Effects of Discharge Readiness on Success Following Discharge From Sub-Acute Rehab
NCT ID: NCT04010812
Last Updated: 2019-09-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
85 participants
OBSERVATIONAL
2019-06-13
2020-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Self-management Program for Patients in the Sub-acute Phase After Traumatic Injury - a Feasibility Study
NCT06093074
Stroke Home Health Aide Recovery Program (SHARP) Pilot
NCT04840407
Developing a Patient Oriented Discharge Summary for Stroke Inpatients
NCT03177954
Early Supported Discharge After Stroke in Bergen
NCT00771771
Use of Physical Therapy Outcome Measures to Predict Discharge Destination in People With Stroke From Acute Care Hospital
NCT07139444
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
CROSS_SECTIONAL
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Questionnaire
RHDS- Readiness For Hospital Discharge Scale, Patient Self-Assessment Form
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* consent with observed teach back confirmation
* discharge from sub-acute rehabilitation
Exclusion Criteria
* inability to "teach back" during consent process
* non english speaking
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Stony Brook University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Nancy Williams
Adjunct professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Peconic Landing
Greenport, New York, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
1352630-1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.