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

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Uniform Data System for Medical Rehabilitation
ClinicalTrials.gov Identifier:
NCT01779037
First received: January 24, 2013
Last updated: August 26, 2014
Last verified: August 2014
  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)

Resource links provided by NLM:


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 ] [ Designated as safety issue: No ]

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 2002-2013

  Eligibility

Ages Eligible for Study:   7 Years and older
Genders Eligible for Study:   Both
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
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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:
No publications provided

Responsible Party: Uniform Data System for Medical Rehabilitation
ClinicalTrials.gov Identifier: NCT01779037     History of Changes
Other Study ID Numbers: IRFPAIdata
Study First Received: January 24, 2013
Last Updated: August 26, 2014
Health Authority: United States: Institutional Review Board

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

ClinicalTrials.gov processed this record on October 23, 2014