SWIFT Study in the ED (SWIFT)

April 25, 2016 updated by: Megan Moore, University of Washington

Social Work Intervention for Adults With Mild Traumatic Brain Injury: SWIFT Pilot Study

Mild traumatic brain injury (mTBI) is a prevalent and costly public health problem with disabling consequences. More than one million civilians with mTBI are treated in US hospitals and emergency departments each year (Faul, et al., 2010). While the exact number is debated, approximately 10-15% of individuals with mTBI will experience prolonged and disabling post-concussive symptoms (Stranjalis, et al., 2008; Ruff and Weyer Jamora, 2009), and 34% will experience a psychiatric illness in the first year after injury (Fann, et al., 2004). In addition, at least 188,270 military service members sustained a TBI from 2000 to mid August 2010, and nearly 77% of these injuries were mild (Defense and Veterans Brain Injury Center, 2010). Many individuals require treatment for resulting mTBI symptoms.

The proposed study builds on preliminary research conducted by the investigators to develop and test the effectiveness of a social work delivered education and reassurance intervention for adults with mTBI (SWIFT-Acute) against usual care. The proposed study will assess acceptability and obtain preliminary effectiveness data for an enhanced social work assessment and intervention for adults with mTBI (SWIFT) discharged from the Emergency Department (ED). SWIFT includes early education, reassurance, coping strategies, resources and a brief alcohol use intervention in the ED plus follow up telephone counseling, needs assessment and case management referral to necessary services. The intervention targets cognitive, physical, psychiatric and functional outcomes; specifically, post-concussive symptoms, depression, anxiety, posttraumatic stress disorder, alcohol use, community functioning and successful linkage to community resources.

It is hypothesized that SWIFT will be acceptable to patients and that participants in the SWIFT group will report superior outcomes on measures of post-concussive symptoms, depression and anxiety, alcohol use and community functioning and will report increased successful linkages to needed resources when compared to the SWIFT-Acute group.

The specific aims of the study are:

  1. Implement an innovative social work intervention for adults with mTBI (SWIFT).
  2. Assess acceptability of SWIFT using qualitative interviews with participants.
  3. Assess preliminary effectiveness of SWIFT compared to SWIFT-Acute alone on reduction or prevention of post-concussive symptoms, depression, anxiety, posttraumatic stress disorder (PTSD) symptoms, and alcohol use, and on improvement of community functioning and successful linkage to community resources. 80 participants will be randomized to receive SWIFT or SWIFT-Acute. Preliminary intervention effectiveness will be assessed using standard measures of post-concussive symptoms, the primary outcome, depression, anxiety, PTSD, alcohol use, and community functioning. A structured survey will be used to assess linkage to community resources.

Study Overview

Status

Unknown

Study Type

Interventional

Enrollment (Anticipated)

80

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • California
      • San Francisco, California, United States, 94110
        • Recruiting
        • UCSF San Francisco General Hospital and Trauma Center
        • Contact:
        • Principal Investigator:
          • Geoffrey Manley, MD, PhD
        • Sub-Investigator:
          • Martha Shumway, PhD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

Inclusion criteria are based on the World Health Organization definition of mTBI. For inclusion in the study, participants must meet following criteria:

  1. At least 18 years of age and English speakers
  2. Present to ED with mechanism of trauma to the head, non-penetrating injury, or recent history of trauma to the head
  3. Glasgow Coma Scale score of 13-15 after 30 minutes post injury or later upon presentation for healthcare
  4. Discharged from the ED in <48 hours from time of admission
  5. In addition participants must have one or more of the following symptoms at time of injury:

    1. confusion or disorientation
    2. loss of consciousness for 30 minutes or less,
    3. post-traumatic amnesia for less than 24 hours
    4. other transient neurological abnormalities such as focal signs, seizure and intracranial lesion not requiring surgery

Exclusion Criteria:

  1. the manifestations of mTBI are determined to be caused by penetrating craniocerebral injury
  2. patients <18 years of age or non-English speaking
  3. patients with intracranial lesion requiring surgery
  4. patients admitted to the hospital from ED
  5. patients in police custody
  6. patients without a telephone contact number

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: SWIFT: Acute Social Work Intervention in the ED and Follow Up
Participants will receive: 1) acute social work intervention for adults with mTBI, including early education, reassurance, resources and brief alcohol intervention in the ED (SWIFT-Acute) and 2) follow up telephone counseling, needs assessment and case management referral to necessary services (SWIFT).
Participants will receive: 1) acute social work intervention for adults with mTBI, including early education, reassurance, resources and brief alcohol intervention in the ED (SWIFT-Acute) and 2) follow up telephone counseling, needs assessment and case management referral to necessary services (SWIFT).
Active Comparator: SWIFT-Acute Only: Acute social work intervention in the ED
acute social work intervention for adults with mTBI, including early education, reassurance, resources and brief alcohol intervention in the ED (SWIFT-Acute)
acute social work intervention for adults with mTBI, including early education, reassurance, resources and brief alcohol intervention in the ED (SWIFT-Acute)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Change in Rivermead Postconcussion Symptoms Questionnaire (RPQ)
Time Frame: baseline, 3mo, 6mo
baseline, 3mo, 6mo

Secondary Outcome Measures

Outcome Measure
Time Frame
Change in Headache Impact Test (HIT-6)
Time Frame: baseline, 3mo, 6mo
baseline, 3mo, 6mo
Change in Insomnia Severity Index (ISI)
Time Frame: baseline, 3mo, 6mo
baseline, 3mo, 6mo
Change in The Post Traumatic Stress Disorder Checklist (PCL-C)
Time Frame: baseline, 3mo, 6mo
baseline, 3mo, 6mo
Change in Cornell Service Index
Time Frame: baseline, 3mo, 6mo
baseline, 3mo, 6mo
Change in The Alcohol Use Disorders Identification Test (AUDIT)
Time Frame: baseline, 3mo, 6mo
baseline, 3mo, 6mo
Change in Community Integration Questionnaire (CIQ)
Time Frame: baseline, 3mo, 6mo
baseline, 3mo, 6mo
Change in Patient Health Questionnaire (PHQ)-9
Time Frame: baseline, 3mo, 6mo
baseline, 3mo, 6mo
Change in Generalized Anxiety Disorder (GAD)-7
Time Frame: baseline, 3mo, 6mo
baseline, 3mo, 6mo

Other Outcome Measures

Outcome Measure
Time Frame
Standardized Assessment of Personality: Abbreviated Scale (SAPAS)
Time Frame: baseline
baseline
Change in Short Orientation Memory Concentration Test
Time Frame: baseline, 3mo, 6mo
baseline, 3mo, 6mo

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Megan Moore, MSW, PHD, University of Washington

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2013

Primary Completion (Anticipated)

July 1, 2016

Study Completion (Anticipated)

September 1, 2016

Study Registration Dates

First Submitted

June 28, 2013

First Submitted That Met QC Criteria

July 8, 2013

First Posted (Estimate)

July 9, 2013

Study Record Updates

Last Update Posted (Estimate)

April 27, 2016

Last Update Submitted That Met QC Criteria

April 25, 2016

Last Verified

April 1, 2016

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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