New distraction technique may ease needle pain for kids with cancer
NCT ID NCT07170670
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested a cognitive-behavioral intervention package (CBIP) in 54 children aged 6-18 with cancer who needed a port catheter needle insertion. The package included distraction, guidance, and parental support before and during the procedure. Researchers measured pain, anxiety, and fear levels before and after the insertion to see if the intervention helped.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Cognitive-Behavioral Intervention Package (CBIP) - a combination of distraction, guidance, and parental support
- What this could lead to
- If effective, this approach could offer a simple, drug-free way to make port needle insertions less painful and scary for children with cancer.
- What could go wrong
- This is a small, completed study with only 54 participants. The results may not apply to all children, and the intervention depends on the skill of the researcher.
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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54 people
The number who actually took part.
- Started
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Sep 2024
- Finished
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Aug 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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6 to 18 years
- 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: * Are 6-18 years old, * Have a cancer diagnosis, * Have undergone at least one prior port catheter needle insertion, * Are willing to participate along with parental consent. Exclusion Criteria: * Have any visual, auditory, verbal, or cognitive impairment, * Are in the terminal stage of the disease, * Have a history of sedative, analgesic, or narcotic use within 24 hours prior to enrollment, * Have a fever or history of infection at the time of enrollment, * Have a pre-procedure WB-FPRS score of 2 or higher unrelated to the procedure, * Do not complete the study.
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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
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Kocaeli University Faculty of Health Sciences
İzmit, Kocaeli, Turkey (Türkiye)
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