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Effect of the P6 Acupressure on the amount of anxiety and the intensity of the pain caused by the venipuncture in patients with Thalassemia

Not Applicable
Recruiting
Conditions
Patients with thalassemia.
Beta thalassemia
D56.1
Registration Number
IRCT20200109046066N1
Lead Sponsor
Yasouj University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
80
Inclusion Criteria

Ability to communicate and answer questions
Consent to participate in the study and sign the informed consent form

Exclusion Criteria

Patient's dissatisfaction with the study
Failure of venipuncture or need to be reunited
taking analgesics within 3 hours before or during the study
Receive another painful intervention while the angiocut is embedded
Use of hypnotic, anxiolytic and antidepressant drugs before intervention

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Anxiety score in Spiegel Berger questionnaire. Timepoint: Anxiety levels before and after the intervention. Method of measurement: Spielberger’s State-Trait Anxiety Inventory (STAI).;Pain score based on visual analogue scale(VAS). Timepoint: Severity of pain during and after the intervention. Method of measurement: Visual Analogue Scale(VAS).
Secondary Outcome Measures
NameTimeMethod
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