EFFECT OF KINESIO TAPING ON POST-C-SECTION PAIN AND COMFORT
1 other identifier
interventional
60
0 countries
N/A
Brief Summary
Kinesio taping gently stretches the skin and creates a gap between the dermis and fascia, increasing lymphatic and vascular flow and reducing pain without restricting movement. It is used to provide rehabilitation after surgical operations. This study will be conducted to determine the effect of kinesio taping on the mother\'s pain and comfort after cesarean section. It is planned to include 60 women who gave birth by cesarean section in the obstetrics and gynecology department at Şırnak State Hospital. Research data will be collected with the visual analog scale and postpartum comfort scale. If the data shows normal distribution, Unrelated Samples t Test, Related Samples t Test and Repeated Measures ANOVA (Repeated Measures) tests will be used.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2024
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 29, 2024
CompletedFirst Posted
Study publicly available on registry
October 2, 2024
CompletedStudy Start
First participant enrolled
November 5, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 20, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 2, 2025
CompletedOctober 2, 2024
September 1, 2024
3 months
September 29, 2024
September 29, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
vas
It is used to measure subjectively perceived pain
VAS will be applied at the 10th hour, 24th hour, 48th hour and 72nd hour after cesarean section.
Postpartum comfort questionnaire
It is a scale that can be used appropriately and safely in measuring the postpartum comfort of mothers who have given birth normally or by cesarean section, in meeting the postpartum comfort needs, and in evaluating the outcome as a concrete indicator of the outcome.
It will be filled in at the 10th and 72th hours after birth.
Study Arms (2)
kinesio taping group
EXPERIMENTALKinesio taping will be applied to this group.
control group
EXPERIMENTALParticipants in this group will not receive any intervention other than routine clinical care.
Interventions
Despite the increasing indications and new application techniques developed all over the world, it is believed that there is a need for evidence regarding the mechanisms of action and effectiveness of kinesio taping. As a result of the literature review, no study was found in which kinesio taping was applied for 72 hours as a non-pharmacological complementary method to reduce postoperative pain after cesarean section and increase postpartum comfort. In this study, it is planned to apply kinesiotaping for 72 hours after cesarean section.
As routine clinical care; Analgesic treatment protocol applied after cesarean section, postnatal care and discharge services are provided
Eligibility Criteria
You may qualify if:
- patients having C-section delivery in the 37th and 40th gestational weeks,
- patients giving birth to just a baby,
- patients with no chronic disease (such as allergy, diabetes, or hypertension),
- patients having no problems with communication,
- patients with no dermatological disease.
You may not qualify if:
- patients whose babies are in the neonatal intensive care unit,
- patients with deep vein thrombosis, open wounds, or skin irritation,
- patients who did not want to participate in the study,
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- lecturer
Study Record Dates
First Submitted
September 29, 2024
First Posted
October 2, 2024
Study Start
November 5, 2024
Primary Completion
January 20, 2025
Study Completion
March 2, 2025
Last Updated
October 2, 2024
Record last verified: 2024-09
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
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