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Clinical Trials in Turkey / NCT07432074
Enrolling by invitation Not applicable

The Effects of Acupressure and Massage Following Cesarean Section

NCT07432074 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-02-20
Last updated
2026-02-25

Condition(s) studied

Pain ManagementSleep QualityMassage EffectAcupressureFatigue

Investigational drug(s) / intervention(s)

Acupressure to points HT7, LI4, SP6 and ST36Massage

Acupressure to points HT7, LI4, SP6 and ST36: This point specialized for pain management, fatigue and sleep

Massage: back massage

Study summary

Cesarean section births have rapidly increased both in our country and worldwide in recent years. According to OECD data, one in four births worldwide and one in two births in our country is a cesarean section. The cesarean section has become one of the most frequently performed surgical interventions. The incision from a cesarean section causes pain, mobilization issues, and delays in mother-infant interaction. The choice of pharmacological methods used after a cesarean section is often limited by concerns about the baby and breastfeeding, leading to inadequate pain management and causing women to experience moderate to high levels of pain. Pain negatively affects individuals' comfort, leading to sleep disturbances, fatigue, and a decreased quality of life. It makes daily activities and responsibilities as individuals more challenging to manage. There is a need for nurses, in their primary caregiver role, to adopt a multidisciplinary approach to pain management and to develop their skills in using non-pharmacological methods. These methods should be clinically applied and proven effective. Acupressure and massage are long-standing, cost-effective, easy-to-apply, and effective methods used to reduce pain. This study aims to reduce pain and fatigue and improve sleep quality in women who have undergone a cesarean section by applying acupressure and massage in the postoperative period, thereby preventing the chronicization of these problems.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
45 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Women aged 18-45 years * Undergoing cesarean delivery under spinal anesthesia, * Having a term, single, and healthy newborn, * Gestational age of 37-40 weeks, * No communication difficulties, * No systemic or chronic diseases, * Willing to participate in the study. Exclusion Criteria: * Undergoing cesarean delivery under general or epidural anesthesia, * Development of any maternal or neonatal complications during the postpartum period (hypertension, hemorrhage, infants requiring intensive care, etc.), * Having chronic fatigue or pain problems, * Using caffeine (tea, coffee, chocolate, etc.).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Marmara University Istanbul Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07432074 on ClinicalTrials.gov ↗ ← All trials in Turkey