CAMUCRI: Use of Medicinal Plants and Other Alternative and Complementary Medicines by Patients With Cancer in Reunion Island

Sponsor
Centre Hospitalier Universitaire de la Réunion (Other)
Overall Status
Recruiting
CT.gov ID
NCT04932681
Collaborator
APLAMEDOM (Other)
520
2
20
260
13

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    520 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Evaluation of the Use of Medicinal Plants and Other Alternative and Complementary Medicines by Patients With Cancer in Reunion Island
    Anticipated Study Start Date :
    Apr 1, 2022
    Anticipated Primary Completion Date :
    Apr 1, 2023
    Anticipated Study Completion Date :
    Dec 1, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    Qualitative group

    Interview about the use of Complementary and Alternative Medecine

    Quantitative group

    Questionnaire about the use of Complementary and Alternative Medecine

    Outcome Measures

    Primary Outcome Measures

    1. Use of herbal medicine [Day 1]

      Proportion of patients using herbal medicine (from the patient's perspective) among cancer patients.

    Secondary Outcome Measures

    1. Barriers of dialogue between patient and practionner [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

    2. Need for Information on Complementary and Alternative Medicine [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

    3. Improving questionnaire after the practionners' focus group [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

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 CHU La Réunion Saint-Denis Réunion 97400
    2 Clinique Saint Clotilde Sainte-Clotilde Réunion 97490

    Sponsors and Collaborators

    • Centre Hospitalier Universitaire de la Réunion
    • APLAMEDOM

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Centre Hospitalier Universitaire de la Réunion
    ClinicalTrials.gov Identifier:
    NCT04932681
    Other Study ID Numbers:
    • 2021/CHU/05
    First Posted:
    Jun 21, 2021
    Last Update Posted:
    Apr 8, 2022
    Last Verified:
    Mar 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Apr 8, 2022