The Effect of Cold Application on Patient's Pain, Comfort and Satisfaction After Cesarean Section

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-06-20

Study Completion Date

2023-08-20

Brief Summary

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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.

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Detailed Description

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Conditions

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Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Study Groups

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control group

Group Type NO_INTERVENTION

No interventions assigned to this group

experimental group

Group Type EXPERIMENTAL

cold group

Intervention Type OTHER

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.

Interventions

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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.

Intervention Type OTHER

Eligibility Criteria

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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

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes