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NCT02653820 Clinical Trial

Complementary Effect of Reflexology on Chemotherapy-Induced Nausea and Vomiting

Reflexology Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT02653820
Other study ID # 102-15 HYMC
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received January 6, 2016
Last updated January 10, 2016
Start date February 2016
Est. completion date February 2018

Study information
Verified date January 2016
Source Hillel Yaffe Medical Center
Contact Katerina Shulman, MD
Phone 972-4-6188280
Email katerinas@hy.health.gov.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

Reflexology treatment may influence the severity of chemotherapy-induced nausea and vomiting. This study aims to investigate the clinical effect of reflexology on chemotherapy-induced nausea and vomiting.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 40
Est. completion date February 2018
Est. primary completion date February 2018
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Chemotherapy patients

Exclusion Criteria:

- Myocardial Infarction in previous 6 months

- Mechanical colonic obstruction

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Intervention

Other:
• Reflexology

Locations
Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)
Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change in Severity of Nausea Nausea will be assessed both before after three weeks of reflexology treatment by Common Toxicity Criteria Adverse Events Tool Three weeks No
Primary Change in Severity of Vomiting Vomiting will be assessed both before after three weeks of reflexology treatment by Common Toxicity Criteria Adverse Events Tool Three weeks No
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