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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: October 26, 2016
Last verified: October 2016
  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 ] [ 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 2002-2015
  Eligibility

Ages Eligible for Study:   7 Years to 100 Years   (Child, Adult, Senior)
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:
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: October 26, 2016
Health Authority: United States: Institutional Review Board

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

ClinicalTrials.gov processed this record on December 07, 2016