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N/A N=187

Screening and Interventions in an Acute Care Setting

Depression · Medication Administered in Error · Cognitive Impairment

Enrolled (actual)
187
Serious AEs
0.0%
Results posted
Sep 2012
Primary outcome: Primary: Proportion of Subjects Cognitively Impaired in Emergency Medical Services (EMS) — 17 percentage of subjects

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Older Adult · 65+ yrs
Sex
All
Sponsor
University of Rochester
Primary completion
Jun 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Proportion of Subjects Cognitively Impaired in Emergency Medical Services (EMS)
17
PRIMARY
Proportion of Subjects Cognitively Impaired in the Emergency Department (ED)
16
PRIMARY
Proportion of Subjects Cognitively Impaired in the ED
55
PRIMARY
Test-Retest Reliability of Six Item Screener Screening
0.52
PRIMARY
Concurrent Criterion Validity of Six Item Screener Screening
0.23
PRIMARY
Proportion of Subjects Depressed in EMS.
48
PRIMARY
Proportion of Subjects Depressed in the ED
22
PRIMARY
Proportion of Subjects Depressed in the ED
22
PRIMARY
Test-Retest Reliability Testing of PHQ-2 Screening
0.50
PRIMARY
Concurrent Criterion Validity of PHQ-2
0.36

Summary

The purpose of this study is to: 1) evaluate the reliability and validity of EMS screening for depression and cognitive impairment and 2) to develop a pilot ED intervention program to address the needs of older adults found to be at risk for depression and cognitive impairment.

Eligibility Criteria

Inclusion Criteria

  • age 65 or older, cared for by participating EMS providers

Exclusion Criteria

  • too ill to participate, not transported to participating hospitals
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00545155). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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