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Property:Inclusion criteria

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V
Patients with carcinomas in the floor of the mouth, who underwent preoperative radiotherapy  +
Histologically confirmed diagnosis of cancer, at least 18 years of age, oxaliplatin chemotherapy, and adequate hematologic parameters to allow chemotherapy  +
W
Patients with newly diagnosed head and neck squamous cell carcinoma who were being scheduled for surgery  +
Patients with untreated inoperable bronchopulmonary carcinomas of various entities  +
21 years or older; having a diagnosis of stage III or IV breast cancer, metastasis, or recurrence; being able to perform basic activities of daily living; being cognitively intact and without a documented diagnosis of mental illness; being able to speak and understand English; having access to a telephone; being able to hear normal conversation; receiving chemotherapy at intake into the study; and having a score of 11 or lower on the Palliative Prognostic Score (Pirovano et al., 1999), which indicates a 30% probability of having a life expectancy of at least three months  +
Patient inclusion criteria were: 1) age >21, 2) stage III or IV breast cancer, 3) able to perform basic activities of daily living, 4) undergoing chemotherapy, targeted or hormonal therapy at the time of enrollment, 5) able to speak and understand English, 6) having access to a telephone, 7) able to hear normal conversation, and 8) cognitively oriented to time, place, and person (determined via recruiter). Friend/family caregiver inclusion criteria were 1) age >18, 2) able and willing to provide at least one 30-minute protocol session per week for four consecutive weeks, 3) able to speak and understand English, 4) access to a telephone, 5) able to hearnormal conversation, and 6) cognitively oriented to time, place, and person (determined via recruiter).  +
Y
Patients scheduled to receive single-agent capecitabine chemotherapy for breast, colorectal, and other cancers  +
Patients with histologic diagnosis of breast cancer, history of receiving at least one chemotherapy injection, receiving single-day cycles of chemotherapy (each cycle separated from next by ≥ 2 weeks); experiencing vomiting in previous sessions, and having normal values of hematologic and biomedical laboratory parameters.  +
Z
Cancer patients receiving anthracycline chemotherapy in their protocol alone (without any cardioprotective agent), aged 20-60 years  +
Patients who were scheduled to have a single-day chemotherapy regime and to receive a 5-HT3 receptor antagonist antiemetic and/or the antiemetic aprepitant. Patients with histologically confirmed diagnosis of cancer currently being treated with chemotherapy. Patients must also have received at least one previous chemotherapy treatment with the same chemotherapeutic agent and have experienced nausea or vomiting of any severity as a result of that treatment.  +
Ö
Being older than 18, knowing the diagnosis of the disease, receiving no radiotherapy, receiving an epirubicin and cyclophosphamide, having received no reflexology therapy before, literate in Turkish, having no hemorrhage, epilepsy, or fever, having no paraplegia or thrombosis, having no gall-kidney stones, having no leg varicosis and foot disease (open wound or fracture on foot), having no diagnosis of psychiatric disorder or dementia, having accepted to participate in the study.  +
Being older than 18, knowing the diagnosis of the disease, receiving no radiotherapy, receiving a epirubicin and cyclophosphamide, having received no reflexology therapy before, being literate in Turkish  +