Trauma Medical Home for Older Injured Patients

NCT03108820 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 430

Last updated 2024-06-24

Study results available
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Summary

This proposal aims to conduct a randomized controlled trial to evaluate the efficacy of a 6-month collaborative care intervention in improving the functional and psychological recovery of 430 injury survivors 50 and older. The trial has the following specific aims: 1) Evaluate the ability of the TMH intervention to improve the physical recovery of older injury survivors; and 2) Evaluate the ability of the TMH intervention to improve the psychological recovery of older injury survivors; and 3) Evaluate the ability of the TMH intervention to reduce healthcare costs of older injury survivors and evaluate the cost of effectiveness of the TMH intervention.

Conditions

  • Injuries

Interventions

BEHAVIORAL

TMH Intervention

Home visits and close interaction with injured patient to assure plan for care is being followed.

OTHER

Usual Care

Review hospital discharge and rehabilitation plan, identification of primary care provider, provision of educational materials on communication skills, caregiver coping skills, and legal and financial advice.

Sponsors & Collaborators

  • National Institutes of Health (NIH)

    collaborator NIH
  • Northwestern University

    collaborator OTHER
  • University of Missouri, Kansas City

    collaborator OTHER
  • National Institute on Aging (NIA)

    collaborator NIH
  • Indiana University

    lead OTHER

Principal Investigators

  • Ben Zarzaur, MD, MPH · University of Wisconsin, Madison

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-01
Primary Completion
2023-03-01
Completion
2023-03-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03108820 on ClinicalTrials.gov