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NCT03108820 · ClinicalTrials.gov registry record · NA

Trauma Medical Home for Older Injured Patients

A NA study, sponsored by Indiana University.

Completed
Registry status
NA
Development phase
430
Enrollment target

NCT03108820: Completed NA study, sponsored by Indiana University.

NCT03108820 is a NA study that has completed, run by Indiana University. The registered enrollment target is 430 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (69% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03108820, a NA study, has completed, sponsored by Indiana University.

COMPLETED
Registry status
NA
Development phase
430 participants
Enrollment target

Study 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.

Primary Outcome

As determined using the Physical Component Score of Short form (SF) SF-36. Score range: 0-100, higher scores indicate a better health state. The change is between baseline and 12 months.

Interventions

  • OTHER Usual Care
  • BEHAVIORAL TMH Intervention

Trial Details

FieldValue
Enrollment Target 430 participants
Start Date 2017-10-01
Est. Completion 2023-03-01
Phase NA
Indiana University

890 total trials

What the finished NCT03108820 record still lists

NCT03108820 is an interventional study that assigns participants to a tested intervention. The registered 430 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (69% lower).

The record links to 0 conditions, and to 2 interventions - of which Usual Care is the first listed.

NCT03108820 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03108820 about?

NCT03108820 is a clinical study titled "Trauma Medical Home for Older Injured Patients". 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...

What is the current status of trial NCT03108820?

This trial is currently completed. It is a NA study. The enrollment target is 430 participants. The study started on 2017-10-01. Estimated completion is 2023-03-01.

What interventions are being tested in trial NCT03108820?

The interventions under investigation include: Usual Care (OTHER), TMH Intervention (BEHAVIORAL).

Who is sponsoring clinical trial NCT03108820?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03108820's enrollment target sits among peer trials

430 235th of 2000 higher than 1,765 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03108820, the US trial registry maintained by the National Library of Medicine. NCT03108820 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.