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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05411289
Other study ID # P.T.REC/012/003704
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 7, 2022
Est. completion date July 15, 2022

Study information

Verified date November 2022
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the effect of acupressure on labor pain and anxiety levels during labor in primiparas women


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date July 15, 2022
Est. primary completion date July 8, 2022
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 30 Years
Eligibility Inclusion Criteria: - Primiparas women aged from 20 to 30 years old, - gestational age of between 37 and 40 weeks according to ultrasonography. - A fetal weight of between 2500 and 3500 g according to ultrasonography or clinical examination . - They are transferred to labor room if active labor is in progress (defined as cervical dilatation 3 cm and the presence of regular uterine contraction, - having a single and healthy fetus in the vertex position Exclusion Criteria: - who were needing an emergency C-section. - Women having a current or previous high-risk pregnancy - who have experienced pregnancy complications - Women with a systemic disease during pregnancy . Women with a psychological disorder

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
acupressure
Pressures were applied on three points consecutively, firstly on two points bilaterally Hugo point (LI4) and He-7 (Shenmen), then pressure was applied on sanyinjiao (SP6). pressure was applied gradually for 30 seconds on the above mentioned points. Then this pressure was slowly intensified to the extent that the patient felt tingling, numbness, heaviness, and strain in the surrounding area.
sham acupressure
Pressures were applied on sham points consecutively

Locations

Country Name City State
Egypt Faculty of physical therapy Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Anxiety level To measure anxiety, the Spiberger inventory questionnaire will be used about one hour
Primary labor pain labor pain will be assessed using visual analogue scale.
. It employs a 10-cm ruler scale with no pain sign at one end and the most intense pain sign at the other to allow users to assess their own pain
about one hour
Secondary pulse rate response will measured using pulse oximetry about one hour
Secondary blood pressure response will measured using sphygmomanometer about one hour
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