs). The following hypotheses will be examined: 1) those in the experimental VIA condition will experience treatment gains above and beyond those in the control (treatment as usual) condition; 2) those in the experimental VIA condition will view the VIAs as acceptable; and 3) those in the experimental VIA condition will report a greater frequency of using the skills than those in the control condition.
Status | Completed |
Enrollment | 24 |
Est. completion date | July 1, 2019 |
Est. primary completion date | June 22, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Victim of domestic violence - Must be 18 years old or older - Speak English - Have a 8th grade reading level - Be a female - Have access to the internet Exclusion Criteria: - People who are suicidal |
Country | Name | City | State |
---|---|---|---|
United States | University of Nevada, Reno | Reno | Nevada |
Lead Sponsor | Collaborator |
---|---|
Rory Newlands |
United States,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in the difficulties in emotion regulation scale | The difficulties in emotion regulation scale is a 36 item self report questionnaire intended to assess multiple aspects of emotion dysregulation. Participants answer on a 1-5 likert scale, with higher scores indicating more problems with emotion regulation. Minimum score = 36 and maximum score = 180. There are six sub scales: Non-acceptance (minimum score = 6 maximum score = 36); difficulties engaging in goal directed behaviors (minimum score = 5 maximum score = 25); impulse control (minimum score = 6 maximum score = 36); lack of emotional awareness (minimum score = 6 maximum score = 36); limited access to emotion regulation strategies (minimum score = 8 maximum score= 40) and lack of emotional awareness (minimum score = 5 maximum score = 25). the sub scales are summed to create the total score. | pre-test (before beginning the intervention), 2 days post-test (after intervention completion), 1 month (after the completion of the intervention) and 3 month (after the completion of the intervention). The data will be uploaded at the end of the study | |
Secondary | Changes in the Acceptance and Action questionnaire II Questionnaire - II Acceptance and Action Questionnaire - II Acceptance and Action Questionnaire - II The acceptance and action questionnaire-II | The seven item questionnaire assesses psychological flexibility. Participants answer on a 1-7 likert scale, with higher scores indicating Higher scores indicating greater levels of psychological inflexibility. Minimum score = 7 and maximum score = 105. | pre-test (before beginning the intervention), 2 days post-test (after intervention completion), 1 month (after the completion of the intervention) and 3 month (after the completion of the intervention). The data will be uploaded at the end of the study | |
Secondary | Changes in the Brief symptom inventory | The brief symptom inventory is a 53 item self-report assessment designed to measure psychological distress as well as various psychological disorders/issues The BSI has nine subscales designed to assess individual symptom groups: somatization (SOM), obsessive-compulsive (OC), interpersonal sensitivity (IS), depression (DEP), anxiety (ANX), hostility (HOS), phobic anxiety (PHB, ), paranoid ideation (PAR), and psychoticism (PSY). The BSI also includes three scales that capture global psychological distress. Participants answer on a 0-4 likert scale, with higher scores indicating greater levels of psychopathology psychological issues. The minimum raw score is 0 and the maximum raw score is 212. Raw scores are converted to t-scores. The t-scores range from 30 to 80, with higher t-scores indicating greater disfunction. The global score equals the sum of all 53 items | pre-test (before beginning the intervention), 2 days post-test (after intervention completion), 1 month (after the completion of the intervention) and 3 month (after the completion of the intervention). The data will be uploaded at the end of the study | |
Secondary | Skills Use Follow-up questionnaire | This questionnaire asks participants if/how many times they have used the skills taught in the skills group since participating in the group. Responses range from 0 to 100, with higher numbers equating to higher usage of the skills. | pre-test (before beginning the intervention), 2 days post-test (after intervention completion), 1 month (after the completion of the intervention) and 3 month (after the completion of the intervention). The data will be uploaded at the end of the study | |
Secondary | Changes in the five facets of mindfulness questionnaire 15 item | This 15 item self-report question is designed to measure mindfulness. Participants answer on a 1-5 likert scale, with higher scores indicating greater levels of mindfulness. Minimum score = 15 and maximum score = 75. There are five sub scales: Observing (minimum score = 3 maximum score = 15); describing (minimum score = 3 maximum score = 15); acting with awareness (minimum score = 3 maximum score = 15); Non-judging (minimum score = 3 maximum score = 15); and non-reactivity (minimum score = 3 maximum score = 15). the sub scales are summed to create the total score. | pre-test (before beginning the intervention), 2 days post-test (after intervention completion), 1 month (after the completion of the intervention) and 3 month (after the completion of the intervention). The data will be uploaded at the end of the study | |
Secondary | Changes in the Post Traumatic Stress Disorder checklist for the DSM five civilian version | This 20 item self-report scale it is designed to capture symptoms of PTSD. Participants answer on a 0-4 likert scale, with higher scores indicating higher levels of PTSD symptomology. Minimum score = 0 and maximum score = 80. | pre-test (before beginning the intervention), 2 days post-test (after intervention completion), 1 month (after the completion of the intervention) and 3 month (after the completion of the intervention). The data will be uploaded at the end of the study |
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