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

NCT ID: NCT06760013

Last Updated: 2025-01-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-01-15

Study Completion Date

2025-08-30

Brief Summary

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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

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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.

Conditions

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Labor Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

It is planned to have a Randomized Control experimental design in two groups.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Su jok therapy group

Sujok massage therapy will be applied to the affected area on the hands of pregnant women who will give birth for the first time.

Group Type ACTIVE_COMPARATOR

Su Jok Therapy

Intervention Type BEHAVIORAL

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.

Control Group

A comparison will be made on this group with pregnant women who receive sujok therapy without any therapy.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Hitit University

OTHER

Sponsor Role lead

Responsible Party

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AYSUDA REFİYE AKVERAN

Graduate Student

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Hitit University

Çorum, Merkez, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Central Contacts

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AYSUDA R AKVERAN

Role: CONTACT

+90 534-610-2318

Facility Contacts

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AYSUDA R AKVERAN

Role: primary

+90 534-610-2318

Other Identifiers

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HU-SBF-ARA-01

Identifier Type: -

Identifier Source: org_study_id

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