Trauma and Stressor Related Disorders, Violence, Domestic, Violence, Sexual, Violence, Structural
Conditions
Keywords
trauma, violence, abuse
Brief summary
The goal of this prospective study is to test the: acceptability of trauma-informed care plans; the intervention appropriateness; and the feasibility of the trauma-informed care plans in the electronic health care record. Patient seen in various health care settings and how have complex health care needs will be invited to participate in this study. The aims to are: Aim 1: Explore the acceptability of trauma-informed care plans, the appropriateness of trauma-informed care plans, and the feasibility of Trauma-Informed Care Plans(TICP) when used by clinicians on the health care team (HCTC). Hypothesis 1: HCTC using the TICP will report its acceptability, feasibility, satisfaction and ease of use. Hypothesis 2: HCTC will report heightened awareness of intersection of trauma and social determinants of health. Hypothesis 3: HCTC will report more awareness of the patient's unique preferences and will be better informed regarding the unique plan of care for their patient. Aim 2: Explore the impact of having a TICP by patients understanding how the TICP may have improved their experience around care and treatment. Hypothesis 1: patients will report: improved satisfaction with their care. Hypothesis 2: patients will report feeling better known by HCT. Hypothesis 3: will report less stress and anxiety related to health care encounters.
Interventions
OTHERTrauma-informed Care Plan-
Per our IRB protocol patient participates will be consented for this study. A member of the healthcare team ( licensed nurse, social worker or doctor) will conduct the TICP with the patient. The TICP will be placed in the electronic medical record right below the patients name. The workflow is such is that if any plan of care placed on the Storyboard (under the patient's name) should be read first before engaging with a patient.
Sponsors
Brigham and Women's Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Masking description
Participants (patients and providers) will be de-identified
Intervention model description
This is a prospective study designed to explore the acceptability, intervention appropriateness of trauma-informed care plans and the feasibility of trauma-informed care plans by patients and members of the health care team
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
* patients ( ages 18-60) * who have frequent health care appointments * have complex health care needs * consent to participate in study * English or spanish speaking.
Exclusion criteria
* patients less than 18 and older than 60. * patients too ill (medically/phytologically) to consent. * suicidal or homicidal patients.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Acceptability of Trauma Informed Care Plans | 6-10 months | This study is exploring the acceptability of trauma-informed care plans by the percentage of patients and clinicians that find the TICP acceptable |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Intervention Appropriateness of Trauma-Informed Care plans | 6-10 months | This study is exploring the appropriateness of trauma-informed care plans by the percentage of patients and clinicians that find the TICP to be appropriate |
| Feasibility of the trauma-informed care plans | 6- 10 months | This study is exploring the feasibility of the trauma-informed care plans by the percentage of patients and clinicians that find the trauma-informed care plans to be feasible. |
Countries
United States
Outcome results
None listed