Dietary Supplements Among Cancer Patients: Tolerance, Impact on Medications, and Potential Drug Interactions

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Mohammed VI de la Recherche et de l'Innovation (CM6RI)

About this trial

The goal of this observational study is to To assess the prevalence and patterns of dietary supplement use among patients with cancer and to analyze the impact of these supplements in the context of anticancer medical treatments, including chemotherapy, targeted therapies, hormone therapy, and immunotherapies.

The main questions it aims to answer :

* What is the prevalence of dietary supplement use among cancer patients, and what is their tolerance profile? * Are there any potential drug interactions between dietary supplements and anticancer medications?

Participants will:

* Provide sociodemographic information, including age, sex, educational level, and other relevant characteristics. * Report their use of dietary supplements, including the types of supplements consumed (e.g., vitamins, minerals, herbal products), dietary practices, frequency and duration of use, and reasons for consumption (e.g., medical recommendation or self-medication). * Report any perceived adverse effects related to dietary supplement use to assess tolerance. * Allow the collection of relevant clinical data from their medical records, including cancer type, ongoing anticancer treatments, and treatment-related adverse effects.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients diagnosed with cancer and receiving medical anticancer treatment, including chemotherapy, hormone therapy, immunotherapy, and targeted therapies.

Current or recent use of one or more dietary supplements (e.g., vitamins, minerals, herbal products, or other nutritional supplements).

Adult patients : >=18

Disqualifiers

Patients unable to complete the study questionnaire because of cognitive impairment or a deteriorated health condition.

Failure or refusal to provide written informed consent.

Trial population

Adult patients diagnosed with cancer and receiving medical anticancer treatment (chemotherapy, hormone therapy, immunotherapy, or targeted therapy) at the study site. Participants will be assessed for dietary supplement use, tolerance, and potential interactions between dietary supplements and anticancer medications.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Dietary Supplement Use Assessment

    Behavioral

    Participants will complete a structured face-to-face questionnaire on dietary supplement use, reasons for Use, frequency and duration of use, perceived adverse effects, and concomitant anticancer treatments.

Treatment groups

1,000 Participants
are divided into 1 treatment group
Group A: Cancer Patients Using Dietary Supplements1 intervention

Trial outcomes

Primary outcomes

1

Prevalence of Dietary Supplement Use and Tolerance

Assessment of the prevalence of dietary supplement use among cancer patients and evaluation of adverse effects associated with dietary supplement consumption.

Time frame
At enrollment
2

Potential Drug-Supplement Interactions

Assessment of potential interactions between dietary supplements and anticancer medications

Time frame
At enrollment or single study visit

Secondary outcomes

1

Potential Drug-Supplement Interactions Assessed by Artificial Intelligence

Assessment of potential interactions between dietary supplements and anticancer treatments using Hedrine software.

Time frame
At enrollment or Single study visit

Other outcomes

Sponsors and contacts

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