Healing hands: touch therapy may soothe ICU agitation and pain
NCT ID NCT07061340
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether therapeutic touch—a gentle, non-invasive therapy—can help reduce agitation, pain, and stress hormone levels in intensive care patients. About 60 adults who are awake and stable in the ICU will either receive this touch therapy or standard care. The goal is to see if this simple, drug-free approach can improve comfort and recovery.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2025
An estimate. Start dates often move.
- Expected to finish
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Jul 2026
An estimate. End dates often move.
- 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 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Adults aged 18 years and above. * Patients who can communicate verbally. * Patients who have been monitored in the intensive care unit for at least 4 days. * Patients who are able to give informed consent. * Patients who are hemodynamically stable. * Richmond Agitation-Sedation Scale 1 and above. * Visual Analog Scale 1 and above. Exclusion Criteria: 1. Patients under deep sedation. 2. Patients on mechanical ventilation. 3. Patients with psychiatric problems. 4. Patients with skin diseases or open wounds, infections, burns that would prevent therapeutic touch. 5. Patients using sedative/analgesic drugs (excessive sedation or delirium). 6. Patients using corticosteroids or drugs that affect adrenal hormone levels (because these drugs can affect cortisol measurements). 7. Patients who have sudden life-threatening clinical changes during intensive care (e.g. sudden cardiac arrest, shock).
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Fırat university
Elâzığ, Center, 25240, Turkey (Türkiye)
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