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

Sponsor
Osmaniye Korkut Ata University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05799547
Collaborator
(none)
30
2
2

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: cold group
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Other
Official Title:
The Effect of Cold Application on the Pain, Comfort and Satisfaction of the Patient on First Standing After Cesarean Section
Anticipated Study Start Date :
Jun 20, 2023
Anticipated Primary Completion Date :
Jul 10, 2023
Anticipated Study Completion Date :
Aug 20, 2023

Arms and Interventions

Arm Intervention/Treatment
No Intervention: control group

Experimental: experimental group

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.

Outcome Measures

Primary Outcome Measures

  1. visual analog scale (VAS) [1 week]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Osmaniye Korkut Ata University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Emine Yıldırım, Assistant Professor, Osmaniye Korkut Ata University
ClinicalTrials.gov Identifier:
NCT05799547
Other Study ID Numbers:
  • 55555
First Posted:
Apr 5, 2023
Last Update Posted:
Apr 5, 2023
Last Verified:
Apr 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Apr 5, 2023