Effect of Functional Assessment and Immediate Rehabilitation of ED Admitted Elderly With Reduced Functional Performance
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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.
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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
Trial design
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Interventional model
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336 participants in 4 patient groups
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Data sourced from clinicaltrials.gov
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