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Clinical Trials/NCT01599689
NCT01599689CompletedNot Applicable

Can an Evidence-based Mirrors Intervention Reduce Postoperative Delirium in Older Cardiac Surgical Patients? A Pilot and Feasibility Cluster Randomised Controlled Trial

Papworth Hospital NHS Foundation Trust2 sites in 1 country223 target enrollmentStarted: October 2012Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
223
Locations
2
Primary Endpoint
Delirium incidence

Study Overview

Brief Summary

This pilot cluster-randomised controlled trial aims to determine whether the use of bedside mirrors, as a clearly defined part of patients' postsurgical ICU care, can reduce delirium and improve outcomes in the older cardiac surgical patient.

Detailed Description

The risk of delirium, an acute disturbance in mental status and cognition that occurs commonly after cardiac surgery, increases sharply from the age of about 65 years. Its occurrence, even for one day, is associated with longer ICU and hospital stays, increased costs, and negative physical and cognitive outcomes at one year. In spite of previous prevention and intervention research, delirium incidence in the older cardiac surgical patient remains high (up to 72%).

ICU clinicians at Papworth Hospital have made observations suggesting that delirium could be reduced using a novel and unconventional strategy of bedside mirrors. Mirrors of any type are uncommon in ICU environments[1], but their occasional use by patients on our ICU has been reported by bedside clinicians and physiotherapists to result in:

  • a normalisation of mental status and attention (core delirium diagnostic criteria), and
  • earlier physical mobilisation (associated with reduced delirium risk), particularly in older-aged patients

Evidence from other sources supports mirrors' beneficial effect in these areas [2-10], but mirror use has never to our knowledge been explored for the reduction of delirium. This pilot study seeks to determine whether the use of bedside mirrors, as a clearly defined part of patients' postsurgical ICU care, can reduce delirium and improve outcomes in the older cardiac surgical patient.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
70 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • scheduled for elective or urgent cardiac surgery at Papworth Hospital
  • aged 70+ years

Exclusion Criteria

  • inability to obtain informed consent
  • care pathway anticipating admission elsewhere than to ICU following surgery
  • severe visual impairment impeding ability to recognise self in mirror
  • physical or communication barriers likely to impede effective administration of study procedures
  • severe mental disability likely to impede effective administration of study procedures or assessment of delirium
  • history of psychiatric illness previously requiring hospitalisation

Outcomes

Primary Outcomes

Delirium incidence

Time Frame: Assessed from day of ICU admission after surgery until day of ICU discharge (or until 12 weeks after surgery, whichever comes first)

Delirium will be measured twice daily, using the Confusion Assessment Method for the ICU (CAM-ICU).

Secondary Outcomes

  • Mental Status(Assessed from day of ICU admission after surgery until day of ICU discharge (or until 12 weeks after surgery, whichever comes first))
  • Attention(Assessed from day of ICU admission after surgery until day of ICU discharge (or until 12 weeks after surgery, whichever comes first))
  • Functional Independence(Assessed at 12 weeks after surgery)
  • Delirium time of onset(Assessed from day of ICU admission after surgery until day of ICU discharge (or until 12 weeks after surgery, whichever comes first))
  • Delirium duration(Assessed from day of ICU admission after surgery until day of ICU discharge (or until 12 weeks after surgery, whichever comes first))
  • Perceptual disturbances about the body and dissociative symptoms(Assessed at 12 weeks after surgery)
  • Health-Related Quality of Life (HRQoL)(Assessed at 12 weeks after surgery)
  • Length of ICU and hospital stay(Assessed at hospital hospital discharge)
  • Mortality(Assessed at 12 weeks after surgery)
  • Factual memories from ICU(Assessed at 12 weeks after surgery)
  • Intraclass correlation coefficient (ICC) for time clusters(Assessed from day of ICU admission after surgery until day of ICU discharge (or until 12 weeks after surgery, whichever comes first))
  • Acceptability of the intervention(Assessed from day of ICU admission after surgery until day of ICU discharge (or until 12 weeks after surgery, whichever comes first))

Investigators

Sponsor Class
Other Gov
Responsible Party
Sponsor

Study Sites (2)

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