At a glance
ClinicalIndex Comparison Record- ✓Diagnosis of breast cancer
- ✓Scheduled to receive chemotherapy containing doxorubicin (any dose) without concurrent radiotherapy or interferon
- ✓Age 18 years or older
- ✓Chemotherapy naïve
- ✕Clinical evidence of lymphedema, current bowel obstruction, or symptomatic brain metastases
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Acupressure and Relaxation for Nausea Control
In Brief
A Phase 2 clinical trial evaluating Acupressure expectancy enhancement for Nausea. Completed, enrolled 83 participants across 1 site.
Detailed Summary
This study hypothesizes that patients receiving efficacy enhancing information about the acupressure bands will expect less treatment-related nausea, which will subsequently result in less treatment-related nausea compared to patients who do not receive such information. This study extends prior research by utilizing a randomized controlled trial in a clinical environment to examine the efficacy of an intervention that is specifically designed to reduce patients' response expectancies concerning nausea development from cancer treatments, and, thereby, reduce nausea. The objectives of this study are as follow: 1. To provide preliminary data on whether a two-tiered strategy to increase patients' expectancies for nausea prevention and/or management will result in reduced chemotherapy-induced nausea. 2. To provide preliminary data on whether a two-tiered strategy to increase patients' expectancies for nausea prevention and/or management will result in increased health-related quality of life (HRQL) in patients receiving emetogenic chemotherapy. To provide preliminary data on whether a two-tiered strategy to increase patients' expectancies for nausea prevention and/or management is more effective than a single-tiered strategy in reducing chemotherapy- induced nausea.
Study Details
Timeline
Interventions
This study hypothesizes that patients receiving efficacy enhancing information about the acupressure bands will expect less treatment-related nausea, which will subsequently result in less treatment-related nausea compared to patients who do not receive such information. This study extends prior research by utilizing a randomized controlled trial in a clinical environment to examine the efficacy of an intervention that is specifically designed to reduce patients' response expectancies concerning nausea development from cancer treatments, and, thereby, reduce nausea.