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Starting soon Not applicable

The Effect of Su Jok Application on Pain, Anxiety and Comfort Levels After Cesarean Section

NCT07091760 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-09-01
Last updated
2025-07-29

Condition(s) studied

Caesarean Section

Investigational drug(s) / intervention(s)

Su Jok ApplicationPlacebo Application

Su Jok Application: The patient's hands will be preferred for the application due to the comfort and convenience of the woman after cesarean section. Su Jok therapy, massage and seed will be applied to the reflection points on the hand based on the area to be treated.

Placebo Application: Placebo Intervention: The placebo group will be massaged and seed will be applied to an area where there is no reflection of the Su Jok organ.

Study summary

Objective: To determine the effect of Su Jok application on pain, anxiety and comfort level after cesarean section. The research will be conducted as a randomized controlled experimental study with pretest-posttest control group

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
35 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Being between 18-35 years of age * Having at least primary school education * Not having any health problems (such as hypertension, tuberculosis, cancer) * Not having hearing and vision problem * Having a cesarean section with regional anesthesia * Being within the first 48 hours after the operation * Not having any wounds or infectious diseases in their hands * Not having a diagnosis of psychiatric disease * Speaking Turkish, women who voluntarily agreed to participate in the study. Exclusion Criteria: * Postpartum hemorrhage * Incomplete completion of the application stages * Complications during the application process * Voluntary withdrawal of the woman from the study.

Primary outcome measure(s)

  • Personal Information Form — 10 months
    There are 21 questions in this form, prepared by the researchers in line with the literature
  • Visual Analog Scale (VAS) — 10 months
    The Visual Analog Scale is an assessment tool in which patients mark on a 10 cm ruler. The 10 cm scale, which is a numerical pain assessment scale, starts with "No pain (0)" and ends with "Intolerable pain (10)". The patient is asked to mark the place on the line that expresses pain. The distance marked by the patient is measured by taking zero as the starting distance. In this way, the patient's pain level is determined. In this study, a horizontal VAS will be used to assess pain intensity. The reason for choosing this scale in the study is that it is easy to understand and easy to use by the participants.
  • Verbal Category Scale — 10 months
    The scale is based on the selection of the most appropriate word to describe the patient's pain condition. The pain of the patients is evaluated with the scoring method 'No Pain 0 points, Very Mild Pain 2 points, Mild Pain 4 points, Severe Pain 6 points, Very Severe Pain 8 points, Unbearable Pain 10 points'. The patient will be asked to select the appropriate pain level. The scale is easy to apply and easy to classify.
  • Spielberg State Anxiety Scale — 10 months
    This scale was developed by Spielberger et al. Developed by. The adaptation of the scale to Turkish and its validity and reliability studies were carried out by Öner and Le Compte in 1983.The scale is a 4-point Likert scale consisting of the options "not at all", "somewhat", "a lot", "completely". There are 10 direct and 10 reversed statements in the scale. Positive (increasing the total anxiety score) for items 3, 4, 6, 7, 9, 12, 13, 14, 17, 18 in the scale; 1, 2, 5, 8, 10, 11, 15, 16, 19 Negative scores (reducing the total anxiety score) are obtained for the 20th items. The highest score is 80 and the lowest score is 20. A high total score indicates that the person's anxiety level is also high.Cronbach's alpha coefficient was found to be 0.79 for state anxiety. In this study, Cronbach's Alpha value was found to be 0.83.
  • Postpartum Comfort Scale — 10 months
    The scale developed by Karakaplan and Yıldız (2010) to determine women's comfort after cesarean delivery and vaginal delivery is Likert-type and consists of 34 items. Each item is scored between "strongly disagree" (1 point) and "strongly agree" (5 points). The lowest score that can be obtained from the scale is 34 and the highest score is 170. The scale consists of three sub-dimensions (physical, psychosocial and sociocultural). An increase in the score obtained from the scale indicates an increase in comfort. Cronbach Alpha internal consistency coefficient was calculated as 0.78.

Trial sites (1)

FacilityCityRegionStatus
Ataturk University Erzurum Turkey (Türkiye)
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 NCT07091760 on ClinicalTrials.gov ↗ ← All trials in Turkey