- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07265713
Bring Sleep to Life - Evaluation and Description of a Sleep Intervention in Emergency Care
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
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Stockholm, Sweden, 141 86
- Karolinska University Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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:
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:
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:
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
Sponsor
Investigators
- Study Chair: Linda Gellerstedt, RN, PhD, Karolinska Institutet
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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