CClinicalTrials.gg
Status unknownNCT04010812Updated Sep 18, 2019

Effects of Discharge Readiness on Success Following Discharge From Sub-Acute Rehab

An observational study in Discharge From Sub-acute Rehabilitation Facility, sponsored by Stony Brook University. Status unknown at 1 site in United States. Per ClinicalTrials.gov, last updated 2019-09-18.

Sponsored by Stony Brook University · Observational

The sponsor has not verified this record recently (last verified Sep 2019), so the status shown — last known as Enrolling by invitation — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
85
Sex
All
01

Study summary

Study's purpose is to determine if a patient's perception of readiness for discharge from sub-acute rehabilitation, as measured by Readiness For Hospital Discharge Scale Patient Self-Reports Form, correlates with the patient's success after discharge, measured by patient reported number of falls, emergency room visits and hospitalizations 30 days post discharge.

Read the detailed description

All sub-acute rehabilitation patients will be approached for study participation one day prior to discharge day from the facility. Patients will be approached in their private room within the facility to obtain consent. Consent will be reviewed with patient by investigators. Patients will be asked to demonstrate understanding of the study and what consent will imply utilizing the teach back method. If patient is able to demonstrate understanding and gives consent the MoCA will be administered. If MoCA scores falls between 22-30 they will be included in study. If MoCA score falls below 22 they will not be included in study and that will be explained to them at that time. MoCA scores will be included in patient medical record. Patient name and assigned ID number, phone number, second contact and consent will be recorded on the confidential roster sheet and stored in a locked file cabinet located in director's office at Peconic Landing. The day of discharge patients will complete the RHDS survey. Investigators will complete the study data sheet including ID number, MoCA score, RHDS score, length of stay, discharge date, and recommended discharge therapy- home care, outpatient, none. Thirty to thirty-seven days after discharge investigators will call patient and ask 3 questions from scripted form. "How many falls have you had since discharge home:, "How many visits to the emergency room have you had since your discharge home","How many admissions to the hospital have you had since your discharge home." Following completion of telephone questions, confidential roster sheet and consent form will be shredded.

02

Conditions studied

  • Discharge From Sub-acute Rehabilitation Facility
03

In context

Lead sponsor

Stony Brook University is the lead sponsor of 191 studies on the registry; 36 are open to participants now.

Of its 22 completed or terminated interventional studies of FDA-regulated products, 10 (45%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Older adults discharged from a sub-acute rehabilitation facility

Inclusion criteria

Montreal Cognitive Assessment score 22 or greater

  • consent with observed teach back confirmation
  • discharge from sub-acute rehabilitation

Exclusion criteria

Exclusion Criteria:

  • Montreal Cognitive Assessment score less than 22
  • inability to "teach back" during consent process
  • non english speaking
05

Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
85 participants (estimated)
Patient registry
No

Interventions

  • OtherQuestionnaire

    RHDS- Readiness For Hospital Discharge Scale, Patient Self-Assessment Form

06

What researchers measure

Primary outcomes

  1. Number of falls, ER visits, hospitalization

    Participant reported 30 days after discharge from rehabilitation facility

    Time frame: 30 days

07

Study locations

1 site
  • Peconic Landing
    Greenport, New York 11944, United States
08

References and documents

Individual participant data

Plan to share: Yes — Data Collection sheet

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04010812
Lead sponsor
Stony Brook University
Responsible party
Nancy Williams (Adjunct professor, Stony Brook University) — Principal investigator
First posted
Jul 8, 2019
Start date
Jun 13, 2019
Primary completion
Jun 30, 2020 (estimated)
Completion
Dec 31, 2020 (estimated)
Last update
Sep 18, 2019

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2019. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion