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Integrative Medicine clinical trials

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NCT ID: NCT05833165 Recruiting - Cancer Clinical Trials

Feasibility of Integrating Homeopathic Approach in a Comprehensive Cancer Center

Start date: January 1, 2023
Phase:
Study type: Observational

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.

NCT ID: NCT04692597 Recruiting - Osteoarthritis Clinical Trials

Low Level Laser Therapy (LLLT) for the Treatment of Hand Osteoarthritis.

Start date: March 2, 2021
Phase: N/A
Study type: Interventional

This study is a randomized, control trial of Active Duty and DoD Beneficiaries, age 18 years or older, with complaints of hand osteoarthritis. Subjects will be randomized into one of two groups receiving either LLLT or sham LLLT. Subjects will receive LLLT or sham LLLT weekly over a period of six weeks. At each visit, patients will rate their pain using the Defense and Veterans Pain Rating Scale (DVPRS) and assess their functionality using the Disabilities of the Arm, Shoulder, and Hand (DASH) questionnaire. Subjects will have a follow up visit six weeks after the treatment protocol for a final assessment of pain and function. The Phoenix Thera-Lase laser is a Class II, 510k cleared device (#K151521) and is legally marketed in the US. Investigators are using in accordance with its approved labeling and no changes to the approved labeling are being sought.

NCT ID: NCT03140345 Recruiting - Renal Dialysis Clinical Trials

Integrative HD Vascular Access Assessment

Start date: June 7, 2017
Phase: N/A
Study type: Observational

The aim of this two-year study is to explore the relationship among function of HVA, nail-fold capillaries and TCM constitutions based on hybridizing data mining techniques. This study will not only improve our understanding on the expressions of function of HVA, nailfold capillaries and tendency of TCM patterns, but also demonstrate the fundamental knowledge of a novel healthcare model on hemodialysis vascular access.