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Effect of hegu point Acupressure on intensity of pain due of Phlebotomy

Effect of hegu point Acupressure on intensity of pain due of Phlebotomy in children with thalassemia Kerman Medical Center Samen Al hojaj.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014071717941N3
Enrollment
86
Registered
2014-10-26
Start date
2014-09-06
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pain. Pain, unspecified

Interventions

Intervention 1: In the experimental group, With the thumb angle to the face fines , Hegu pressure point for about 5 minutes before entering penetrating IV between the thumb and fingers of the hand tha
Rehabilitation
Treatment - Drugs
In the experimental group, With the thumb angle to the face fines , Hegu pressure point for about 5 minutes before entering penetrating IV between the thumb and fingers of the hand that venipuncture d
In the control group, did not intervene, and vienpuncture the usual method was to do section.

Sponsors

Kerman University Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: This clinical trial study is of single -blind and two-group type, which with aim research effect of hegu point Acupressure on severity of venipuncture pain. Inclusion criteria included Thalassemic children aged 6-12 and patient’s willingness to participate in the study; However, children with physical problems (verbal, mental, visual and auditory); medication to reduce pain for up to 8 hours prior to venipuncture; penetration of more than one catheter into the skin,; prolonged duration of catheter insertion (over a minute) were excluded from the study. The study population was all school-age children referring to Kerman Samenolhojaj Medical Center. 86 children were selected using stratified random sampling method; they were placed into two experimental (hegu point Acupressure For 5 minutes) and control groups (No intervention was done). Data was collected using a questionairer about the child's demographic information and Flacc behavioral pain scale.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: The beginning of the study. Method of measurement: Flacc behavioral pain scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Rostami

Kerman University of Medical Science

maryam_rostami1751@yahoo.commaryam.rostami1751@gmail.com+98 71 4254 2425

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026