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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05799547
Other study ID # 55555
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 20, 2023
Est. completion date August 20, 2023

Study information

Verified date April 2023
Source Osmaniye Korkut Ata University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A healthy postpartum period is important for the health of the mother and baby. One of the main problems that occur after cesarean section, which is a major surgical procedure, is pain. However, since the mother is in the postpartum period, she may have problems in her own care, healing process and baby care due to pain. Non-pharmacological treatment is methods such as massage, acupressure, hot and cold application that can be applied at birth to support scientific medicine. The cold application examined in our research, is among these applications. participants will be determined by the block randomization method. Cold application will be applied to the cesarean section site of the patient for 10 minutes in the experimental group, followed by a break of 20 minutes, followed by a 10-minute application, and immediately after the application, the patient will stand up. Only the routine practice of the clinic will be applied to the control group. Data; will be collected using the introductory information form, visual analog scale (VAS) and cold application satisfaction evaluation form. When the studies were examined, no other study was found in the same application as our study. Therefore, in this study, it was aimed to evaluate the effect of cold application on the patient's pain during the first leg, the need for painkillers and satisfaction, due to the higher first take-off pain after cesarean section.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date August 20, 2023
Est. primary completion date July 10, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - Postpartum women who had cesarean section surgery - Having had a previous cesarean section, Exclusion Criteria: - Those who have problems in postpartum vital signs and bleeding control - Those who have systemic diseases that may affect cold application - Those who are distressed and not suitable for practice by the service midwives and doctors, - Those who do not want to participate in the research

Study Design


Related Conditions & MeSH terms


Intervention

Other:
cold group
Application will be made in the form of 10 minutes of application to the cesarean section incision, 20 minutes of break and 10 minutes of application.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Osmaniye Korkut Ata University

Outcome

Type Measure Description Time frame Safety issue
Primary visual analog scale (VAS) The visual analog scale is used to assess pain. The person marks the pain he feels on a ten-centimeter chart that expresses the absence of pain on one side and the pain he feels at the peak on the other side. 1 week
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