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- Essai clinique NCT07632781
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.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
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.
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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Kahramanmaraş
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Kahramanmaraş, Kahramanmaraş, Turquie (Türkiye), 46050
- Kahramanmaraş
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
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.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Aucune intervention: Groupe de contrôle
Aucune intervention ne sera appliquée au groupe témoin.
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Expérimental: 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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Comparateur placebo: 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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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Systolic Blood Pressure
Délai: baseline, 15 minutes, 60 minutes, 4 hours after intervention
|
Hemodynamic response measured by systolic blood pressure
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baseline, 15 minutes, 60 minutes, 4 hours after intervention
|
|
Heart Rate (Pulse Rate)
Délai: 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)
Délai: baseline, 15 minutes, 60 minutes, 4 hours after intervention
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Peripheral oxygen saturation
|
baseline, 15 minutes, 60 minutes, 4 hours after intervention
|
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Body Temperature
Délai: baseline, 15 minutes, 60 minutes, 4 hours after intervention
|
Core body temperature
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baseline, 15 minutes, 60 minutes, 4 hours after intervention
|
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Respiratory Rate
Délai: baseline, 15 minutes, 60 minutes, 4 hours after intervention
|
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)
Délai: 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)
Délai: 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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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Hemodynamic Stability Index (Systolic/Diastolic Blood Pressure Change)
Délai: 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
|
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Oxygenation Trend (SpO₂ Change Over Time)
Délai: 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
|
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Heart Rate Variability (Clinical Pulse Trend)
Délai: 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
|
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Sedation-Agitation Level Stability (RASS Trend)
Délai: 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)
Délai: 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)
Délai: 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
Délai: 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)
Délai: baseline, 4 hours after intervention
|
Composite assessment of physiological stability based on vital signs and sedation/pain scores.
|
baseline, 4 hours after intervention
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chaise d'étude: NERMİN OLGUN, Prof. Dr., Hasan Kalyoncu University
- Chercheur principal: MELTEM KALAYCI, Hasan Kalyoncu University
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- HKU-LEE-MK-01
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
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