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OpenTrials
Completed

NCT Number: NCT02062541

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

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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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Lillebaelt hospital

Kolding, 6000, Denmark

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Funct. assessment+fast rehabilitation

Other

Funct. assessment+usual rehabilitation

Other

usual assessment+fast rehabilitation

Other

Primary outcomes

  1. 30-second-chair-stand test

    Time frame: up to 14 days after admission date

Sponsors and collaborators

Lead sponsor

University of Southern Denmark

Other

Collaborators

  • Sygehus Lillebaelt

Registry information

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
Feb 13, 2014
Registry last updated
Feb 2, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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