Building Resilience In Caregivers of Trauma Survivors

Sponsor
The University of Texas Health Science Center, Houston (Other)
Overall Status
Recruiting
CT.gov ID
NCT04293016
Collaborator
United States Department of Defense (U.S. Fed)
300
1
3
17.9
16.8

Study Details

Study Description

Brief Summary

The purpose of the study is to examine the role of demographics, pre-existing anxiety, depression, and substance use on caregiver depression anxiety, and substance use following a critical injury to a loved one,evaluate the factors that mediate the effectiveness of traditional, psychotherapy using problem solving therapy to reduce depression, anxiety, and substance use and to evaluate the factors that mediate the effectiveness of providing an ICU diary and instruction on that diary to reduce depression, anxiety, and substance use.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Support as usual
  • Behavioral: problem solving therapy
  • Behavioral: ICU diary
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Building Resilience In Caregivers of Trauma Survivors
Actual Study Start Date :
Mar 1, 2022
Anticipated Primary Completion Date :
Aug 28, 2023
Anticipated Study Completion Date :
Aug 28, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Support as usual

Behavioral: Support as usual
this group receives current best practice which includes participation in ICU support groups and provision of community support resources

Experimental: Problem Solving therapy

Behavioral: problem solving therapy
This group will receive one on one therapy based on identifying stressors and solutions to those stressors

Experimental: ICU diary

Behavioral: ICU diary
This group will provided with a structured written diary that includes identification of stressors and development of solutions to those stressors

Outcome Measures

Primary Outcome Measures

  1. short form survey (SF-12) [6 months post injury]

    Quality of life of caregiver as assessed by the short form survey (SF-12).The SF-12 is a 12 item questionnaire with a range from 0 to 100, where a zero score indicates the lowest level of health measured by the scales and 100 indicates the highest level of health.

  2. Posttraumatic Stress Disorder Checklist(PCL-5) [6 months post injury]

    The extent to which caregivers have been bothered by PTSD symptoms as assessed by the PTSD Checklist (PCL-5) assessment.The PCL-5 evaluates how much participants have been bothered by PTSD symptoms in the past week (for all assessments during treatment) or the past month (all other assessment time points) as a result of a specific life event. Each item of the PCL-5 is scored on a five-point scale ranging from 0 "not at all") to 4 ("extremely).

  3. The Hamilton Depression Rating Scale (HAM-D) [6 months post injury]

    Symptoms of depression in caregivers as assessed by the The Hamilton Depression Rating Scale (HAM-D).Although the HAM-D form lists 21 items, the scoring is based on the first 17. Eight items are scored on a 5-point scale, ranging from 0 = not present to 4 = severe. Nine are scored from 0(Absent)-2(frequent)

Secondary Outcome Measures

  1. The center for epidemiologic studies of depression (CESD-R ) [3 months post injury]

    Depression in caregivers as assessed by the CESD-R tool The CESD-R scale has 20 items and each is measured from 0(not at all) to 4(nearly every day for 2 weeks)

  2. PTSD Checklist for (PCL-5) assessment. [3 months post injury]

    The extent to which caregivers have been bothered by PTSD symptoms as assessed by the PTSD Checklist (PCL-5) assessment.The PCL-5 evaluates how much participants have been bothered by PTSD symptoms in the past week (for all assessments during treatment) or the past month (all other assessment time points) as a result of a specific life event. Each item of the PCL-5 is scored on a five-point scale ranging from 0 "not at all") to 4 ("extremely).

  3. The Alcohol Use Disorders identification Test (AUDIT): [3 months post injury]

    Alcohol use problems in caregivers as assessed by the AUDIT scale This is a 10-item screening tool and is rated between 0-4-the higher number indicating a worse outcome

  4. Number of days of hospitalization [6 months post injury]

    medical record based review of hospital readmission

  5. Number of infections post discharge [6 months post injury]

    medical record based review of number of infections after discharge

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Must anticipate serving in a Caregiver role after the patient is discharged (A. Must be either a family member or close friend of a patient who has been admitted to the trauma/critical care service ICU B. Must anticipate spending time with the patient in a caregiver or other supportive role (e.g.,emotional, social, financial) after the patient is discharged)

  • Caregiver and patient must report English as a primary language

  • patient and Caregiver must be able to provide informed consent

  • Caregiver must be able to provide at least two forms of contact information

  • Trauma Patient directly admitted to the ICU (Primary cause of admission is trauma, Injury must include trauma to the head/brain, Admitted directly to the hospital ,Patient admission of at least 48 hours , Patient is currently admitted to the ICU ,Patient is expected to survive more than 96 hours at 48 hours after admission,Patient has an abbreviated injury score greater than 3 (severe, critical, maximum) ,Fluent in English)

  • Trauma patient must be able t communicate verbally

Exclusion

  • Does not anticipate serving in a Caregiver role after the patient is discharged

  • Caregiver is not a close friend or family member of the patient who has been admitted to the ICU

  • Caregiver does not expect to serve in a supportive role to the patient

  • caregiver does not meet inclusion criteria as stated above

  • Patient is not currently admitted to the ICU and or is not expected to remain in the ICU for 48 hours

  • Patient is not expected to survive more than 96 hours

  • Patient is not expected to require assistance prior to discharge

  • Patient is not between 18 and 65 years of age

Contacts and Locations

Locations

Site City State Country Postal Code
1 The University of Texas Health Science Center at Houston Houston Texas United States 77030

Sponsors and Collaborators

  • The University of Texas Health Science Center, Houston
  • United States Department of Defense

Investigators

  • Principal Investigator: Deborah M Little, PhD, The University of Texas Health Science Center, Houston

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Deborah M Little, Professor, The University of Texas Health Science Center, Houston
ClinicalTrials.gov Identifier:
NCT04293016
Other Study ID Numbers:
  • HSC-MS-19-0073
First Posted:
Mar 3, 2020
Last Update Posted:
Apr 19, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Deborah M Little, Professor, The University of Texas Health Science Center, Houston
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 19, 2022