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Enrolling by invitation NCT07432074

The Effects of Acupressure and Massage Following Cesarean Section

No phase Interventional Pain Management Sleep Quality Massage Effect Acupressure

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Acupressure to points HT7, LI4, SP6 and ST36, Massage.
Who it may be relevant to
Registry conditions: Pain Management, Sleep Quality, Massage Effect, Acupressure. Basic parameters: 18 years — 45 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effects of Acupressure and Back Massage on Pain, Fatigue, and Sleep Quality in Cesarean Sections: A Randomized Controlled Study

Overview

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.

Interventions

  • Other Acupressure to points HT7, LI4, SP6 and ST36
    This point specialized for pain management, fatigue and sleep
  • Other Massage
    back massage

Primary outcome measures

  • Visual Analog Scale for Pain [Time frame: Periprocedural (immediately after the intervention or standard care)]
Secondary outcome measures (2)
  • Postpartum Sleep Quality Scale [Time frame: 15 minutes after completion of the intervention]
  • Postnatal Accumulated Fatigue Scale [Time frame: 15 minutes after completion of the intervention]

Eligibility criteria

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.).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Factorial
Masking
Open label
Primary purpose
Supportive care

Study locations

Turkey (Türkiye) · 1 center
  • Marmara University — Istanbul

Identifiers

NCT: NCT07432074 · marmaradeneysel

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗