Effect of Acupressure Point Liv3 on postpartum pain reductio
- Conditions
- Postpartum pain.Routine postpartum follow-up
- Registration Number
- IRCT20100503003860N35
- Lead Sponsor
- Dept. of Research, School of Nursing and Midwifery, Shaheed Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 150
1- be Iranian. 2- Have at least the ability to read and write. 3- All 20-35 years-old mothers who have complained of postpartum pain and at least two hours have passed since their delivery and report a score of 4 or more on the basis of a pain ruler. 4- Child birth by vaginal delivery. 5- To have Gestational age 38 weeks or more. 6- Not used for epidural anesthesia. 7- No drug or alcohol addiction. 8- Do not smoke. 9- There are no Skin disease, mole, burnt, wound, fracture, tendon and muscle problems in the legs. 10- There are no known medical or mental illnesses based on the case (liver diseases, diabetes, coagulation disorders, hemophilia, immune deficiency). 11- There are no conflicts and family conflicts and severe financial problems during the last 6 months. 12- Pregnancy is unwanted. 13- Have a baby live and without abnormalities.
1- Do not wish to continue with the researcher. 2- Mothers who need surgery and receive postpartum anesthetic. 3- Mothers who have been discharged with personal satisfaction before 12 hours.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post-partum pain. Timepoint: Before the intervention, 30 minutes and 2 hours after taking the pill, every 6 hours after the intervention. Method of measurement: Pain ruler (numerical scale).
- Secondary Outcome Measures
Name Time Method Description: Possible side effects of intervention. Timepoint: Timepoint: At the end of intervention period. Method of measurement: Method of measurement: At the end of the intervention period.