Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UC Davis UCSF
Dates
study started
completion around

Description

Summary

The goal of this observational study is to validate a novel patient-reported outcome measure (PROM) for patients suffering maxillofacial trauma: The Survey for Maxillofacial Trauma and Soft Tissue Healing (SMASH-Q). The primary question is:

Are the SMASH-Q modules valid and reliable measures to study quality-of-life (QOL) in patients with maxillofacial trauma?

Patients presenting for routine clinic follow-up for maxillofacial trauma will be invited to complete the SMASH-Q in addition to the 15 Dimension (15D) QOL survey as a control.

Official Title

Multi-Institutional Validation of the Survey for Maxillofacial Trauma and Soft Tissue Healing (SMASH-Q)

Details

Background: Maxillofacial trauma literature is dominated by objective and physician-rated outcomes, leaving a paucity of patient-reported outcome (PRO) research. In fact, no PRO measure (PROM) has ever been validated in this population, posing a tremendous barrier to our understanding of the patient experience. This project will overcome this barrier by validating a novel PROM designed by our research group: The Survey for Maxillofacial Trauma and Soft Tissue Healing (SMASH-Q). The SMASH-Q is the first PROM designed for maxillofacial trauma, providing novel insight into the patient experience. In its current form, it is a 4-module survey instrument: one general module for all patients (SMASH) and 3 modules specific to fractures of the nasal (N-SMASH), orbital (O-SMASH), and/or jaw (J-SMASH) regions. Each module takes 2-5 minutes to complete for a total of 2-20 minutes, depending on the injury.

Objectives: This study will be a multi-institutional field test to determine the validity and reliability of using the SMASH-Q for measuring QOL in patients suffering maxillofacial trauma. The hypothesis is that each SMASH-Q module and subscale will significantly and at least moderately correlate with the 15D, an established general QOL survey instrument.

Methods: Patients with maxillofacial trauma presenting for routine follow-up within one year from their injury will be invited to complete the SMASH-Q and the 15D survey. Patients who completed an initial survey and return within one month will be invited to complete a second follow-up survey. The scores be tested for validity and reliability using multivariable linear regression, Pearson's r, Cronbach alpha, and test-retest reliability. The minimally clinically important difference (MCID) will also be calculated.

impact: Validation of the first PROM for maxillofacial trauma is anticipated to have a significant and lasting impact in the field of maxillofacial trauma. This will allow researchers and clinicians to better understand the patient experience and make management recommendations accordingly. Integrating the SMASH-Q into future studies may revolutionize the field by providing novel evidence for controversial topics such as maxillomandibular fixation techniques, surgical approaches, adjunctive therapies, and more.

Keywords

Facial Injuries, Mandible Fracture, Le Fort, Zygomaticomaxillary Complex Fracture, Nasal Fracture, Orbital Fractures, Zygoma Fracture, Orbital Floor Fracture, Facial Laceration, Facial Trauma, Maxillofacial Trauma, Patient-Reported Outcomes, Quality of Life, SMASH, Midface Fracture, Orbital Fracture, Mandibular Fractures, Facies, Bone Fractures, Lacerations, SMASH Module, N-SMASH Module, O-SMASH Module, J-SMASH Module, Nasal Fractures (N-SMASH), Orbital Fractures (O-SMASH), Jaw Fractures (J-SMASH)

Eligibility

You can join if…

Open to people ages 18 years and up

  1. Diagnosis of maxillofacial trauma (fracture of any facial bone[s] and/or soft tissue injury) within 12 months of recruitment date.

You CAN'T join if...

  1. Patients presenting to clinic for reasons not related to maxillofacial trauma.
  2. Patients with isolated fractures of the cranium or teeth.
  3. Patients who cannot read, write, and/or speak English.
  4. Patients who are unable to provide informed consent for themselves (including those who are under 18 years old, incapacitated, intoxicated, or cognitively impaired with a legal guardian)

Locations

  • University of California, Davis
    Sacramento California 95817 United States
  • University of California, San Francisco
    San Francisco California 94110 United States
  • University of Tennessee Health Science Center
    Memphis Tennessee 38103 United States

Details

Status
accepting new patients by invitation only
Start Date
Completion Date
(estimated)
Sponsor
University of Tennessee
ID
NCT06850857
Study Type
Observational
Participants
Expecting 500 study participants
Last Updated