Tiny hands, big relief? su jok therapy tested for newborn pain
NCT ID NCT07164820
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tests whether Su Jok therapy—a technique using hand massage and seeds on specific points—can lower pain in newborns during a heel lance blood test. Sixty-six full-term babies will be randomly assigned to receive the therapy or standard care. Pain will be measured using a validated scale by experienced nurses and doctors.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Su Jok therapy (hand massage and seed application)
- What this could lead to
- If it works, this could offer a simple, drug-free way to ease pain in newborns during routine blood tests.
- What could go wrong
- This is a small, early-stage trial with only 66 babies. The therapy may not reduce pain significantly, and results may not apply to all newborns.
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
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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 66 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2025
An estimate. Start dates often move.
- Expected to finish
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Sep 2027
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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1 day to 1 week
- 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: * Term newborns (≥37 gestational weeks) * Without neurological disorders * Who have not undergone any painful procedure (e.g., injection, venipuncture) in the previous 24 hours * For whom heel lance for routine screening tests is planned * Whose parents provided written informed consent * Who have not received analgesic or sedative medications Exclusion Criteria: * Clinically unstable infants before or during the procedure (e.g., respiratory distress, cardiac instability) * Infants whose position was changed, intervention was interrupted, or procedure repeated in a way that could affect pain perception * Parental withdrawal of consent during the procedure * Severe restlessness or sudden physiological changes preventing pain assessment * Infants for whom standardized data could not be collected due to protocol violations
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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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ataturk University
Erzurum, Turkey (Türkiye)
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