Bring Sleep to Life - Evaluation and Description of a Sleep Intervention in Emergency Care

November 24, 2025 updated by: Arja Vehkala Höglund, Karolinska University Hospital

Many patients complain of poor sleep during their hospital stay. Therefore, we want to investigate how we can improve the staff's (nurses and assistant nurses) knowledge about sleep and which nursing interventions can lead to improved sleep during their hospital stay.

The intervention are in three parts:

a clinical guideline introduction of sleep nursing champions a web-based educational course

Study Overview

Detailed Description

A majority of hospitalised have reported being awakened due to external factors, of which being disturbed by hospital staff was the most common. It is therefore essential to provide nursing staff with the knowledge and tools to promote patients' sleep during hospitalisation. For this purpose, an intervention was developed to aid nursing staff in adopting evidence-based, non-pharmacological methods to promote sleep. The intervention comprises three parts: a web-based educational course, a clinical guideline and the introduction of sleep nursing champions (SNCs) at the intervention units.

Study Type

Interventional

Enrollment (Estimated)

300

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Stockholm, Sweden, 141 86
        • Karolinska University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Sleep nursing champions (SNCs):

Inclusion Criteria:

  • Registered nurse with area responsibility for sleep
  • Held the assignment for responsibility for sleep at least six months.
  • Working at Theme Heart, Vascular and Neurology in Karolinska University Hospital

On-line survey staff:

Inclusion Criteria:

• Clinically active staff (nurse, assistant nurse) at the intervention departments within Theme Heart, Vascular and Neurology

Control group:

Inclusion Criteria:

  • Clinically active staff (nurse, assistant nurse) at Theme Cancer Karolinska University Hospital
  • No access to the guideline for sleep, and digital sleep education programme

Patients´ experiences:

Inclusion Criteria:

  • Hospitalized for at least one night in the intervention departments
  • Understand the Swedish language both spoken and written
  • Age over 18 years

Exclusion Criteria:

  • Diagnosis of cognitive impairment
  • Delirium
  • Failing vital parameters as low blood pressure
  • Severe visual impairment that makes it impossible to complete the questionnaire

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Introduction of sleep nursing champions (SNCs)
To describe sleep nurses' experiences of working with sleep-promoting nursing and to describe their experiences of having sleep as an area of responsibility within nursing.
The sleep guideline has been available since 2021, but it is unknown whether healthcare professionals are aware of this guideline. And whether it is used in clinical practice.
The web-based interactive sleep training course to increase knowledge about sleep for hospital staff.
Other: Sleep guideline and web-based sleep training education
On-line survey to evaluate the introduction of a sleep guideline and a web-based sleep training aimed at staff in nursing wards.
The sleep guideline has been available since 2021, but it is unknown whether healthcare professionals are aware of this guideline. And whether it is used in clinical practice.
The web-based interactive sleep training course to increase knowledge about sleep for hospital staff.
No Intervention: Patients experience
On-line survey description from patients' perspectives about sleep in connection with hospital care.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Description of the role of a sleep nurse champions (SNC)
Time Frame: Individual interviews on one occasion. Time required max. 60 minutes. Total 13 SNC.

Individual semi-structured interviews with sleep nursing champions (SNC) to investigate their experience about the role as SNC:

  • Description of the tasks as a SNC.
  • Identify characteristics that are important for being a SNC
  • Identify success factors in the assignment
  • Identify obstacles or setbacks in the assignment
  • Identify the areas of nursing that are important to develop to promote patients' sleep
  • Need for sleep as an area of nursing
  • Existence of support from your immediate manager, colleagues, other professional groups or the project group.
  • Changes in how you think patients' sleep is affected by the introduction of a SNC in your department
  • Perceptions of patients' sleep in connection with hospital care
  • SNC knowledge of sleep and health-related quality of life linked and how.

We also collect demographic data: age of participants, number of years as a nurse, employed at department and orks: day or three shifts or night only.

Individual interviews on one occasion. Time required max. 60 minutes. Total 13 SNC.
Web-based survey on sleep knowledge and awareness of online sleep training and sleep guidelines
Time Frame: The survey is completed once. It takes approximately 15 minutes.

The survey consists of questions about:

Intervention units:

  • General knowledge about sleep and factors that affect patients' sleep in hospitals
  • Specific sleep questions about sleep and sleep-promoting measures according to the online training program and guideline
  • If sleep is prioritized in the clinic and for the individual.

Control units:

• General questions about sleep and sleep-promoting measures in acute care.

There is also the possibility to develop the answers given in the survey through so-called free text answers.

We also collect demographic data: professional title/profession, number of years in the profession, age, gender, and which theme/department you work in.

At the intervention units we also collect data about whether you have completed sleep training, and whether you have read the sleep guideline.

The survey is completed once. It takes approximately 15 minutes.
Inpatients' experiences of sleeping in hospital
Time Frame: The questionnaire is completed once during the hospitalisation. Time required is a maximum of 20-30 minutes.

Web-based or printed paper questionnaire survey:

  • Increase knowledge about patients' experiences of sleep in hospitals.
  • Investigate patients' experiences of staff's work to promote patients' sleep.

There is also the possibility to develop the answers given in the survey through so-called free text answers.

We also collect demographic data as: date of birth, gender, marital status, education level, use of sleep medication, hospital ward, single or multi-bed room.

The questionnaire is completed once during the hospitalisation. Time required is a maximum of 20-30 minutes.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Linda Gellerstedt, RN, PhD, Karolinska Institutet

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 15, 2024

Primary Completion (Estimated)

March 1, 2026

Study Completion (Estimated)

May 1, 2026

Study Registration Dates

First Submitted

November 17, 2025

First Submitted That Met QC Criteria

November 24, 2025

First Posted (Actual)

December 5, 2025

Study Record Updates

Last Update Posted (Actual)

December 5, 2025

Last Update Submitted That Met QC Criteria

November 24, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • Dnr 2023-04670-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

All IPD that underlie results in a publication

IPD Sharing Time Frame

2026 January - 2027 December

IPD Sharing Access Criteria

Everyone who asked for supporting information.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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