We updated the design of this site on September 25th. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

IRF-PAI Functional Outcomes Data(With FIM Instrument Variables)

This study is ongoing, but not recruiting participants.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01779037
First Posted: January 29, 2013
Last Update Posted: October 28, 2016
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.
Information provided by (Responsible Party):
Uniform Data System for Medical Rehabilitation
  Purpose
IRF-PAI Functional Outcomes Data, including FIM instrument variables

Condition
Heart and Blood Disease Muscle, Bone and Cartilage Disease Nervous System Diseases Skin and Connective Tissue Disease Wounds and Injuries

Study Type: Observational [Patient Registry]
Target Follow-Up Duration: 1 Day
Official Title: IRF-PAI Functional Outcomes Data(With FIM Instrument Variables)

Further study details as provided by Uniform Data System for Medical Rehabilitation:

Primary Outcome Measures:
  • IRF-PAI Assessment Instrument(including the FIM instrument) [ Time Frame: admission/discharge ]

Study Start Date: January 2001
Estimated Primary Completion Date: December 2050 (Final data collection date for primary outcome measure)
Groups/Cohorts
Inpatient Rehabilitation Patients

Detailed Description:
United States IRF functional outcomes, medical and socio-demographic data for years 2002-2015
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   7 Years to 100 Years   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
inpatient rehabilitation patients
Criteria

Inclusion Criteria:

  • Admission to an inpatient rehabilitation facility

Exclusion Criteria:

  • Admission to acute, SNF setting, etc.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01779037


Locations
United States, New York
UDSMR
Buffalo, New York, United States, 14228
Sponsors and Collaborators
Uniform Data System for Medical Rehabilitation
  More Information

Additional Information:
Responsible Party: Uniform Data System for Medical Rehabilitation
ClinicalTrials.gov Identifier: NCT01779037     History of Changes
Other Study ID Numbers: IRFPAIdata
First Submitted: January 24, 2013
First Posted: January 29, 2013
Last Update Posted: October 28, 2016
Last Verified: October 2016

Additional relevant MeSH terms:
Nervous System Diseases
Wounds and Injuries
Connective Tissue Diseases
Hematologic Diseases
Cartilage Diseases
Musculoskeletal Diseases