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EFFECT OF KINESIO TAPING ON POST-C-SECTION PAIN AND COMFORT

EFFECT OF KINESIO TAPING ON POST-C-SECTION PAIN AND COMFORT

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06622707
Enrollment
60
Registered
2024-10-02
Start date
2024-11-05
Completion date
2025-03-02
Last updated
2024-10-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

C-Section

Keywords

Kinesio Taping, Pain, Postpartum Comfort

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.

Interventions

OTHERkinesio taping

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

Sponsors

Şırnak Üniversitesi
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
19 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* 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.

Exclusion criteria

* 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,

Design outcomes

Primary

MeasureTime frameDescription
vasVAS will be applied at the 10th hour, 24th hour, 48th hour and 72nd hour after cesarean section.It is used to measure subjectively perceived pain
Postpartum comfort questionnaireIt will be filled in at the 10th and 72th hours after birth.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.

Contacts

Primary ContactKübra akcan lecturer
kbr_akcn@outlook.com5319445935

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026