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Completed

NCT Number: NCT02063087

Shared Decision Making in Parents of Children With Head Trauma: Head CT Choice

The investigators will test the impact of a decision aid, Head CT Choice, to determine if its use improves parents' knowledge and engagement in decision making and safely decreases healthcare utilization in children presenting to the emergency department with blunt head trauma.

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Key information

Age range

Up to 18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of California, Davis Medical Center, Sacramento, California, United States

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About this study

The investigators' long term goal is to promote evidence-based, patient-centered evaluation in the acute setting, to more closely tailor testing to disease risk. The investigators will compare the use of risk stratification tools with usual clinical approaches to treatment selection or administration through the following aim:

Test if the decision aid, Head CT Choice, improves validated patient-centered outcome measures and safely decreases healthcare utilization. The investigators will randomize at the clinician level. Through the use of the intervention, Head CT Choice, the investigators aim to significantly increase parents' knowledge, engagement, and satisfaction, decrease the rate of head CT use, and decrease 7-day total healthcare utilization, with no significant increase in adverse events.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Parents and their child, seeking care for a child who:

  • Is < 18 years of age;
  • Had blunt trauma above the eyebrows (not isolated to face or eyes);
  • Is positive for at least 1 of the PECARN clinical prediction rule predictors described below:

PECARN Predictors for children < 2 years of age:

Severe mechanism (PECARN definition)* Loss of consciousness > 5 seconds Acting abnormally per parent Initial ED GCS < 15 by attending (or CT decision-maker) Other signs of altered mental status (PECARN definition) Presence of occipital, temporal or parietal scalp hematoma Palpable skull fracture or unclear if skull fracture

PECARN predictors for children 2-18 years of age:

Severe mechanism (PECARN definition)* Any loss of consciousness Any vomiting since the injury Severe headache in ED Initial ED GCS < 15 by attending (or CT decision-maker) Other signs of altered mental status (PECARN definition)** Any sign of basilar skull fracture Clinicians include attending physicians and fellows or midlevel providers caring for children with head trauma

Exclusion criteria

Parents of children with:

  • GCS scores < 15
  • Evidence of penetrating trauma, signs of basilar skull fracture, or depressed skull fracture on physical examination
  • Brain tumors
  • Ventricular shunts
  • Bleeding disorder
  • Pre-existing neurological disorders complicating assessment
  • Neuroimaging at an outside hospital before transfer
  • Signs of altered mental status (agitation, somnolence, repetitive questioning, or slow response to verbal communication)
  • Syncope or seizure disorder preceded (led to) head trauma or seizure post head trauma
  • Known to be pregnant
  • Communication barriers such as visual or hearing impairment that may preclude use of the decision aid.
  • Strong suspicion of abuse for this head injury

Treatment and study plan

Head CT Decision Aid

Other

The decision aid, Head CT Choice, educates parents regarding how the clinician determined the severity of their child's head trauma, their child's quantitative risk for a clinically-important TBI, the pros and cons of cranial CT compared to active observation, and what signs and symptoms parents should watch for in the next 24 hours that should prompt a return visit to the ED.

Primary outcomes

  1. Assess Parents' Knowledge Regarding Their Child's Risk for a Significant Brain Injury

    Time frame: Day 1 (immediately after the clinical encounter)

    Knowledge will be measured by means of a post visit survey delivered immediately after the clinical encounter in the emergency department. The investigators will assess parents' knowledge regarding their child's quantitative risk for a significant brain injury, the pros and cons of head CT compared to active observation, and what signs and symptoms parents should watch for in the next 24-48 hours that should prompt a return visit to the ED. Each knowledge question will provide the parent(s) with three options to respond (True, False, or Unsure), and the parent(s) will receive a score of 1 for a correct response and 0 for an incorrect response and any response of 'Unsure' will be considered incorrect. An overall score will be calculated by summing the correct responses and dividing by the number of questions asked.

Secondary outcomes

  1. Patient Engagement in the Decision-making Process

    Time frame: Day 1 (during the ED visit)

    Using the OPTION validated scale, the investigators will measure the degree to which clinicians engage parents' in the decision making process. The OPTION scale will be assessed by having 2 observers independently review and score the video recordings of the encounter between the parent and the child's emergency department clinician. The OPTION scale is composed of 12 items with a value of 0-4; they are summed, divided by 48 and multiplied by 100. This creates a score that ranges from 0-100, where higher scores are reflective of a higher level of parental engagement.

  2. Decisional Conflict

    Time frame: Day 1 (immediately after the clinical encounter)

    The investigators will measure the degree of conflict patients experience related to feeling uninformed using the validated Decisional Conflict Scale (DCS). The 16 items of DCS are scored on a 0-4 scale; the items are summed, divided by 16 and then multiplied by 25. The scale is from 0-100 where higher scores are reflective of parental uncertainty about the choice.

  3. Trust in the Physician

    Time frame: Day 1 (immediately after the clinical encounter)

    The investigators will measure parents' trust in their clinician using the validated Trust in Physician Scale (TPS). There are 9 items with a scale of 1-5, the items are subtracted by 1, summed, divided by 9 and then multiplied by 25. The scale ranges from 0-100 where higher values are reflective of higher levels of trust in their physician.

  4. Parental Satisfaction

    Time frame: Day 1 (immediately after the clinical encounter)

    The investigators will assess parents' satisfaction by comparing the number of patients who reported being "strongly satisfied" with their choice.

  5. Proportion of Children Who Undergo Head CT

    Time frame: Day 1 (anytime during the index emergency department visit)

    The study coordinator will ascertain whether the child underwent head CT in real time and confirm the data by health record review.

  6. Healthcare Utilization - Number of Tests Ordered Within 7 Days

    Time frame: 7-days

    The investigators will assess healthcare utilization for the subsequent 7-days after the ED visit. Healthcare utilization will include measures such as hospitalization, re-hospitalization, primary and specialty visits, and diagnostics including CT use which will be obtained via a health record review, review of itemized hospital charges on the UB-92 and UB-04 forms (summary billing statements), and parental report via the 7 day follow-up by the study coordinator. Outcomes are reported as number of tests or procedures per patient, categorized based on the Berenson-Eggers Types of Service (BETOS) codes.

  7. Rate of Clinically Important Traumatic Brain Injury (ciTBI)

    Time frame: 7-days

    The investigators will assess safety by comparing the rate of ciTBI in each arm of the study. The investigators will define ciTBI as we did in the original PECARN study: death from TBI, intubation for more than 24 hours for TBI, neurosurgical procedure, or hospital admission of 2 nights or more associated with TBI on CT.

  8. Fidelity - Options for Care

    Time frame: Day 1

    We will measure the degree to which the intervention is implemented as intended in both intervention and control groups when reviewing the recordings. The recordings in the intervention group will serve as a measure of the fidelity with which the intervention was delivered as intended. We will use a checklist of elements present and absent for quantification of implementation.

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Collaborators

  • Boston Children's Hospital
  • Children's Hospitals and Clinics of Minnesota
  • Columbia University
  • Flying Buttress Associates
  • Nationwide Children's Hospital
  • Patient-Centered Outcomes Research Institute
  • University of California, Davis
  • University of Minnesota Masonic Children's Hospital

Registry information

Important dates

Study start
2014
Primary completion
2016
Study completion
2017
First posted
Feb 14, 2014
Registry last updated
May 9, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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