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Clinical Trials in Israel / NCT05833165
Recruiting Observational

Feasibility of Integrating Homeopathic Approach in a Comprehensive Cancer Center

NCT05833165 · tracked via the Priya Life Science Israel tracker
Phase
Observational
Started
2023-01-01
Last updated
2025-08-07

Condition(s) studied

CancerQuality of LifeComplementary MedicineIntegrative Medicine

Investigational drug(s) / intervention(s)

Feasibility of a supportive approach

Feasibility of a supportive approach: Evaluating reasons for patients to use the approach

Study summary

Supportive and palliative care play an important role in cancer treatment, and when introduced early can improve quality of life and may even increase median survival rates, as shown in patients with advanced lung cancer. Complementary and integrative medicine (CIM) is a popular supportive approach among oncology patients and is on the rise worldwide. In many countries, homeopathy is being one the CIM methods integrated with a general sense that this treatment is beneficial to the well-being and quality of life (QoL) of cancer patients. In this observational study we will evaluate the feasibility of integrating homeopathic approach in patients attending the complementary and integrative oncology service at the division of oncology in Rambam Health Campus in Haifa, Israel, a major referral comprehensive cancer center.

This observational study will evaluate three main ingredients of acceptance:

* Obtaining the reasons that patients willing to integrate this supportive approach
* Patient acceptance of this supportive approach as well as compliance with the homeopathic approach
* Obtaining retrospective subjective information from the patients through validated quality of life questionnaires. (MYCaW, Distress Thermometer, and ESAS-R) Measures which are used routinely in integrative oncology encounters.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Rambam Medical Center Haifa Israel Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05833165 on ClinicalTrials.gov ↗ ← All trials in Israel