- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06298240
Implementation of Nursing Demand Management as a Factor for Improvement in a Primary Care Emergency Center.
The Implementation of Nurse Demand Management as a Factor in Improving the Quality of Care in a Primary Care Emergency Center.
Background: Nurse Demand Management was born in 2009 out of the need to address the growth of spontaneous acute demand in primary care. But it is not until 2013 that guidelines for the exercise of nursing actions in demand management were established in Catalonia, Spain. Nurses trained specifically to solve acute and low complexity health problems generate a quality of care comparable to that provided by family medicine doctors. On the other hand, it is worth highlighting the need to rationalise medical resources in primary care centres, primary care emergency centres or points of continuous care (different emergency facilities in the territory in terms of size and services) in order to give priority to doctors being able to dedicate more time to medium or high complexity pathology. Although nurse demand management has been implemented in primary care teams for years, it is being carried out in different intensities according to the needs or priorities of each health territory.
The promotion of the autonomous role of nursing through the implementation of nurse demand management in the urgent spontaneous demand of low complexity can be transcendent, both in the optimisation of health resources in primary care and in the management of the demand for care.
Hypothesis: The implementation of nurse demand management is a factor of improvement in the efficiency and quality of care in the Primary Care Emergency Centre of the city of Mataró (Barcelona, Spain). Objectives: The main objective of this study was to determine whether the implementation of nurse demand management is a factor in improving efficiency and quality of care in the CUAP of Mataró. Methodology: Non-randomised controlled experimental intervention study. Application of a consensual guide with 5 reasons for health consultations where demand management nursing can be applied.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Barcelona
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Mataró, Barcelona, Spain, 08301
- Mataró primary care emergency center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- All users who come to the emergency centre between Monday and Friday (excluding public holidays) from 8 a.m. to 8 p.m. and who consult for the 5 possible health problems that are part of the study protocol.
Exclusion Criteria:
- Any spontaneous user or user referred by another health centre who comes for a re-consultation for the same health problem in less than 30 days will be excluded.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Consensuated nurse intervencion group
Application of a consensual nursing guide with 5 reasons for health consultation where an autonomous role can be applied.
Users who come to the emergency center during the first fifteen days of each month are assigned to the experimental group until the necessary sample of 156 subjects is reached.
|
An agreed nursing procedure is applied for users of a primary care emergency center who spontaneously consult for 5 acute health problems of low complexity: gastroenteritis, cystitis in women, dental pain, upper respiratory tract affections and acute wounds
|
|
No Intervention: Usual medical visit group
Users who come to the emergency center in the second fortnight of each month are assigned to the non-intervention (control) group where the usual medical visit is applied until the required sample of 156 subjects is reached.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Waiting time and resolution of the visit
Time Frame: During the entire process of assistance to the participant, an average of 4 hours.
|
Different time points are collected to analyze the duration of care at the center: time of entry into the triage consultation, time of entry into the medical or nursing consultation, and time of departure from the consultation. Time that the administrator receives the user and includes him/her in the work agenda of the emergency center. Time the user makes the triage. Time that the user is attended in the agenda of the demand management center (experimental group days). Time that the user is seen in the medical office (control group days). |
During the entire process of assistance to the participant, an average of 4 hours.
|
|
Number of reconsultations
Time Frame: 30 days
|
Number of return visits for the same health problem made by the participant in the subsequent 30 days.
|
30 days
|
|
patient experience
Time Frame: On a scale from 0 to 10, where 0 is not very satisfied and 10 is very satisfied.
|
Participant satisfaction survey, on the same day, of the care received by the doctor or nurse From 15 days after the hearing, a quality telephone survey will be conducted with all recruited subjects.
|
On a scale from 0 to 10, where 0 is not very satisfied and 10 is very satisfied.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Triage time
Time Frame: From 0 minutes to 4 hours
|
Entry time of the participant in the center's triage consultation.
The registered time is the one that appears in the electronic health record.
|
From 0 minutes to 4 hours
|
|
Entrance participating in the visit
Time Frame: From 0 minutes to 4 hours
|
Entrance to a doctor's or nurse's consultation.
The registered time is the one that appears in the electronic health record.
|
From 0 minutes to 4 hours
|
|
Participant exit of the visit
Time Frame: From 0 minutes to 4 hours
|
Time of departure of the participant from the medical or nursing consultation.
The registered time is the one that appears in the electronic health record.
|
From 0 minutes to 4 hours
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prescribed drugs
Time Frame: 0 to 10
|
number of drugs
|
0 to 10
|
|
Processed labour disabilities
Time Frame: 0 to 1
|
Number of processed labour disabilities
|
0 to 1
|
|
Diagnoses change
Time Frame: 0 to 1
|
Diagnoses change at the visits for the same health problem fort the next month
|
0 to 1
|
Collaborators and Investigators
Investigators
- Principal Investigator: Jordi Estarlich Corominas, IP, Active nurse in the emergency center where the study is carried out
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 4R22/074
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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