- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05156931
Exploration of Patient Self-medication Practices During and After Cancer in France (CASEME)
August 5, 2026 updated by: University Hospital, Clermont-Ferrand
Exploration of Patient Self-medication Practices During and After Cancer in France: Cross-sectional Observational Study With Online Response
The purpose of this study is to assess the patient self-medication practices during and after cancer in France, using an online questionnaire
Study Overview
Status
Completed
Conditions
Detailed Description
Patients will be contacted by email from patient's associations.
Patients will be informed of the objectives of the study and will be free to answer or not to the online questionnaire.
Study Type
Observational
Enrollment (Actual)
681
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Clermont-Ferrand, France
- CHU clermont-ferrand
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients contacted by cancer patient's association
Description
Inclusion Criteria:
- Past or active cancer
Exclusion Criteria:
- Speaking French
- Not living in France
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-medication
Time Frame: day 1
|
declaration of a practice of self-medication
|
day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Class of products used in self-medication
Time Frame: day 1
|
non-prescription medicine, herbal medicine, aromatherapy, homeopathy, and food supplements
|
day 1
|
|
Indication for self-medication
Time Frame: day 1
|
For treatment of side-effects, improvements in anti-cancer effects
|
day 1
|
|
Origin of self-medication products
Time Frame: day 1
|
pharmacy, market, internet, other
|
day 1
|
|
Perception of adverse effects and drug-drug interaction related to self medication
Time Frame: day 1
|
yes / no
|
day 1
|
|
QLQ-C30 questionnaire
Time Frame: day 1
|
Global health status Functional scales Physical functioning Role functioning Emotional functioning Cognitive functioning Social functioning Fatigue Nausea and vomiting Pain Dyspnoea Insomnia Appetite loss Constipation Diarrhoea Financial difficulties
|
day 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 14, 2021
Primary Completion (Actual)
April 30, 2022
Study Completion (Actual)
April 30, 2022
Study Registration Dates
First Submitted
December 1, 2021
First Submitted That Met QC Criteria
December 1, 2021
First Posted (Actual)
December 14, 2021
Study Record Updates
Last Update Posted (Actual)
August 7, 2026
Last Update Submitted That Met QC Criteria
August 5, 2026
Last Verified
August 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RNI 2021 BALAYSSAC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.