Clinical trial Recruiting at 1 site Observational Ages 18 and up

Integrating homeopathic care into a comprehensive cancer center

Official title: Feasibility of Integrating Homeopathic Approach in a Comprehensive Cancer Center

Run by Rambam Health Care Campus · NCT05833165 · Data updated 2026-11-12

This project will try offering homeopathic consultations to adult cancer patients at Rambam to see if patients accept and can use this approach as part of supportive care.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment250 (estimated)
SponsorRambam Health Care Campus
Academic / other
Locations1 site (Haifa)
StatusRecruiting
StartedJanuary 1, 2023
Main results expectedJanuary 1, 2028
Study endsJanuary 1, 2028
Registry record updatedAugust 7, 2025
Trial IDNCT05833165 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) treated in the Division of Oncology at Rambam who read and understand Hebrew, have ECOG performance status 0–2, and consent to participate are ideal candidates.

Probably not a fit

Patients with active psychosis, severe cognitive impairment, frailty or ECOG >2, or other unstable acute medical conditions are unlikely to benefit or be eligible to participate.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an observational feasibility project at Rambam Health Campus that offers homeopathic consultations within the existing complementary and integrative oncology service. Adult oncology patients who meet eligibility criteria will be invited to a detailed homeopathic interview and follow-up, and investigators will record uptake, reasons for choosing the service, completion of visits, and any logistical barriers. The study will collect basic patient-reported information about experience and tolerability but does not test clinical efficacy. Results will focus on acceptability, integration challenges, and practical implementation metrics to inform future work.

Why it matters

Potential benefit: If successful, it could provide an additional supportive care option that some patients find helpful for well‑being and symptom coping.

How similar studies have gone: While integrative oncology services commonly include homeopathy in some countries, high‑quality evidence of clinical benefit in cancer patients is limited, so feasibility work like this remains relatively novel in the Israeli comprehensive cancer center setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* • 18 years of age or older

  * Ability to read, write, and understand the Hebrew language
  * Patients treated at the Division of Oncology in Rambam Health Campus.
  * Performance status of ECOG 0-2.
  * Consent to participate in the study.

Exclusion Criteria:

* • Inability to understand the intent of the study and follow the instructions

  * Diagnosis of active psychosis, altered mental state or severe cognitive impairment confirmed by the patient's attending physician.
  * Frailty, ECOG worse than 2, or other unstable medical conditions as confirmed by the patient's attending physician including acute illness, fever, unclear rash or medical conditions that would preclude participation in an interview session lasting 15-30 minutes

Where it's running

  • Rambam Medical Center
    Haifa, Israel
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.