MedPath

The evaluation of a Dutch cardiology Primary Car Plus interventio

Recruiting
Conditions
Adult patients (&#8805
18 years) with non-acute and low-complexity cardiology-related health complaints
Registration Number
NL-OMON20762
Lead Sponsor
Maastricht University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
858
Inclusion Criteria

The study population consists of adult patients (≥18 years) with non-acute and low-complexity cardiology-related health complaints, registered with a GP in the region of the pioneer site. Based on the principles of shared decision-making the GP and the patient will discuss the options for referral which will be either the PC+ centre (intervention group) or the hospital-based outpatient cardiology care (control group). The decision will be based on expertise and experience of the GP, the severity of the complaints of the patient and the preferences of the patient. Less sever, non-acute and low-complex patients should be referred to PC+. At the moment, no specific criteria are included for the referral to PC+. The GP is in charge of referring a patient to the PC+ centre or the hospital-based outpatient cardiology care, i.e. the researchers do not have any influence on the referrals.

Exclusion Criteria

Excluded from participation are patients who are already diagnosed with cardiology-related health problems by a cardiologist and patients who have received balloon angioplasty or bypass surgery in the past 18 months. Furthermore, patients with acute health problems who require immediate hospital care and/or patients arriving at the emergency department of the hospital are excluded from participation.

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Triple Aim outcomes: <br /><br>- Health of the population<br /><br>- Quality of care<br /><br>- Healthcare costs
Secondary Outcome Measures
NameTimeMethod
A qualitative study that will consist of semi-structured interviews, focus groups and observations. Besides evaluating the process of the introduction of PC+ (e.g. identifying the barriers and facilitators), the aim of the qualitative study is to clarify and explain quantitative results. Therefore, the qualitative study will be based on an adaptive approach; the ultimate design will depend on developments during the research and results of the quantitative study.
© Copyright 2025. All Rights Reserved by MedPath