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Quality of Life in Lymphoma Patients One Year Post-chemotherapy

Quality of Life in Lymphoma Patients and Cancer Care Pathway One Year Post-chemotherapy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04187118
Acronym
QUALIPSO-L
Enrollment
600
Registered
2019-12-05
Start date
2020-01-28
Completion date
2025-06-30
Last updated
2023-09-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lymphoma

Keywords

Lymphoma, Quality Of Life, Cancer Care Pathway, Post-Chemotherapy

Brief summary

Malignant lymphomas are considered as among the most chemo-sensitive cancers. ML are cured in more than 85% of patient, the majority with complete response. After this active phase of treatment, patients are in after cancer period. Toulouse University Hospital developed since 2006 the Ambulatory Medical Assistance for After Cancer program on lymphoma patient. Ambulatory Medical Assistance for After Cancer is very efficient for detecting physical and psychological complications which impact quality of life. The investigators identified 22% of lymphoma patients who had a reduced quality of life one year after the end of chemotherapy. The present study aims to investigate the evolution of observed complications and identify cancer care pathway which decrease the quality of life reduction risk in patients one year after lymphoma chemotherapy.

Detailed description

Quality of life, as well anxiety, depression, social isolation, fear of cancer recurrence, post traumatic stress, will be measured in lymphoma patients, after a first line chemotherapy. Care cancer pathway will be also evaluated. Self-administered questionnaires will be performed on website (www.hospitalidee.fr) after inclusion and 12 months after.

Interventions

OTHERQuality of life

Quality of life one year post chemo-therapy

Sponsors

Force Hémato
CollaboratorUNKNOWN
Hospitalidee
CollaboratorUNKNOWN
University Hospital, Toulouse
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients being in complete response after a first therapy for lymphoma * Malignant lymphoma (Hodgkin or non-Hodgkin) treated by anthracyclines with a minimum of 6 cycles, followed or not by autologous hematopoietic stem cell transplantation * Patients informed of the study and not opposed to the research

Exclusion criteria

* Patients under legal guardian . * Patients unavailable to formulate non-opposition to the study

Design outcomes

Primary

MeasureTime frameDescription
Quality of life change: Quality of Life-C30 French versionChange from baseline quality of life at 12 monthHealth-related quality of life is evaluated by the use of Quality of Life-C30 French version

Countries

France

Contacts

Primary ContactLoïc YSEBAERT, MD, PhD
ysebaert.loic@iuct-oncopole.fr561145940
Backup ContactFabien DESPAS, Pharm, PhD
fabien.despas@univ-tlse3.fr561145940

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026