cancer. Malignant neoplasms,Malignant neoplasms of ill-defined, secondary and unspecified sites
Conditions
Interventions
Intervention 1: Intervention group: the intervention group on the 3-point acupressure true will done for 1 min and only one time during chemotherapy and one time after completed chemotherapy. Interv
Intervention group: the intervention group on the 3-point acupressure true will done for 1 min and only one time during chemotherapy and one time after completed chemotherapy
Placebo: in the placebo acupressure points on 3-point lies close to true for 1 minute, once during and once after completing of chemotherapy
Control group: The control group will receive routine care of patients.
Sponsors
Vice Chancellor for Research and Technology, Guilan University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: inclusion criteria: consciousness? lack of amputation? II, III, and IV stages of cancer? Chemotherapy at least in the past month ? lack of ulcer at the acupoints ? complaint of fatigue ( moderate to high) ? Having hemoglobin less than mg / dl12
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fatigue. Timepoint: Before the intervention,After intervention during chemotherapyAfter the intervention after chemotherapy. Method of measurement: Fatigue Inventory(FSS). | — |
Secondary
| Measure | Time frame |
|---|---|
| No. Timepoint: no. Method of measurement: no. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAtefeh Ghanbari
Guilan University of Medical Sciences
Outcome results
None listed