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Effect of Functional Assessment and Immediate Rehabilitation of ED Admitted Elderly With Reduced Functional Performance

Effect of Functional Assessment and Immediate Rehabilitation of ED Admitted Elderly With Reduced Functional Performance

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02062541
Enrollment
336
Registered
2014-02-13
Start date
2015-06-30
Completion date
2017-01-31
Last updated
2017-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Functionally-Impaired Elderly

Keywords

functional assessment, rehabilitation, cross-sectorial cooperation

Brief summary

Background: Illness and hospitalisation, even of short duration, pose separate risks for permanently reduced functional performance in elderly medical patients. Functional assessment in the acute pathway will ensure early detection of declining performance and form the basis for mobilisation during hospitalisation and subsequent rehabilitation. For optimal results rehabilitation should begin immediately after discharge. The aim of this study is to investigate the effect of a systematic functional assessment in the emergency departments (ED) of elderly medical patients with reduced functional performance when combined with immediate post-discharge rehabilitation. Method/design: The study is a two-way factorial randomised clinical trial. Participants will be recruited among patients admitted to the ED who are above 65 years of age with reduced functional performance. Patients will be randomly assigned to one of four groups: 1) functional assessment and immediate rehabilitation; 2) functional assessment and usual rehabilitation; 3) usual assessment and immediate rehabilitation; 4) usual assessment and usual rehabilitation. Primary outcome: 30-second chair-stand test administered at admission and two weeks after discharge. We hypothesise that such assessment in the ED or/and immediate rehabilitation will result in sustained or improved performance in comparison to regimen in which neither of these interventions are offered.

Interventions

OTHERFunct. assessment+fast rehabilitation
OTHERFunct. assessment+usual rehabilitation
OTHERusual assessment+fast rehabilitation

Sponsors

Sygehus Lillebaelt
CollaboratorOTHER
University of Southern Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* medical patients of 65 years of age or older admitted to the ED * Can speak and understand Danish * Resident in either of the two included municipalities * Can report personal data and decide on consent * Are able to sit on an chair and perform ≤ 9 repetitions at the 30-s. chair-stand test

Exclusion criteria

* Patients suffering from a progressive neurological or cognitive deficit or disease. * Patients ordinarily unable to walk

Design outcomes

Primary

MeasureTime frame
30-second-chair-stand testup to 14 days after admission date

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026