Work-Related Frustration and Higher Cardiovascular Risk Blood Pressure Profiles

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age40-65
SponsorUniversity of Burgundy

About this trial

Background: Mental health is a national priority in France, especially in the workplace. The impact of poor quality of life at work on mental health has been demonstrated. Raising awareness of the importance of prevention within companies and the influence of working conditions seems essential. In the context of limited occupational health physicians, inherent access difficulties, and reduced resources, physical health is often addressed as the first line of intervention. In the Burgundy region, the prevention of cardiovascular diseases is a regional public health concern. A significant association has been found between effort/reward imbalance and masked hypertension. Identifying a link between working conditions, blood pressure profile, and thus increased cardiovascular risk would be relevant.

Objectives: The main goal of this observational study is to compare the frequency of blood pressure profiles at higher risk of cardiovascular events (white coat hypertension and daytime and/or nighttime masked hypertension) according to work-related quality of life and perceived stress levels among primary care patients without a history of hypertension or cardiovascular disease, in two departments of the Burgundy region.

Methods: This project is a proof-of-concept study before intervention on work-related quality of life and blood pressure profiles at higher cardiovascular risk in primary prevention. It is a prospective, interventional, and multicenter study, conducted from May 2023, across three multidisciplinary primary care centers, involving fifteen general practitioners from Côte d'Or and Saône-et-Loire. Patients aged 40 to 65, consulting one of the participating general practitioners, actively working, with no cardiovascular history or antihypertensive treatment, will be included. Work-related quality of life and perceived stress will be assessed using the QualTra-Scale and the PSS-10 scale, respectively. All included patients will undergo 24-hour ambulatory blood pressure monitoring (ABPM) during a workday. A qualitative component will complement the results through patients' individual interviews exploring ABPM perception and reasons for refusal, and focus groups involving general practitioners and occupational health professionals to explore perceptions and potential intervention strategies.

Perspectives: The main perspective of this study is to focus on workplace health by providing additional data on the physical repercussions of poor work-related quality of life and high perceived stress. Objectifying a confirmed medical situation could serve as a lever for identifying mental health issues. It would enable interventions to improve work-related quality of life by addressing health determinants and psychosocial risks. Various interventions could be considered through a multidisciplinary approach in the workplace, involving occupational physicians, occupational psychologists, and employers. This study could also offer insights into patient profiles at higher cardiovascular risk, help develop recommendations for screening masked hypertension, and evaluate the role of blood pressure measurements at the workplace.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients aged 40 to 65 years

Consulting one of the participating general practitioners,

Actively working

Without cardiovascular history or antihypertensive treatment

Disqualifiers

None

Trial population

Primary care working patients in primary cardiovascular prevention

Trial design

Design model

Cohort

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

316 Participants
are grouped into 1 trial group
Group A: Workers from 40 to 65 years, in primary cardiovascular prevention, consulting at general practice

Trial outcomes

Primary outcomes

1

Prevalence of masked hypertension

Normal office blood pressure (BP \<140/90 mmHg) AND 24-hour ambulatory blood pressure hypertension (daytime BP ≥135/85 mmHg OR nighttime BP ≥120/70 mmHg)

Time frame
24-hour ambulatory blood pressure monitoring recording
2

Prevalence of white-coat hypertension

High office blood pressure (BP ≥140/90 mmHg) AND normal 24-hour ambulatory blood pressure (daytime BP \<135/85 mmHg AND nighttime BP \<120/70 mmHg)

Time frame
24-hour ambulatory blood pressure monitoring recording

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Burgundy

Lead sponsor

Pôle Fédératif de Recherche et de Formation en Santé Publique Bourgogne-Franche-Comté

Collaborator

Laboratoire Psy-DREPI (UR 7458) - Université Bourgogne Europe

Collaborator

Département de Médecine Générale de Dijon (DMG) - Université Bourgogne Europe

Collaborator