RecruitingACTRN12614000616673

The effect of modified night lighting on sleep characteristics, and activity levels among admitted inpatients.

A prospective observational study among admitted inpatients evaluating the effects of a modified night lighting intervention on patient sleep characteristics, activity levels, and related environmental variables compared with patients in rooms where the modified night lighting is absent.


Sponsor

Royal Brisbane and Women's Hospital

Enrollment

84 participants

Start Date

Jun 12, 2014

Study Type

Observational

Conditions

Summary

This study will explore the influence of modified night lighting installed in specific locations within hospital patient rooms and toilets, on how well patients sleep, how they move about at night and the effect of the lighting on other related aspects of the environment (such as the use of other forms of lighting at night). The modified lighting is being implemented as part of a larger study, a cluster randomised controlled trial across six RBWH wards, examining whether improved night lighting reduces the number of patient falls on these wards. By collecting this additional data directly from patients before and after the lighting is installed, the current observational study will allow us to compare whether there are differences at the patient-level between control and intervention environments.


Eligibility

Sex: Both males and femalesMin Age: 65 Yearss

Plain Language Summary

Simplified for easier understanding

This companion study to a hospital falls prevention trial is looking more closely at how modified night lighting in patient rooms affects how well individual patients sleep and how much they move around at night. Patients admitted to one of six study wards will be asked about their sleep quality and experiences before and after the new lighting is installed, helping researchers understand whether the lighting actually improves comfort and rest for patients. You may be eligible if: - You are 65 years of age or older - You are admitted to one of the six study wards at Royal Brisbane and Women's Hospital - You have been on the ward for fewer than 30 days - You are not due to be discharged within 3 days - You speak fluent English You may NOT be eligible if: - You have known cognitive impairment - You are not fluent in English - You are too unwell or medically unstable to participate - You have already provided data for this study in a previous month Talk to your doctor about whether this trial might be right for you.

This is a simplified summary. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

In this study, we intend to observe the patient-level effects of a night lighting intervention being implemented as part of a separate study, a stepped wedge cluster randomised controlled trial across

In this study, we intend to observe the patient-level effects of a night lighting intervention being implemented as part of a separate study, a stepped wedge cluster randomised controlled trial across six wards at the Royal Brisbane and Women's Hospital (RBWH) - ANZ trial registration ID: ACTRN12614000615684. The cluster RCT examines the effect of the intervention on ward level inpatient fall rates. The observational study described here will additionally examine the effect of the modified environment on other patient level effects, specifically sleep and activity levels. Here, we will recruit one patient per ward per month across the 14 month period of the cluster RCT (84 patients in total to be recruited). It is anticipated that across the 14 month trial period, 42 patients will be exposed to the modified environment. At the initial interview (baseline) we will ask participants to rate their visual impairment, hearing impairment, pre-admission sleepiness and sleep behaviour, current levels of sleepiness, sleep behaviour and insomnia, causes of current sleep disruption and current functional status. After the initial interview, we will follow-up participants on day three, seven and twelve (+/- one day) unless discharged from hospital or transferred out of the room earlier,. We will ask patients to rate current levels of sleepiness, sleep behaviour and insomnia, current functional status, and causes of sleep disruption over preceding days. We will also ask participants to rate their satisfaction with the physical environment and suggestions for improvements in the physical environment to support patient sleep and mobility. In addition to the above measures, we will collect continuous data on patient activity levels and light exposure through the use of a wrist worn actigraph (maximum of 12 days from initial interview). Over the same period, we will collect continuous data on environmental light variation in the room and bathroom through the use of a wall-mounted light sensing data logger. Opening and closing of the toilet door will be collected using a simple state change data logger.


Locations(1)

Royal Brisbane & Womens Hospital - Herston

QLD, Australia

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ACTRN12614000616673