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Clinical Trials in France / NCT06102876
Active, not recruiting Observational

Feasibility of Physical Activity in Older Adults With Haematological Malignancies: ACCES Study

NCT06102876 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2023-11-14
Last updated
2025-04-10

Condition(s) studied

GeriatricHaematologic Neoplasm

Investigational drug(s) / intervention(s)

Physical activity (PA) program

Physical activity (PA) program: The PA program is specific for each patient according to their mobility profile assessed using a decision tree comprising 3 tests: 1) the number of repetitions in the 30-second sit-to-stand test, 2) the score in the Short Physical Performance Battery (SPPB) test and 3) grip strength. The PA program has to be performed once daily.

Study summary

The aim of this study is to implement a simple and unsupervised home-based physical activity (PA) program for cancer patients in 2 oncogeriatric units in Toulouse Hospital (day hospital and week hospital).

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
inclusion criteria: * suffering from a hematological malignancy (Myelodysplasia, Leukemia of any type, Lymphoma, Myeloma) * patient affiliated to a social security insurance * Patient undergoing or scheduled chemotherapy (\< 3 months) and/or immunotherapy and/or targeted therapy. Exclusion criteria: * Life expectancy estimated at less than 3 months by the unit doctor; * Cognitive impairment (not allowing comprehension of the physical activity program and research project) defined by Mini-Mental State Examination (MMSE) \<20/30; * Patient included in a clinical trial that potentially interferes with the study objective (geriatric interventional study, early drug study, study modifying the patient's lifestyle habits).; * Acute health problem (fever, severe anemia, intense pain, etc.) limiting the possibility of involvement in the program; * Contraindication to physical activity; * Patient under legal protection (guardianship or curatorship or safeguard of justice); * Refusal of patient or primary caregiver to participate.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Chu de Toulouse Toulouse France

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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 NCT06102876 on ClinicalTrials.gov ↗ ← All trials in France