Discharge Functional Status and Rehospitalization in the Elderly

Depression Clinical Trial

— DC PROMIS  

Official title:

The Contribution of Low Physical Function, Emotional Function and Social Support to Rehospitalization Risk Among Older Adults

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02041585
• Other study ID #: DCPROMIS
• Status: Completed
• Start date: October 2012
• Est. completion date: April 2014

Study information

• Verified date: March 2023
• Source: Northwestern University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial 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.

Description:

Background: Rehospitalization within 30 days of discharge is observed in approximately 19% of Medicare Fee for Service patients following discharge. Risk factors including medical comorbidity and discharge process quality have been identified as contributing to this outcome, however the possibility that patient level social and functional characteristics has not been equally investigated. Procedural summary: Patients will be recruited at the time of discharge. Participation in the study will include three surveys (one at the time of discharge, one within 72-96 hours after discharge and one thirty days after discharge) about functional status. The survey will inquire about function in six domains: physical function, depression, anxiety, cognition, social isolation, instrumental social support. The initial survey will be conducted in person at the hospital bedside by a research team member. The second and third surveys will be conducted by telephone within 72 to 96 day hours of discharge. Survey responses will be collected by direct patient response into tablet computer hardware. Recruitment: The research team (PI or RA) will identify candidates for recruitment based on conversation with the hospital case management staff and hospitalist physicians at the time of daily interdisciplinary care rounds. Inclusion criteria are age greater than or equal to 65 and anticipated return to home-based care at discharge or within two weeks of discharge. Exclusion criteria are non-English speaking language status, inability to complete interview based on sensory limitations, Mini-Cog evaluation consistent with dementia, or physician caregiver recommendation that patient not be enrolled. Risk: Participation in this study will not involve any physical risk beyond that of every day life. Risk will be minimized as no invasive interventions will be used. The possibility of psychological stress exists as individuals participate in interviews and complete survey items designed to test performance. Subjects may feel embarrassed to report areas of functional limitation. Risk of emotional harm will be minimized through the supportive presence of the PI and/or RA at the time of data collection and the use of geriatric appropriate strategies for interviewing. The patient will only be approached with hospital physician recommendation. Data Safety Primary data will be de-identified and carefully maintained in a locked area.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 300
• Est. completion date: April 2014
• Est. primary completion date: April 2014
• Accepts healthy volunteers: No
• Gender: All
• Age group: 65 Years and older

Eligibility

Inclusion Criteria:

• 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

Exclusion Criteria:

• 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

Related Conditions & MeSH terms

• Anxiety
• Debility
• Depression
• Frailty
• Social Isolation

Locations

Country	Name	City	State
United States	Northwestern Memorial Hospital	Chicago	Illinois

Sponsors (1)

Lead Sponsor	Collaborator
Northwestern University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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