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Synergy Between Patient and Clinician: Using a Trauma-Informed Care Plan (TICP)

Mass General Brigham logo

Mass General Brigham

Status

Invitation-only

Conditions

Violence, Structural
Violence, Sexual
Trauma and Stressor Related Disorders
Violence, Domestic

Treatments

Other: Trauma-informed Care Plan-

Study type

Interventional

Funder types

Other

Identifiers

NCT06330753
2024P000682

Details and patient eligibility

About

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.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

200 participants in 1 patient group

Feasibility and Acceptability of Trauma-informed Care Plans (TICP)
Other group
Description:
Per our IRB protocol - Patient participants and clinician participants will be asked (via a survey) to rate their: Acceptability of the Trauma-informed Care Plan, the Appropriateness of the TICP and the feasibility of the TICP. The intervention is the TICP place in the Electronic Medical Record right below the patient's name (on the Storyboard).
Treatment:
Other: Trauma-informed Care Plan-

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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