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The Effect of Two Methods of Distraction and Acupressure on Pain and Anxiety

Not Applicable
Conditions
..
Registration Number
IRCT20100823004617N14
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Children aged 12-6 admitted in the oncology department
Full conscious to place, time and person
The ability to communicate verbally
Having a previous experience of peripheral intravenous cannulation
Acquiring informed consent of the child and parents
The health of the eyes and the hearing

Exclusion Criteria

Use of pain relief medications 8 hours prior to peripheral intravenous cannulation
More than one catheter entry into the skin
The location of the Hugo Point has a previous injury and pain.
Perform a painful procedure on the baby within 8 hours of the baby's stroke

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain caused by peripheral intravenous cannulation. Timepoint: Before the intervention and after the intervention. Method of measurement: VAS tool.;Anxiety caused by peripheral intravenous cannulation. Timepoint: Before the intervention and after the intervention. Method of measurement: FAS tool.
Secondary Outcome Measures
NameTimeMethod
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