이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

THE EFFECT OF SU-JOK THERAPY APPLIED TO INTENSİVE CARE PATIENTS UNDER MECHANICVENTILATION SUPPORT

2026년 6월 2일 업데이트: MELTEM KALAYCI, Hasan Kalyoncu University

THE EFFECT OF SU-JOK THERAPY APPLIED TO INTENSIVE CARE PATIENTS UNDER MECHANICAL VENTILATION SUPPORT ON PAIN AND PHYSIOLOGICAL PARAMETERS.

The aim of this study is to examine the effect of Su Jok Therapy, applied to patients receiving mechanical ventilation support in the intensive care unit, on pain and physiological parameters.

연구 개요

상세 설명

Mechanical ventilation (MV), one of the most common treatment methods in Intensive Care Units (ICUs), is a critical treatment approach to ensure adequate respiratory function in patients.

Although mechanical ventilation is a life-saving treatment method in ICUs, it can cause many physiological and psychological problems for patients. Furthermore, excessive exposure to physical, psychosocial, and environmental stressors can affect the patient's autonomic response and vital parameters (tachycardia, hypertension, tachypnea), leading to hemodynamic instability

The World Health Organization (WHO) defines Integrated, Complementary, and Alternative Medicine Practices as the provision of healthcare services that are not part of a country's own tradition or conventional medicine and are not fully integrated into the dominant healthcare system In intensive care patients, non-pharmacological methods such as aromatherapy, music therapy, massage, reflexology, acupressure, and Reiki are used as complementary and alternative treatments. Su Jok, one of these non-pharmacological methods, is an alternative treatment method based on traditional Korean medicine. Su Jok is a treatment method that uses the feet and hands, derived from the Korean words Su (hand) and Jok (foot). In the literature, it is argued that nurses can apply Su Jok therapy as an integrative method in symptom management due to its simplicity of application, lack of side effects, and non-invasiveness, which is similar to the philosophy of integrative nursing. Looking at the literature, very few studies on Su Jok therapy have been found. No studies have been found in the literature regarding the effect of Su Jok therapy on intensive care patients and patients on mechanical ventilation support.

연구 유형

중재적

등록 (실제)

30

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Kahramanmaraş
      • Kahramanmaraş, Kahramanmaraş, 터키 (Türkiye), 46050
        • Kahramanmaraş

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria:

  • Patients who are in intensive care,

    • Patients receiving IMV support,
    • Patients who were admitted to the ICU from the start date of the study and are planned to be monitored for at least 24 hours,
    • Patients without any problems in the area where Su-Jok will be applied,
    • Patients with GCS > 3, RASS between +1 and +4, BPS > 3

Exclusion Criteria:

  • • Patients in the ward,

    • Patients with any problems such as fungal infections or wounds in the area where Su Jok will be applied,
    • Patients with a GCS of 3,
    • Patients not receiving IMV support will not be included in the study.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 하나의

무기와 개입

참가자 그룹 / 팔
개입 / 치료
간섭 없음: 대조군
통제 그룹에는 개입이 적용되지 않습니다.
실험적: Intervetion group
In the intervention group, su-jok seed therapy will be applied to the su-jok reflection zones on the hands.
In the intervention group, the reflex zones on the hands were identified with a probe. Buckwheat seeds were fixed to these areas with adhesive tape and massaged. The seeds remained in place for 4 hours. After 2 hours, these areas were stimulated with a 1-2 minute massage. Measurements were recorded on a data collection form. The application was carried out for 3 days.
위약 비교기: Placebo group
In the placebo group, su-jok seed therapy will be applied to areas on the hands that are different from the reflection zones.
In the placebo group, reflex zones on the hand were identified using a probe. Buckwheat seeds were fixed to a different area near these zones with a seed patch and massaged. The seeds remained in place for 4 hours. After 2 hours, these areas were stimulated with a 1-2 minute massage. Measurements were recorded on a data collection form. The application was carried out for 3 days.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Systolic Blood Pressure
기간: baseline, 15 minutes, 60 minutes, 4 hours after intervention
Hemodynamic response measured by systolic blood pressure
baseline, 15 minutes, 60 minutes, 4 hours after intervention
Heart Rate (Pulse Rate)
기간: baseline, 15 minutes, 60 minutes, 4 hours after intervention
Heart rate measured in beats per minute
baseline, 15 minutes, 60 minutes, 4 hours after intervention
Oxygen Saturation (SpO₂)
기간: baseline, 15 minutes, 60 minutes, 4 hours after intervention
Peripheral oxygen saturation
baseline, 15 minutes, 60 minutes, 4 hours after intervention
Body Temperature
기간: baseline, 15 minutes, 60 minutes, 4 hours after intervention
Core body temperature
baseline, 15 minutes, 60 minutes, 4 hours after intervention
Respiratory Rate
기간: baseline, 15 minutes, 60 minutes, 4 hours after intervention
Number of breaths per minute
baseline, 15 minutes, 60 minutes, 4 hours after intervention
Richmond Agitation-Sedation Scale (RASS)
기간: baseline, 1 hour, 4 hours after intervention
Negative scores indicate sedation, positive scores indicate agitation
baseline, 1 hour, 4 hours after intervention
Behavioral Pain Scale (BPS)
기간: baseline, 1 hour, 4 hours after intervention
Higher scores indicate more severe pain
baseline, 1 hour, 4 hours after intervention

2차 결과 측정

결과 측정
측정값 설명
기간
Hemodynamic Stability Index (Systolic/Diastolic Blood Pressure Change)
기간: baseline, 15 minutes, 60 minutes, 4 hours after intervention
Change in systolic and diastolic blood pressure from baseline to post-intervention measurements.
baseline, 15 minutes, 60 minutes, 4 hours after intervention
Oxygenation Trend (SpO₂ Change Over Time)
기간: baseline, 15 minutes, 60 minutes, 4 hours after intervention
hanges in peripheral oxygen saturation over the intervention period.
baseline, 15 minutes, 60 minutes, 4 hours after intervention
Heart Rate Variability (Clinical Pulse Trend)
기간: baseline, 15 minutes, 60 minutes, 4 hours after intervention
Changes in heart rate measured in beats per minute during and after intervention.
baseline, 15 minutes, 60 minutes, 4 hours after intervention
Sedation-Agitation Level Stability (RASS Trend)
기간: baseline, 1 hour, 4 hours after intervention
Changes in Richmond Agitation-Sedation Scale (RASS) scores over time indicating sedation or agitation level.
baseline, 1 hour, 4 hours after intervention
Pain Intensity Change (Behavioral Pain Scale Trend)
기간: baseline, 1 hour, 4 hours after intervention
Changes in Behavioral Pain Scale (BPS) scores indicating pain severity over time.
baseline, 1 hour, 4 hours after intervention
Respiratory Stability (Respiratory Rate Change)
기간: baseline, 15 minutes, 60 minutes, 4 hours after intervention
Changes in respiratory rate indicating respiratory stability during intervention.
baseline, 15 minutes, 60 minutes, 4 hours after intervention
Temperature Stability
기간: baseline, 15 minutes, 60 minutes, 4 hours after intervention
hanges in body temperature over time following intervention.
baseline, 15 minutes, 60 minutes, 4 hours after intervention
Non-pharmacological Intervention Effectiveness (Overall Clinical Stability Score)
기간: baseline, 4 hours after intervention
Composite assessment of physiological stability based on vital signs and sedation/pain scores.
baseline, 4 hours after intervention

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 연구 의자: NERMİN OLGUN, Prof. Dr., Hasan Kalyoncu University
  • 수석 연구원: MELTEM KALAYCI, Hasan Kalyoncu University

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2025년 3월 1일

기본 완료 (실제)

2025년 3월 1일

연구 완료 (실제)

2025년 11월 1일

연구 등록 날짜

최초 제출

2025년 12월 30일

QC 기준을 충족하는 최초 제출

2026년 6월 2일

처음 게시됨 (실제)

2026년 6월 8일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 8일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 6월 2일

마지막으로 확인됨

2026년 6월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

구독하다