- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02942524
Checklist Tool in Engaging Patients in the Discharge Planning Process (TEPID)
Tool to Engage Patients in Discharge (TEPID)
Study Overview
Status
Intervention / Treatment
Detailed Description
PRIMARY OBJECTIVES:
I. Measure the impact on discharge and transition satisfaction of utilizing questions from the Consumer Assessment of Healthcare Providers and Systems (CHAPS) patient satisfaction survey.
II. Measure the impact of the Tool to Engage Patients in Discharge (TEPID) on patient's Readiness for Hospital Discharge and Problems After Discharge Questionnaire-English (PADQ-E) results.
III. Measure the impact on decreasing healthcare utilization measures: readmission rates within 30 days from hospital discharge, hospital length of stay of admission in hospital, and emergency department visits within 30 days of hospital discharge.
OUTLINE:
Patients complete the TEPID checklist of items during hospital stay.
After completion of the study, patients are followed up for 35 days.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ohio
-
Columbus, Ohio, United States, 43210
- Ohio State University Comprehensive Cancer Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients fluent in English, conscious, coherent, and alert or have an adult caregiver present that is fluent in English will be identified for the TEPID research project
Exclusion Criteria:
- Patients discharged to another inpatient facility (hospice, skilled nursing facility, long term acute care hospital [LTACH], or acute rehab) or patients discharged home with hospice will be excluded
- Any patients that are transferred to another unit prior to discharge will be excluded
Study Plan
How is the study designed?
Design Details
- Primary Purpose: SUPPORTIVE_CARE
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Supportive care (TEPID)
Patients complete the TEPID checklist of items during hospital stay.
|
Ancillary studies
Ancillary studies
Complete TEPID
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Average score from the PADQ-E
Time Frame: Up to 12 months
|
A simple analysis of variance (ANOVA) model with floor as a fixed blocking factor treatment (TEPID or no TEPID) as a fixed factor.
Unit appears in the model as a nested factor within treatment, and statistical tests will be adjusted for this nesting structure.
The main test of interest in each model is the overall effect of treatment, which quantifies the effect of TEPID on the average score for the response.
P-values below 0.05 for this effect will be considered statistically significant.
|
Up to 12 months
|
|
Average score from the Readiness for Hospital Discharge Scale
Time Frame: Up to 12 months
|
A simple ANOVA model with floor as a fixed blocking factor treatment (TEPID or no TEPID) as a fixed factor.
Unit appears in the model as a nested factor within treatment, and statistical tests will be adjusted for this nesting structure.
The main test of interest in each model is the overall effect of treatment, which quantifies the effect of TEPID on the average score for the response.
P-values below 0.05 for this effect will be considered statistically significant.
|
Up to 12 months
|
|
Emergency department visits
Time Frame: Up to 12 months
|
A generalized linear model will be used for the binary responses (readmission and ED visit).
|
Up to 12 months
|
|
Patient satisfaction as measured by the Press Ganey Consumer Assessment of Healthcare Providers and Systems Survey
Time Frame: Up to 12 months
|
A simple ANOVA model with floor as a fixed blocking factor treatment (TEPID or no TEPID) as a fixed factor.
Unit appears in the model as a nested factor within treatment, and statistical tests will be adjusted for this nesting structure.
The main test of interest in each model is the overall effect of treatment, which quantifies the effect of TEPID on the average score for the response.
P-values below 0.05 for this effect will be considered statistically significant.
|
Up to 12 months
|
|
Readmission rates
Time Frame: Up to 12 months
|
A generalized linear model will be used for the binary responses (readmission and ED visit).
|
Up to 12 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Lisa Graham, Ohio State University Comprehensive Cancer Center
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- OSU-14237
- NCI-2016-01308 (REGISTRY: CTRP (Clinical Trial Reporting Program))
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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