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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04010812
Recruitment Status : Enrolling by invitation
First Posted : July 8, 2019
Last Update Posted : September 18, 2019
Sponsor:
Information provided by (Responsible Party):
Nancy Williams, Stony Brook University

Tracking Information
First Submitted Date June 14, 2019
First Posted Date July 8, 2019
Last Update Posted Date September 18, 2019
Actual Study Start Date June 13, 2019
Estimated Primary Completion Date June 30, 2020   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: July 5, 2019)
Number of falls, ER visits, hospitalization [ Time Frame: 30 days ]
Participant reported 30 days after discharge from rehabilitation facility
Original Primary Outcome Measures Same as current
Change History
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Effects of Discharge Readiness on Success Following Discharge From Sub-Acute Rehab
Official Title The Effects of Discharge Readiness on Success Following Discharge From Sub-Acute Rehab
Brief 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.
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.
Study Type Observational
Study Design Observational Model: Case-Only
Time Perspective: Cross-Sectional
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population Older adults discharged from a sub-acute rehabilitation facility
Condition Discharge From Sub-acute Rehabilitation Facility
Intervention Other: Questionnaire
RHDS- Readiness For Hospital Discharge Scale, Patient Self-Assessment Form
Study Groups/Cohorts Not Provided
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Enrolling by invitation
Estimated Enrollment
 (submitted: July 5, 2019)
85
Original Estimated Enrollment Same as current
Estimated Study Completion Date December 31, 2020
Estimated Primary Completion Date June 30, 2020   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

Montreal Cognitive Assessment score 22 or greater

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

Exclusion Criteria:

  • Montreal Cognitive Assessment score less than 22
  • inability to "teach back" during consent process
  • non english speaking
Sex/Gender
Sexes Eligible for Study: All
Ages Child, Adult, Older Adult
Accepts Healthy Volunteers Not Provided
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries United States
Removed Location Countries  
 
Administrative Information
NCT Number NCT04010812
Other Study ID Numbers 1352630-1
Has Data Monitoring Committee No
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement
Plan to Share IPD: Yes
Plan Description: Data Collection sheet
Responsible Party Nancy Williams, Stony Brook University
Study Sponsor Stony Brook University
Collaborators Not Provided
Investigators Not Provided
PRS Account Stony Brook University
Verification Date September 2019