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Not yet recruiting NCT03049865

Gait Speed at Discharge as a Marker for Readmission

Observational All Disease That May Require Acute Hospitalization Except for Phsychiatric Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: All Disease That May Require Acute Hospitalization Except for Phsychiatric Disease. Basic parameters: from 51 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Gait Speed at Discharge as a Marker for Readmission - The GASP Study

Overview

The principal aim is to assess if a simple test, the time it takes to walk 10 meters for a patient about to be discharged after a hospital stay for an acute illness, is related to the risk of readmission.

Primary outcome measures

  • Readmission [Time frame: 30 days]
Secondary outcome measures (2)
  • Readmissions [Time frame: 90,180, 365 days]
  • All-cause mortality [Time frame: 6, 12, 24, 36, 60 months]

Eligibility criteria

Inclusion criteria

  • >50 years of age Patient discharged to home, or temporary short stay nursing home Expected survival >90 days The ability to read or understand the instructions and to give informed consent.

Exclusion criteria

  • Planned hospital stay, i.e. the patient was admitted electively The including investigator is directly involved in the care of the patient

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT03049865 · Dnr 2016/2174-31

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗