Healing hands: therapeutic touch may ease pain and delirium in ICU patients
NCT ID NCT07404904
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether therapeutic touch — a gentle, non-invasive technique — can reduce pain, delirium, and improve sleep in 80 intensive care patients. Researchers measured pain, sedation, sleep quality, and vital signs like blood pressure and heart rate. The goal was to see if this simple, drug-free approach could make ICU stays more comfortable.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- therapeutic touch (a gentle, non-invasive hands-on technique)
- What this could lead to
- If it works, this could offer a drug-free way to ease pain and improve sleep for intensive care patients.
- What could go wrong
- This is a small, completed study with no blinding, so results may be influenced by placebo effects. The approach is not a cure and may not work for everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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80 people
The number who actually took part.
- Started
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Oct 2024
- Finished
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Feb 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients who volunteer to participate in the study, * Patients aged 18 and over who receive post-surgical treatment at the Surgical Intensive Care Unit of Aksaray Education and Research Hospital, * Patients who do not have communication problems (hearing, speaking, understanding, etc.), * Patients who have received treatment in the surgical intensive care unit for at least 72 hours, * Patients with RASS: between -3 and +4 and Glasgow coma scale: 10 and above, * Patients who use only non-steroidal drugs as analgesics, * Patients whose medical diagnosis is not dementia, * Patients who do not have a mental state disorder/psychological disease and do not use sleeping pills. Exclusion Criteria: * Patients who developed complications in the ICU after surgery, * Patients who received treatment in the surgical intensive care unit for less than 72 hours.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Aksaray Universitesi
Aksaray, 68100, Turkey (Türkiye)
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