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Not yet recruiting NCT06760013

The Effect of Su-jok Therapy Applied in the First Stage of Labor on Pain Level in Primiparas

No phase Interventional Labor Pain

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: Su Jok Therapy.
Who it may be relevant to
Registry conditions: Labor Pain. Basic parameters: 18 years — 60 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 →

Overview

The aim of this study is to examine the effect of sujok therapy applied in the first stage of labor on the pain level in primiparas.

Detailed description

Birth pain, known as acute pain, is felt in the human body as one of the oldest, complex, severe and most difficult to control types of pain. However, this pain differs from other types of pain due to the fact that it reunites the mother with her baby and covers a limited period of time. Pain is a subjective phenomenon that every individual experiences throughout their lives and to which people react differently.

Su Jok therapy, an alternative and complementary therapy technique, is seen as a method that balances the energy flow based on the philosophy of non-pharmacological and non-invasive acupuncture that can be used to control labor pain.

Su-jok application is the development of a massage therapy that will create a feeling of comfort in the body by using certain points. There are tiny swellings on the reflection points on the hands and feet (such as the area between the 3rd and 4th fingers reflecting the uterus area). These are also called micro acupuncture points. When pressure is applied to these swellings on the hands and feet for 1-2 minutes, pain and a feeling of pulling occur. Thus, the area to be massaged is determined. During the detection phase, a blunt-tipped diagnostic probe or a round-tipped stick can be used. At this stage, the same amount of pressure should be applied to the area to be applied. When a point is determined, the correct point for massage application should be massaged and energy flow should be provided. Since it does not have any side effects, it is a therapy that can be used in pregnant women and is a massage application that does not require any invasive intervention.

Interventions

  • Behavioral Su Jok Therapy
    The researcher, who has a Su-Jok practitioner certificate, applied pressure for 1-2 minutes on the active point on the meridian (the area between the 3rd and 4th fingers pointing to the uterus) that provides energy flow in the palm in 20-minute periods, with the help of a diagnostic probe (diagnostic stick). The point will be determined. Once this point is detected, a massage will be performed on the point. The massage will be applied with a 10-minute rest period between each two periods.

Primary outcome measures

  • Visual Analog Scale (VAS) [Time frame: eight months]
Secondary outcome measures (2)
  • MONITORING FORM FOR BIRTH (FOR SU JOK GROUP) [Time frame: eight months]
  • MONITORING FORM FOR BIRTH (CONTROL GROUP) [Time frame: eight months]

Eligibility criteria

Inclusion criteria

  • Being primiparous
  • The pregnant woman must be over 18 years of age
  • To participate in the research voluntarily
  • The beginning of labor (water breaking, presence of non-stress testa contractions, engagement)

Exclusion criteria

  • Pregnancies outside 37-41 weeks
  • Multiparas
  • Those who are not pregnant
  • Having visual, mental and auditory disabilities
  • Being pregnant as an adolescent
  • Not accepting participation in the research

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
Parallel assignment
Masking
Open label
Primary purpose
Supportive care

Study locations

Turkey (Türkiye) · 1 center
  • Hitit University — Çorum

Identifiers

NCT: NCT06760013 · HU-SBF-ARA-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗