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Clinical Trials in France / NCT06538220
Recruiting Not applicable

Evaluation of the Care Pathway Offered by the "Chronic Disease Unit" to Obese Patients

NCT06538220 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2024-10-16
Last updated
2026-07-07

Condition(s) studied

Obesity

Investigational drug(s) / intervention(s)

Questionnaires and focus group

Questionnaires and focus group: To evaluate the Chronic Disease Unit care pathway, patients will respond to questionnaires : quality of life (SF-12), personal efficacy scale (GSES), "Specific self Efficacy related to Weight Management" (SEWM), Rosenberg self-esteem, body image satisfaction (QIC), state of anxiety and depression (HAD), Chronic Disease Unit satisfaction. Some patients will also participate to focus group.

Study summary

Obesity is a chronic and progressive disease medically defined as an increase in body fat, with consequences for physical, psychological and social well-being. With an estimated prevalence of 17% in France, obesity and its management remain a major public health issue. Projections by the World Health Organisation (WHO) show that the prevalence of non-communicable diseases, including obesity, is set to rise again by 2030 in all European countries.

To support patients and prevent obesity development, the French National Authority for Health (HAS) advocates change in practices and places patient education at the heart of care. The management of chronic diseases such as obesity must be offered on a long-term basis, adapting to complications onset, and patients must become active players in their treatment and the proposed care pathway. However, our experience shows that patients have difficulty finding their way around a care pathway and identifying the medical or paramedical resources that could help them to set their health goals and initiate change.

That's why the Var region has developed the "Chronic Disease Unit", which offers coordinated, adapted and individualised care pathways for patients suffering from chronic illnesses, including obesity; therapeutic education and the psychosocial dimension are at the heart of the Chronic Disease Unit approach. Depending on their psychosocial skills, each patient will be encouraged to develop skills at their own pace, but also to become autonomous in managing their illness and taking part in the healthcare decisions about them. To be autonomous, a patient must not only know what to do, but also feel able to do it, i.e. develop a sense of self-efficacy. When they have the necessary skills and believe in their abilities, patients are more likely to adopt health-promoting behaviours. While obesity generally seems to be linked to a low self-efficacy, the self-efficacy appears to be involved in weight management quality, commitment to a programme and the weight loss extent that results.

The aim of EVAMMACH study is to evaluate if the Chronic Disease Unit care pathway could promote obese patients' sense of self-efficacy and meet their expectations.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Patient identified by the network or referred by a healthcare professional, 2. Patient aged 18 or over, 3. Patient suffering from obesity defined by a BMI ≥ 30, 4. Patient who understands and speaks French. Exclusion Criteria: 1. Opposition of the patient to participation in the study, 2. Pregnant, parturient or breast-feeding woman, 3. Patient undergoing bariatric surgery, 4. Patient under judicial protection (guardianship, curatorship, etc.) or safeguard of justice, 5. Patients with unstable psychiatric disorders, 6. Patients on neuroleptics, 7. Any other reason which in the opinion of the investigator, could interfere with the evaluation of the study objectives.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
MMC La Garde Var Recruiting

More Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer trials in France

Other trials for the same condition

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 NCT06538220 on ClinicalTrials.gov ↗ ← All trials in France