Gentle massage may ease stomach troubles for Ventilator-Dependent children
NCT ID NCT04841174
First seen Jun 27, 2026 · Last updated Aug 27, 2026 · Updated 2 times
Summary
This study tested whether gentle abdominal massage could reduce common stomach problems like vomiting, bloating, and poor digestion in children aged 1 to 24 months who are on breathing machines and feeding tubes in the pediatric ICU. Nurses gave the massage and tracked things like stomach residue, bowel sounds, and vomiting. The goal is to find a simple, drug-free way to help these fragile kids tolerate their feedings better.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- abdominal massage
- What this could lead to
- If it works, this simple, low-cost technique could help reduce stomach problems in critically ill children on feeding tubes, potentially improving nutrition and shortening hospital stays.
- What could go wrong
- This is a very small, early study with only 24 children. Results may not apply to all patients, and the effect of massage may be minimal or hard to measure in a busy ICU setting.
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
-
24 people
The number who actually took part.
- Started
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Mar 2021
- Finished
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Jan 2023
- Lead sponsor
-
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
-
1 month to 24 months
- Sex
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Anyone
- Healthy volunteers
-
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: Obtaining parental permission and a signed informed voluntary consent form; the child being aged between 1 and 24 months; receiving mechanical ventilation support for at least 48 hours and being endotracheally intubated; receiving full enteral nutrition during this period; being fed via a nasogastric/orogastric tube and receiving the same type of enteral formula; and receiving sedation. Exclusion criteria: A high (15%-30%) or very high (\>30%) expected mortality rate according to the PRISM III (Pediatric Risk of Mortality) score; planned extubation; lack of anatomical integrity of the gastrointestinal system (history of abdominal surgery, presence of gastrostomy or stoma, presence of tracheostomy); hemodynamic instability; and the presence of severe neurological conditions such as intracranial hemorrhage, increased intracranial pressure, or cranial tumors.
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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
-
Bakırkoy Dr. Sadi Konuk Training and Research Hospital
Bakırköy, Istanbul, Turkey (Türkiye)
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