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

Recruiting

Conditions

Study Type

Observational

Enrollment (Anticipated)

520

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Saint-Denis, Réunion, 97400
        • Recruiting
        • CHU La Réunion
        • Contact:
        • Principal Investigator:
          • Patricia ZUNIC, MD
      • Sainte-Clotilde, Réunion, 97490
        • Not yet recruiting
        • Clinique Saint Clotilde
        • Contact:
        • Principal Investigator:
          • Gilles BAUMONT, MD

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

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients with cancer linving in the Reunion Island

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

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

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

This is where you will find people and organizations involved with this 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 (Anticipated)

April 1, 2022

Primary Completion (Anticipated)

April 1, 2023

Study Completion (Anticipated)

December 1, 2023

Study Registration Dates

First Submitted

May 18, 2021

First Submitted That Met QC Criteria

June 18, 2021

First Posted (Actual)

June 21, 2021

Study Record Updates

Last Update Posted (Actual)

April 8, 2022

Last Update Submitted That Met QC Criteria

March 31, 2022

Last Verified

March 1, 2022

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)?

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.

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