- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04932681
Use of Medicinal Plants and Other Alternative and Complementary Medicines by Patients With Cancer in Reunion Island (CAMUCRI)
Evaluation of the Use of Medicinal Plants and Other Alternative and Complementary Medicines by Patients With Cancer in Reunion Island
Exploratory, observational and cross-sectional study with the aim of describing the use of plants for medicinal purposes (and other Complementary and Alternative Medicine) and identifying the determinants of this use. The methodology envisaged is mixed with an exploratory design combining qualitative (interviews) and quantitative techniques (questionnaires).
To knowledge of investigators, no study has been carried out in Reunion Island on the use of plants and other alternative and complementary medicines among cancer patients.
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Florent DRAPEAU, PharmD
- Phone Number: 02 62 35 90 00
- Email: florent.drapeau@chu-reunion.fr
Study Contact Backup
- Name: Laetitia BERLY
- Phone Number: 02 62 90 62 86
- Email: laetitia.berly@chu-reunion.fr
Study Locations
-
-
-
Saint-Denis, Réunion, 97400
- Recruiting
- CHU La Réunion
-
Contact:
- Florent DRAPEAU, PharmD
- Phone Number: 02 62 35 90 00
- Email: florent.drapeau@chu-reunion.fr
-
Principal Investigator:
- Patricia ZUNIC, MD
-
Sainte-Clotilde, Réunion, 97490
- Not yet recruiting
- Clinique Saint Clotilde
-
Contact:
- Antoine MORICEAU, PharmD
- Email: antoine.moriceau@clinifutur.net
-
Principal Investigator:
- Gilles BAUMONT, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Living in Reunion Island
- Suffering from cancer (solid tumors, hematological malignancies)
- Able to answer a questionnaire
- Patient who does not oppose to the research
Exclusion Criteria:
- Person of legal age under guardianship or under legal protection
- Persons who do not understand French or Reunionese Creole
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Qualitative group
Interview about the use of Complementary and Alternative Medecine
|
|
Quantitative group
Questionnaire about the use of Complementary and Alternative Medecine
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Use of herbal medicine
Time Frame: Day 1
|
Proportion of patients using herbal medicine (from the patient's perspective) among cancer patients.
|
Day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Barriers of dialogue between patient and practionner
Time Frame: Day 1
|
Interviews between patient and interviewer will help to extract the barriers limiting patient/practitioner dialogue on Complementary and Alternative Medicine use from patient and practitioner perspectives
|
Day 1
|
|
Need for Information on Complementary and Alternative Medicine
Time Frame: Day 1
|
Interviews between patient and interviewer will help to find out expectations about the need for information on Complementary and Alternative Medicine use from the patient's perspective and from the practitioner's perspective
|
Day 1
|
|
Improving questionnaire after the practionners' focus group
Time Frame: Day 1
|
A practionners' focus group will be organised after the interviews to review the feedbacks and opinions on the questionnaire to improve the questionnaire for the quantitative part of the study
|
Day 1
|
Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2021/CHU/05
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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