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Completed

NCT Number: NCT02899208

Can an Actigraph be Used to Predict Physical Function in Intensive Care Patients?

This study aims to investigate whether an actigraph, measuring in-hospital activity, used for a week after discharge from the ICU at Zealand University Hospital Køge, can predict physical function at three-month follow up.

The hospital activity will be measured with actigraphy, a measurement tool that quantifies activity level. The activity will be measured for 7 days after ICU discharge. The actigraph is to be worn as a bracelet.

The physical function will be measured with Chelsea Critical Care Physical Assessment Tool (CPAx). CPAx is assessed at ICU discharge and after three months.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Zealand University Hospital

Køge, 4600, Denmark

About this study

Treatment at an Intensive Care Unit (ICU) is often needed for the survival of critically ill patients, but it can take a long time to recover. A number of high quality studies have shown that patients experience functional impairments for a long period after discharge, even for years.

These patients may suffer from a number of other negative influences of their critical illness and ICU stay, e.g. memory problems, episodes of depression, cognitive dysfunction and sleeping disorders. These symptoms are seen in both medical and surgical patients and has been named the Post Intensive Care Syndrome.

Physical rehabilitation is important and must start already during admission, in order to regain some of the function and independence of the patients. This has a well documented effect on both mental and physical wellbeing.

Actigraphy is a newer way of quantifying the activity level continuously. It is validated and has been used in the ICU to assess agitation and sedation and in an oncological, surgical and even an ICU population to assess sleep.

It is easy to use, non-invasive and inexpensive. It is worn like a bracelet and doesn't impair the patients mobility or ambulation.

Another issue when evaluating physical impairments is the choice of method for assessing physical function. For this study, the investigators use the Chelsea Critical Care Physical Assessment Tool (CPAx) as it has good validity and clinimetric properties and is easy to use. Also, it can be done as part of the daily training as it is developed specifically for the ICU.

The aim of this study is to investigate how the in-hospital activity level of patients after ICU discharge is associated with their physical function at three months post discharge.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients > 18 years of age
  • Admitted to the ICU for > 24 h

Exclusion criteria

  • Not able to speak and understand Danish
  • Patients suffering from dementia or psychosis
  • Discharged from the ICU to terminal care
  • Patients transferred to another hospital during ICU stay
  • Patients living outside the Region of Zealand
  • Patients suffering from total paralysis before admission

Treatment and study plan

Primary outcomes

  1. The association between actigraph levels and CPAx at three months after discharge from ICU

    Time frame: 3 months after discharge from intensive care unit

    The association between actigraph levels and CPAx score (from 0 to 50 points)

Secondary outcomes

  1. CPAx at discharge from ICU

    Time frame: Within 24 hours of discharge from intensive care unit

    CPAx score (from 0 to 50 points)

  2. Activity measured with actigraph during one week after ICU-discharge

    Time frame: One week after discharge from ICU

    Activity measured with an actigraph watch placed on the patients' wrist

  3. Association between early activity level measured with actigraphy for 7 days and SF 36 at three months after discharge from ICU

    Time frame: 3 months after discharge from intensive care unit

    The association between actigraph levels and SF-36 score

  4. Association between early activity level measured with actigraphy for 7 days and Hospital Anxiety and Depression Scale (HADS) at three months after discharge from ICU

    Time frame: 3 months after discharge from intensive care unit

    The association between actigraph levels and HADS score (from 0 to 42 points)

  5. Association between early activity level measured with actigraphy for 7 days and Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) at three months after discharge from ICU

    Time frame: 3 months after discharge from intensive care unit

    The association between actigraph levels and RBANS score

  6. Association between early activity level measured with actigraphy for 7 days and mortality within hospital stay, after ICU discharge

    Time frame: The period within hospital stay, after intensive care unit discharge

    The association between actigraph levels and hospital mortality

  7. Association between early activity level measured with actigraphy for 7 days and mortality within 90 days after ICU discharge

    Time frame: 3 months after discharge from intensive care unit

    The association between actigraph levels and 90-day mortality

  8. Association between early activity level measured with actigraphy for 7 days and consumption of opioids (strong/weak) at 90 days follow up.

    Time frame: 3 months after discharge from intensive care unit

    The association between actigraph levels and opioid-consumtion (morphine-equivalents)

Sponsors and collaborators

Lead sponsor

Zealand University Hospital

Other

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Sep 14, 2016
Registry last updated
Jul 2, 2017

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

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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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