THE EFFECT OF SU-JOK THERAPY APPLIED TO INTENSİVE CARE PATIENTS UNDER MECHANICVENTILATION SUPPORT
THE EFFECT OF SU-JOK THERAPY APPLIED TO INTENSIVE CARE PATIENTS UNDER MECHANICAL VENTILATION SUPPORT ON PAIN AND PHYSIOLOGICAL PARAMETERS.
調査の概要
詳細な説明
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.
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
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Kahramanmaraş
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Kahramanmaraş、Kahramanmaraş、トルコ（Türkiye）、46050
- Kahramanmaraş
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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.
研究計画
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：処理
- 割り当て：ランダム化
- 介入モデル：並列代入
- マスキング：独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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介入なし：対照群
対照群には介入は適用されません。
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実験的：Intervetion group
In the intervention group, su-jok seed therapy will be applied to the su-jok reflection zones on the hands.
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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.
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プラセボコンパレーター：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.
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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.
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この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Systolic Blood Pressure
時間枠：baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Hemodynamic response measured by systolic blood pressure
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baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Heart Rate (Pulse Rate)
時間枠：baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Heart rate measured in beats per minute
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baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Oxygen Saturation (SpO₂)
時間枠：baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Peripheral oxygen saturation
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baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Body Temperature
時間枠：baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Core body temperature
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baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Respiratory Rate
時間枠：baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Number of breaths per minute
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baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Richmond Agitation-Sedation Scale (RASS)
時間枠：baseline, 1 hour, 4 hours after intervention
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Negative scores indicate sedation, positive scores indicate agitation
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baseline, 1 hour, 4 hours after intervention
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Behavioral Pain Scale (BPS)
時間枠：baseline, 1 hour, 4 hours after intervention
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Higher scores indicate more severe pain
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baseline, 1 hour, 4 hours after intervention
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Hemodynamic Stability Index (Systolic/Diastolic Blood Pressure Change)
時間枠：baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Change in systolic and diastolic blood pressure from baseline to post-intervention measurements.
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baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Oxygenation Trend (SpO₂ Change Over Time)
時間枠：baseline, 15 minutes, 60 minutes, 4 hours after intervention
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hanges in peripheral oxygen saturation over the intervention period.
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baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Heart Rate Variability (Clinical Pulse Trend)
時間枠：baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Changes in heart rate measured in beats per minute during and after intervention.
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baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Sedation-Agitation Level Stability (RASS Trend)
時間枠：baseline, 1 hour, 4 hours after intervention
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Changes in Richmond Agitation-Sedation Scale (RASS) scores over time indicating sedation or agitation level.
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baseline, 1 hour, 4 hours after intervention
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Pain Intensity Change (Behavioral Pain Scale Trend)
時間枠：baseline, 1 hour, 4 hours after intervention
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Changes in Behavioral Pain Scale (BPS) scores indicating pain severity over time.
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baseline, 1 hour, 4 hours after intervention
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Respiratory Stability (Respiratory Rate Change)
時間枠：baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Changes in respiratory rate indicating respiratory stability during intervention.
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baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Temperature Stability
時間枠：baseline, 15 minutes, 60 minutes, 4 hours after intervention
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hanges in body temperature over time following intervention.
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baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Non-pharmacological Intervention Effectiveness (Overall Clinical Stability Score)
時間枠：baseline, 4 hours after intervention
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Composite assessment of physiological stability based on vital signs and sedation/pain scores.
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baseline, 4 hours after intervention
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協力者と研究者
捜査官
- スタディチェア：NERMİN OLGUN, Prof. Dr.、Hasan Kalyoncu University
- 主任研究者：MELTEM KALAYCI、Hasan Kalyoncu University
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- HKU-LEE-MK-01
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