- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06515249
Integrative Therapies in Multiple Myeloma
Effectiveness and Safety of Integrative Therapies in Multiple Myeloma
Multiple myeloma is a hematologic malignancy that can cause anemia, renal failure, bone disease, and hypercalcemia. Today, myeloma is considered a chronic disease and most patients will receive ongoing biological treatments. As a result, this disease causes a number of symptoms related to the disease itself or its treatment, which include, among others, weakness and fatigue, bone or nerve pain, depression and anxiety, gastrointestinal symptoms, impairment of sexual function, etc. These symptoms cause significant damage to quality-of-life which is similar in patients who receive different treatment lines. As a result, the FDA emphasized quality-of-life as a key outcome for the approval of new drugs for the disease.
The conventional therapeutic approach to the various symptoms is based on supportive care guidelines including pharmacological and non-pharmacological treatment of pain, gastrointestinal symptoms, psychological components, etc. These treatments involve side effects and usually refer to individual symptoms.
Complementary and integrative medicine includes treatments of touch, movement, mind-body, acupuncture, nutrition and nutritional supplements. Many studies have shown the effectiveness of these treatments on various symptoms in cancer patients including pain, depression and anxiety, fatigue and weakness, gastrointestinal symptoms, etc. In myeloma patients, the effect of diet and nutritional supplements was mainly examined, but there is also little information on the effectiveness of mind-body treatments on symptoms of anxiety and depression, as well as acupuncture on neuropathy or on symptoms experienced by myeloma patients around autologous bone marrow transplantation.
In recent years, a wide variety of new drugs have entered the market that cause side effects that were unknown until now and little is known about the effect of complementary medicine treatments on symptoms and quality-of-life of myeloma patients since the development of these drugs.
In this study we will examine the effect of complementary and integrative medicine treatments (including acupuncture, touch, movement, mind-body) on the quality-of-life and symptoms that characterize myeloma patients during treatment with different lines of therapy, including new drugs.
Patients with a diagnosis of multiple myeloma who meet the study's inclusion criteria will be divided into the intervention group (complementary medicine treatments) and the control group (no treatments) according to their preferences. All the patients of the intervention group and the patients of the control group who agree will be asked to fill out quality-of-life questionnaires validated and translated into Hebrew, Arabic and Russian before the start of the treatment. The questionnaires include European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) which is a general quality-of-life questionnaire for cancer patients, with the addition of MY20 which is an addition of 20 specific questions for patients with multiple myeloma, the Edmonton Symptom Assessment System (ESAS) questionnaire which examines the severity of 10 common symptoms in patients with malignant disease, and the EuroQol-5 Dimension (EQ-5D) questionnaire which examines quality-of-life in cancer patients and is used as a primary outcome in many clinical studies. The same questionnaires will be sent again 1-2 weeks after the end of the treatments in the intervention group and 6-8 weeks after recruitment in the control group. Socio-demographic and medical data will also be collected from the patients and their medical records.
Study Overview
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Ilana Levy Yurkovski, MD
- Phone Number: +972525086128
- Email: ilana.levy@b-zion.org.il
Study Locations
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Haifa, Israel, 3339419
- Recruiting
- Bnai Zion Medical Center
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Contact:
- Miriam Goldberg
- Phone Number: 972-48359351
- Email: miriam.goldberg@b-zion.org.il
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Principal Investigator:
- Ilana Levy Yurkovski, MD
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Sub-Investigator:
- Ohad Cohen-Naznin
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age over 18
- Diagnosis of multiple myeloma
- Possibility to answer questionnaires once a month in Hebrew, Arabic or Russian
- Signing an informed consent form
Exclusion Criteria:
- Age under 18 years
- In patients who will receive acupuncture: platelet level below 20x10^9/L
- In patients who will receive reflexology: deep vein thrombosis in the leg
- Hemodynamic instability
- Psychiatric disorder impairing competence
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: Control
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Experimental: Integrative medicine
Integrative medicine treatments including acupuncture, touch, movement, mind-body, as patient's and staff's choice
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Integrative medicine treatments including acupuncture, touch, movement, mind-body, as patient's and staff's choice
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Quality-of-life specific to myeloma patients
Time Frame: From enrollment to 2 weeks after end of treatment in intervention group and 8 weeks after enrollment in control group
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EORTC QLQ-MY2 (European Organization for the Research and Treatment of Cancer Quality of Life for Myeloma patients) score at 1-2 weeks after end-of-treatment in intervention group and 7-8 weeks after recruitment in control group.
It comprises 20 questions that address four myeloma-specific HRQoL domains: Disease Symptoms, Side Effects of Treatment, Future Perspective, and Body Image.
Domain scores are averaged and transformed linearly to a score ranging from 0-100.
A high score for Disease Symptoms and Side Effects of Treatment represents a high level of symptomatology or problems, whereas a high score for Future Perspective and Body Image represents better outcomes.
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From enrollment to 2 weeks after end of treatment in intervention group and 8 weeks after enrollment in control group
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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General quality-of-life evaluation
Time Frame: From enrollment to 2 weeks after end of treatment in intervention group and 8 weeks after enrollment in control group
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European Organization Research for Treatment of cancer core quality of life (EORTC-QLQ-C30) questionnaire summary score which is calculated from the mean of 13 of the 15 quality-of-life (QLQ-C30) scales of the questionnaire = (Physical Functioning+ Role Functioning+ Social Functioning+ Emotional Functioning+ Cognitive Functioning+ 100-Fatigue+ 100-Pain+ 100-Nausea_Vomiting+ 100-Dyspnoea+ 100-Sleeping Disturbances+ 100-Appetite Loss+ 100-Constipation+ 100-Diarrhoea)/13.
Scores range from minimum 0 to maximum 100; a higher score represents a higher ("better") level of functioning, or a higher ("worse") level of symptoms.
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From enrollment to 2 weeks after end of treatment in intervention group and 8 weeks after enrollment in control group
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Symptom relief
Time Frame: From enrollment to 2 weeks after end of treatment in intervention group and 8 weeks after enrollment in control group
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Edmonton Symptom Assessment System (ESAS): assesses the severity over time of nine symptoms common among patients with cancer and other advanced illness: pain, tiredness, drowsiness, nausea, shortness of breath, appetite, depression, anxiety, and wellbeing.
A higher score represents a higher ("worse") level of symptoms.
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From enrollment to 2 weeks after end of treatment in intervention group and 8 weeks after enrollment in control group
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Compliance to conventional therapy
Time Frame: From enrollment to 1 year after enrollment
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Relative dose intensity (RDI) which is the ratio of delivered dose intensity (DDI) of myeloma treatment with standard dose intensity (SDI) of myeloma treatment = DDI/SDI
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From enrollment to 1 year after enrollment
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Economic analysis
Time Frame: From enrollment to 3 months after enrollment
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Calculation of quality-adjusted life years based on EuroQol-5 Dimension (EQ-5D) scale.
The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression.
Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems.
The patient indicates health state by ticking the box next to the most appropriate statement in each of the five dimensions.
This decision results in a 1-digit number that expresses the level selected for that dimension.
The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state.
The EQ visual analogue scale (VAS) records the patient's self-rated health on a vertical visual analogue scale, where the endpoints are labelled 'The best health you can imagine' and 'The worst health you can imagine'.
The VAS can be used as a quantitative measure of health outcome that reflect the patient's own judgement.
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From enrollment to 3 months after enrollment
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Overall response rate (ORR) to myeloma treatment
Time Frame: From enrollment to 1 year after enrollment
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Percentage of patients who have a partial response or complete response to the treatment of myeloma
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From enrollment to 1 year after enrollment
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Progression-free survival (PFS)
Time Frame: From enrollment to 2 years after enrollment
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The length of time during and after the treatment of myeloma that patient lives and disease does not progress
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From enrollment to 2 years after enrollment
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Overall survival (OS)
Time Frame: From enrollment to 2 years after enrollment
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The length of time during and after the treatment of myeloma that patient lives
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From enrollment to 2 years after enrollment
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ilana Levy Yurkovski, MD, Bnai Zion Medical Center, Haifa, Israel
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Cardiovascular Diseases
- Vascular Diseases
- Immune System Diseases
- Neoplasms by Histologic Type
- Neoplasms
- Lymphoproliferative Disorders
- Immunoproliferative Disorders
- Hematologic Diseases
- Hemorrhagic Disorders
- Hemostatic Disorders
- Paraproteinemias
- Blood Protein Disorders
- Multiple Myeloma
- Neoplasms, Plasma Cell
Other Study ID Numbers
- 0054-24-BNZ
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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