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Clinical Trials in France / NCT06626061
Enrolling by invitation Not applicable

Evaluation of the CBSM Program Online and in Person to Reduce Caregiver Burnout

NCT06626061 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2025-05-01
Last updated
2025-04-11

Condition(s) studied

Burnout, Caregiver

Investigational drug(s) / intervention(s)

Cognitive Behavioral Stress management in in person group FormatCognitive Behavioral Stress management Hybrid Format

Cognitive Behavioral Stress management in in person group Format: The CBSM sessions will be delivered to participants in groups of ten, totaling eight sessions, each focused on a specific theme related to stress management. All participants will attend the complete sessions in person.

Cognitive Behavioral Stress management Hybrid Format: The CBSM (hybrid) sessions will be offered to participants online, including a total of eight video modules, each dedicated to a specific theme related to stress management. Participants will also have access to three interactive virtual sessions, summary sheets in PDF format, and audio recordings for relaxation.

Study summary

Professional burnout is a common syndrome among healthcare workers, impacting both their well-being and the quality of care provided . It is characterized by emotional exhaustion, depersonalization, and a reduced sense of personal accomplishment.

This multicenter study evaluates the effectiveness of the Cognitive Behavioral Stress Management (CBSM) program in preventing burnout. This intervention, based on cognitive-behavioral techniques, integrates stress management tools and relaxation exercises over eight 2-hour sessions. The study aims to recruit 200 healthcare workers, divided into three groups: in-person intervention, hybrid format (videos + videoconferences), and delayed intervention (in-person/hybrid), across two hospital centers (CHUGA and CHMS). Data will be collected at three time points (M0, M3, M6), with emotional exhaustion (MBI) as the primary outcome, supplemented by measures of individual, relational, and organizational factors.

By comparing different intervention modalities (in-person vs. hybrid, immediate vs. delayed), this research will provide practical recommendations to enhance burnout prevention strategies in the hospital setting.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
Accepted
Inclusion criteria : * Be a healthcare professional. * Be a volunteer. * Work at CHUGA or CHMS. * Be available to attend program sessions (in-person or hybrid). Exclusion criteria: * Protected persons (articles L1121-5 to L1121-8 of the Public Health Code), except for pregnant women for whom a benefit is expected in relation to a foreseeable minor risk for the pregnant woman or the unborn child. * Students in health-related fields. * Individuals with difficulties in understanding the French language.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Centre Hospitalier Métropole Savoie (CHMS) Chambéry France
Centre hospitalier Grenoble Alpes (CHUGA) Grenoble France

More University Hospital, Grenoble trials in France

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06626061 on ClinicalTrials.gov ↗ ← All trials in France