About this trial
This clinicaI trial is being done to determine if acupressure is helpful to reduce anxiety related to chemotherapy, compared with "sham" (or placebo) acupressure in patients with cancer. Anxiety, experienced by many patients with cancer, can be related to chemotherapy and may contribute to other symptoms, such as nausea and poor quality of life. Some patients diagnosed with cancer express interest in non-medicine ways to manage symptoms. Acupressure is the application of non-invasive finger pressure along energy points throughout the body in order to relieve pain and induce a feeling of well-being. Previous research has shown that acupressure can help both adults and children with their anxiety in certain situations, such as after surgery. Patients can be taught how to do the acupressure on themselves, making this an intervention that can be done anywhere. Acupressure is well tolerated with minimal reports of adverse reactions. Undergoing acupressure may be effective in reducing anxiety in cancer patients receiving chemotherapy.
Eligibility criteria
Qualifiers
NURSE-LED INTERVENTION: Age >= 18 years and be diagnosed with cancer
NURSE-LED INTERVENTION: Undergoing systemic, antineoplastic therapy
NURSE-LED INTERVENTION: Ability to provide oral consent
NURSE-LED INTERVENTION: Willingness to undergo a nurse-led acupressure intervention
Disqualifiers
Prior experiences with acupressure, or training in acupressure points
Trial design
Treatments tested in this trial
- Acupressure Therapy
- Acupressure Therapy - placebo
- Acupressure Therapy - self-administered
- Health Promotion and Education
- Survey Administration