Heart and Blood DiseaseNCT01779037
IRF-PAI Functional Outcomes Data(With FIM Instrument Variables)
An observational study of Heart and Blood Disease and Muscle, Bone and Cartilage Disease, run by Uniform Data System for Medical Rehabilitation at 1 site in United States.
Trial summary
IRF-PAI Functional Outcomes Data, including FIM instrument variables Read more about this study
- Who is it for?
- Ages 7 to 100 years
- Conditions the study is for
- Heart and Blood Disease, Muscle, Bone and Cartilage Disease, Nervous System Diseases
- How many people
- Not given
- Where
- 1 siteUnited States
- Study dates
- Jan 2001to 1 May 2018
- How long will I take part?
- 1 Day
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 7 to 100 years
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: inpatient rehabilitation patients
Who may be able to join
- Admission to an inpatient rehabilitation facility
Who cannot join
- Admission to acute, SNF setting, etc.
Trial locations and contacts
1 site in 1 country.
About this study
IRF-PAI Functional Outcomes Data, including FIM instrument variables
Read the detailed description
United States IRF functional outcomes, medical and socio-demographic data for years 2002-2015
- Conditions
- Heart and Blood Disease, Muscle, Bone and Cartilage Disease, Nervous System Diseases, Skin and Connective Tissue Disease, Wounds and Injuries
- Medical subject headings
- Hematologic Diseases, Cartilage Diseases, Nervous System Diseases, Connective Tissue Diseases, Wounds and Injuries
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Inpatient Rehabilitation Patients | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
IRF-PAI Assessment Instrument(including the FIM instrument)
Measured: admission/discharge
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 Jan 2013 (estimated)
- Study startJan 2001
- Primary completion1 May 2018
- Study completion1 May 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Heart and Blood DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Other
- Target duration
- 1 Day
Sponsor and investigators
- Lead sponsor
- Uniform Data System for Medical Rehabilitation
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01779037
- Sponsor's protocol ID
- IRFPAIdata
- Status last verified
- May 2018
- First submitted
- 24 Jan 2013
- Last updated
- 4 May 2018
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 4 May 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- IRF-PAI Functional Outcomes Data(With FIM Instrument Variables)
- ClinicalTrials.gov ID
- NCT01779037
- Acronym / sponsor ID
- IRFPAIdata
- Conditions
- Heart and Blood Disease, Muscle, Bone and Cartilage Disease, Nervous System Diseases, Skin and Connective Tissue Disease, Wounds and Injuries
- Study type
- Observational
- Recruitment status
- Terminated
- Lead sponsor
- Uniform Data System for Medical RehabilitationUniversity, hospital or other
- Study start
- Jan 2001
- Primary completion
- 1 May 2018 (actual)
- Study completion
- 1 May 2018 (actual)
- First posted
- 29 Jan 2013 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
IRF-PAI Functional Outcomes Data, including FIM instrument variables
Detailed description
United States IRF functional outcomes, medical and socio-demographic data for years 2002-2015
Study design
- Observational model
- Other
- Time perspective
- Other
- Target follow-up
- 1 Day
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Inpatient Rehabilitation Patients | – | – |
Who may qualify
- Ages
- 7 to 100 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- inpatient rehabilitation patients
Key inclusion criteria (1 listed)
- Admission to an inpatient rehabilitation facility
Key exclusion criteria (1 listed)
- Admission to acute, SNF setting, etc.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
IRF-PAI Assessment Instrument(including the FIM instrument)
Time frame: admission/discharge
Results and safety
The study was stopped early. Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 May 2018.
- Related InfoLink provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Heart and Blood Disease and Muscle, Bone and Cartilage Disease, run by Uniform Data System for Medical Rehabilitation at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 4 May 2018. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was stopped early. Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
IRF-PAI Assessment Instrument(including the FIM instrument) (time frame: admission/discharge). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 May 2018.