New distraction technique may ease needle pain for kids with cancer

NCT ID NCT07170670

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

54 people

The number who actually took part.

Started

Sep 2024

Finished

Aug 2025

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

6 to 18 years

Sex

Anyone

Healthy volunteers

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

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.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Cancer are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

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

  • Kocaeli University Faculty of Health Sciences

    İzmit, Kocaeli, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.