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  Background and Objective: The Fatigue related to cancer is one of the common problems of both patients and care-givers. Nowadays, acupressure as a complementary medicine has become more common in patients with cancer for balancing and improving body energy. This study aimed to assess the effect of acupressure on the fatigue of patients with cancer.

  Material and Methods: This blinded- randomized clinical trial was conducted on 85 patients with cancer in hematology ward of Beheshti hospital of Hamadan. The subjects were located in three groups of intervention, sham and control. First, the fatigue level was measured by Brief Fatigue Inventory (BFI) as a baseline. Then, real acupressure in intervention group and unreal acupressure in sham group was performed for 10 days and only routine cares were given in control group. The fatigue amount was measured on the fifth and tenth days. The Data was analyzed by SPSS software version 16, using paired T- test and repeated measurements.

  

  Results: Acupressure was effective on the fatigue of patients with cancer (p<0.001). However, conducting unreal acupressure in sham group was effective as well (p<0.01), but the routine cares in control group was not effective and even in some cases led to increased fatigue.

  

  Conclusion: Acupressure can be used as a complementary therapy to decrease the fatigue in the patients with cancer considering its low cost, safety and simplicity.

 

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Background and Objective: Delivery period can be an effective factor on pregnancy outcomes and feto-maternal complications. Since its prolongation may lead to medical and surgical interventions, we aimed to determine the effect of acupressure on delivery duration of nulliparous women. 

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Background: A headache is the most common post-traumatic complaint in patients. Nurses can help to relieve the pain and to improve the quality of the care through non-pharmacological methods. The aim of this study was to determine the effect of pressure on Hugo point on the severity of a headache after head injury.
Methods: In this clinical trial, 60 patients were randomly divided into two intervention and control groups after accessible sampling. At first, the severity of a headache was measured by Visual Analogue Scale. In experimental group, the pressure was applied to Hugo point for 2 minutes followed by rest for 2 minutes; this procedure was repeated for 7 times. During this period, the control group received only routine care. The patients' pain scores were measured again after the intervention. Data analysis was performed using SPSS v.20 software.
Results: There was a significant difference between the scores of pain in the experimental group before and after the intervention (P <0.05), however, this difference was not significant in the control group.
Conclusion: Considering the ease of performing and the safety of this method, it is suggested to be used as an effective method to reduce the headache in patients.