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Clinical Trials in France / NCT05800535
Recruiting Observational

JUMP Prevalence of Sarcopenia and Chemobrain in Post-cancer Patients

NCT05800535 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-02-10
Last updated
2025-11-21

Condition(s) studied

CancerSarcopenia

Investigational drug(s) / intervention(s)

Study of the adverse effects of long-term oncological treatmentsStudy of the long-term side effects of oncological treatments on the anxiety-depressive and cognitive state of patients

Study of the adverse effects of long-term oncological treatments: Cognitive and muscular evaluation of patients who have received oncological treatments, away from the latest treatments to assess their impacts

Study of the long-term side effects of oncological treatments on the anxiety-depressive and cognitive state of patients: Cognitive and anxiety-depressive evaluation of patients who have received oncological treatments, away from the latest treatments to assess their impacts

Study summary

Therapeutic advances in oncology have transformed the prognosis of cancer patients, placing a significant number of them either in a context of recovery or in prolonged remission close to a chronic disease. Thus, the reconquest of a life after cancer becomes possible but raises many challenges for the patient, his entourage, the medical profession and our society. One of the major challenges is the detection and management of treatment side effects for all patients. In addition to the standard organic assessment (glycaemia, creatinine, liver test, blood count), we are mainly interested in muscle deconditioning and cognitive impairment, which are particularly disturbed in these populations. After the evaluation day, patients are referred to the most appropriate structures (Adapted physical activity, sports for health, and rehabilitation at Henry Gabriel Hospital).

JUMP research is part of axis 2 of the 2021-2030 cancer plan: "Limiting sequelae and improving quality of life", through sheets 1 (research) / 6 (access and quality) / 7 (prevention). This leads to the concrete implementation on the territory of adapted care channels in the city: medical structure, physiotherapy, Adapted Physical Activity (APA) structures, associative structures; which makes it possible to develop and strengthen the city-hospital link. Finally, it allows the patient to take ownership and get involved in the project, allowing in the future to make them truly active in they care and to advise and motivate their peers.

This study is non-interventional, it uses research on data that is already collected as part of conventional care, during the JUMP evaluation day.

This study allows the investigators to constitute a cohort of patients to study different parameters related to the disease or to the treatments received.

Our main objective in this study is to describe the muscular and neurocognitive impairment of post-cancer patients evaluated as part of the JUMP program.

Eligibility

Sex
ALL
Min age
18 Years
Max age
74 Years
Healthy volunteers
No
Inclusion Criteria: * Age : 18 to 74 years * localization of the primitive: breast, lung, melanoma, testicle, bladder, kidney, ovary, colon and pancreas, hemopathy * patient who benefited from the post-cancer assessment day- Exclusion Criteria: * Under 18years * Over 74 years * Patient who did not received any chemical treatment * Patient who do not wish to participate

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Service de Rhumatologie, Hospices Civils de Lyon, Groupement Hospitalier Lyon Sud Pierre-Bénite France Recruiting

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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 NCT05800535 on ClinicalTrials.gov ↗ ← All trials in France