- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04367298
Chronoprevention in Hospital Falls of Older People (CHRONOFALLS)
Chronoprevention in Hospital Falls of Older People: A Nursing Intervention CHRONOFALLS
Accidental falls in hospitals are serious events concerning the safety of the patients. Recent studies demonstrated that the time of falls is a key factor to be considered in prevention. It has been shown that the time of day, the day of the week and the month of the year impact on the occurrence of falls.
The aim of this project is to know the effect of the application of a program of preventive measures based on the temporal patterns of the risk factors on the hospital fall occurrence. A mixed method research design will be conducted. Three phases will be carry out: 1) Longitudinal prospective study in two parts: a) audits and seminars of health professionals focused on an effective and efficient hospital falls register. Cosinor and Multi-Component analyses will be performed to obtain temporal patterns of the hospital falls and their related variables. b) Implementation of a based-temporal patterns, multidimensional prevention program. 2) Retrospective study of falls registered in institutional databases. 3) Qualitative study based on focus groups (physicians, nurses and nursing assistants).
It is imperative to study temporal patterns of hospital falls to effectively and comprehensively define the etiology of falls, and therefore, design preventive strategies. A reduction of the number of in-hospital falls and related injuries is expected, as well as, an improvement of the quality of life of patients. Considering temporal patterns, and levels of mood and sleep of healthcare professionals will achieve an improvement of patient safety.
Study Overview
Detailed Description
-Design
A mixed-method research will be carried out. Three different study design will be used:
Phase 1. Prospective longitudinal study in 2 steps:
- A first step, of 18 months, in which a first intervention of audits and seminars in health professionals will be carried out, focused on an effective and efficient registry of hospital falls in older people. This first phase is crucial to identify temporal patterns of falls in relation to specific intrinsic and extrinsic risk factors among hospitalized older people; as well as the levels of fatigue/sleepiness, attention and cognitive functionality of the health professionals who attend to an in-hospital fall.
- A second step, of application of a multidimensional prevention program for 15 months focused on organizational, educational and behavioral elements; applied to admitted older people and health professionals.
Phase 2. Retrospective study of the fall records found in the institutional databases of the study centers, in the period between January 2018 - September 2020. This period covers the first (January 2018 - May 2019) and the second phase (June 2019 - September 2020) of the project, previously indicated.
Phase 3. Descriptive exploratory study with a qualitative approach, focus groups made up of health professionals: doctors, nurses and nursing assistants who provide and have provided their professional services in the field of study, in the periods in which the studies have been carried out. longitudinal and retrospective previously mentioned.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Córdoba, Spain, 14004
- Maimónides Biomedical Research Institute of Córdoba
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria in patients:
- Patients who suffer a hospital fall
- Accept and sing the informed consent
Exclusion Criteria in patients:
- Do not accept and sign the informed consent
Inclusion Criteria in healthcare professionals:
- Nurses in charge of the care of patients who suffer a fall
- Accept and sing the informed consent
Exclusion Criteria in patients:
- Nurses who do not care for a patient suffering a fall
- Do no accept and sign the informed consent
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Chronoprevention in hospital falls
Implementation of a hospital preventive measures program: adjusted to the identification of temporal patterns of falls and relative risk factors of falls.
|
Preventive measures will be focused on organizational, educational and behavioural elements related to older people and healthcare professionals
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Participant with Hospital falls
Time Frame: Through study completion, an average of 1 month
|
Records of falls coded in the International Classification of Diseases (ICD-10) between codes W00-W19.9
|
Through study completion, an average of 1 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Chronotype of patient
Time Frame: Through study completion, an average of 1 month
|
Morningness-Eveningness according to Horne-Östberg Questionnaire (1976).
Scores can range from 18-86.
Scores of 41 and below indicate "evening types".
Scores of 59 and above indicate "morning types".
Scores between 42 and 58 indicate "intermediate types".
|
Through study completion, an average of 1 month
|
|
Quality of life of patient
Time Frame: Through study completion, an average of 1 month
|
Short Form 36 Health Survey (SF-36) (Spanish version 2) (Alonso et al. 1996).
The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section.
Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight.
The lower the score the more disability.
The higher the score the less disability.
|
Through study completion, an average of 1 month
|
|
General health status of patient
Time Frame: Through study completion, an average of 1 month
|
28-Item General Health Questionnaire (GHQ28) (Spanish version) (Lobo et al. 1985).
Scores can range from 0-84.
Higher GHQ-28 scores indicate higher levels of distress
|
Through study completion, an average of 1 month
|
|
Sleep pattern of the healthcare professionals
Time Frame: Through study completion, an average of 1 month
|
Pittsburgh Sleep Quality Index (Spanish version) (Macías & Royuela, 1996).
Score can range from 0-21 with the higher total score indicating worse sleep quality.
|
Through study completion, an average of 1 month
|
|
Chronotype of the healthcare professionals
Time Frame: Through study completion, an average of 1 month
|
Chronotype according to Horne-Östberg Questionnaire (1976).
Scores can range from 18-86.
Scores of 41 and below indicate "evening types".
Scores of 59 and above indicate "morning types".
Scores between 42 and 58 indicate "intermediate types".
|
Through study completion, an average of 1 month
|
|
Quality of life of the healthcare professionals
Time Frame: Through study completion, an average of 1 month
|
Short Form 36 Health Survey (SF-36) (Spanish version 2) (Alonso et al. 1996).
The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section.
Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight.
The lower the score the more disability.
The higher the score the less disability.
|
Through study completion, an average of 1 month
|
|
General health status of the healthcare professional
Time Frame: Through study completion, an average of 1 month
|
28-Item General Health Questionnaire (GHQ28) (Spanish version) (Lobo et al. 1985).
Scores can range from 0-84.
Higher GHQ-28 scores indicate higher levels of distress
|
Through study completion, an average of 1 month
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Pablo Jesús López Soto, PhD, Maimónides Biomedical Research Institute of Córdoba
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Keywords
Other Study ID Numbers
- PI-0360-2017
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
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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