NCT02041585

Brief Summary

The DC PROMIS Study (also known as the Discharge Patient Reported Outcomes Measurement Information System Study) is a study to see the effect of patients' social, physical and mental function on their health after hospital discharge.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2012

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2012

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

January 15, 2014

Completed
7 days until next milestone

First Posted

Study publicly available on registry

January 22, 2014

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2014

Completed
Last Updated

March 6, 2023

Status Verified

March 1, 2023

Enrollment Period

1.5 years

First QC Date

January 15, 2014

Last Update Submit

March 2, 2023

Conditions

Keywords

Hospital ReadmissionSocial Isolation and Hospital ReadmissionAge and Hospital ReadmissionFunctional Status and Hospital ReadmissionCharlson Score and Hospital ReadmissionLength of Stay and Hospital Readmission

Outcome Measures

Primary Outcomes (1)

  • 30 day rehospitalization

    Rehospitalization is an important clinical quality/healthcare utilization measure. In this study it will be measured using patient report of rehospitalization collected via telephone followup.

    Measured at 30 days following hospital discharge

Study Arms (1)

Elder discharge cohort

There will be no intervention in this observational survey research.

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

General medical service inpatient hospitalist service population, aged greater than or equal to 65

You may qualify if:

  • patients cared for on the inpatient general medical and surgical services at Northwestern Memorial Hospital (NMH)
  • age upon admission ≥65 years
  • anticipated disposition to home at discharge or within two weeks of discharge

You may not qualify if:

  • previous hospitalization within 30 days
  • in-hospital death
  • transfer to another inpatient facility at the time of discharge
  • non-English language fluency
  • hospital medicine attending attestation that patient is not competent or clinically stable to participate
  • Mini-cog evaluation consistent with dementia

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Northwestern Memorial Hospital

Chicago, Illinois, 60611, United States

Location

MeSH Terms

Conditions

Social IsolationDepressionAnxiety DisordersFrailty

Condition Hierarchy (Ancestors)

Social BehaviorBehaviorBehavioral SymptomsMental DisordersPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Luke Hansen, MD, MHS

    Northwestern Memorial Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
30 Days
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

January 15, 2014

First Posted

January 22, 2014

Study Start

October 1, 2012

Primary Completion

April 1, 2014

Study Completion

April 1, 2014

Last Updated

March 6, 2023

Record last verified: 2023-03

Locations