CompletedNot Applicable

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

Turkey (Türkiye)30 participantsStarted 2025-03-01

Plain-language summary

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.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Systolic Blood Pressure

Timeframe: baseline, 15 minutes, 60 minutes, 4 hours after intervention

Heart Rate (Pulse Rate)

Timeframe: baseline, 15 minutes, 60 minutes, 4 hours after intervention

Oxygen Saturation (SpO₂)

Timeframe: baseline, 15 minutes, 60 minutes, 4 hours after intervention

Body Temperature

Timeframe: baseline, 15 minutes, 60 minutes, 4 hours after intervention

Respiratory Rate

Timeframe: baseline, 15 minutes, 60 minutes, 4 hours after intervention

Richmond Agitation-Sedation Scale (RASS)

Timeframe: baseline, 1 hour, 4 hours after intervention

Behavioral Pain Scale (BPS)

Timeframe: baseline, 1 hour, 4 hours after intervention

Trial details

NCT IDNCT07632781

SponsorHasan Kalyoncu University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-03-01

View on ClinicalTrials.gov More Intensive Care Unit Patients trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Systolic Blood Pressure

Timeframe: baseline, 15 minutes, 60 minutes, 4 hours after intervention

Heart Rate (Pulse Rate)

Timeframe: baseline, 15 minutes, 60 minutes, 4 hours after intervention

Oxygen Saturation (SpO₂)

Timeframe: baseline, 15 minutes, 60 minutes, 4 hours after intervention

Body Temperature

Timeframe: baseline, 15 minutes, 60 minutes, 4 hours after intervention

Respiratory Rate

Timeframe: baseline, 15 minutes, 60 minutes, 4 hours after intervention

Richmond Agitation-Sedation Scale (RASS)

Timeframe: baseline, 1 hour, 4 hours after intervention

Behavioral Pain Scale (BPS)

Timeframe: baseline, 1 hour, 4 hours after intervention