NCT07170670Completed
Cognitive-Behavioral Care for Port Needle Insertion
Cognitive-Behavioral Intervention Package for Port Catheter Needle Insertion: Effects on Pain, Anxiety, and Fear in Children With Cancer
Source: ClinicalTrials.gov · Last updated 18 Sept 2025
Brief summary (registry, in English)
This study aims to determine the effect of the Cognitive-Behavioral Intervention Package (CBIP) applied during port catheter needle insertion on pain, anxiety, and fear levels in children aged 6-18 years diagnosed with oncology. Research Hypotheses Between the Cognitive-Behavioral Intervention Package group (G1) and the control group (G2): H1: There is a difference in the mean scores of the Wong-Baker FACES Pain Rating Scale (WB-FPRS) between the groups. H2: There is a difference in the mean scores of the Children's Anxiety Scale between the groups. H3: There is a difference in the mean scores of the Children's Fear Scale between the groups. Prior to the intervention, researchers will administer the scales to the intervention group, followed by the implementation of the CBIP. After the port catheter needle insertion, the scales will be re-administered to evaluate the final levels of pain, anxiety, and fear.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 54 (actual)
- First submitted
- 19 Aug 2025
- Start date
- 16 Sept 2024
- Primary completion date
- 18 Jul 2025
- Lead sponsor
- Birgul Erdogan
- Diseases
- Childhood cancers
- NCT number
- NCT07170670
What you commit to
- Study type: Interventional
- Participants enrolled: 54
- From 16 Sept 2024 to the primary completion date, 18 Jul 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Have a history of sedative, analgesic, or narcotic use within 24 hours prior to enrollment,
Other illness
- Have any visual, auditory, verbal, or cognitive impairment,
- Are in the terminal stage of the disease,
- Have a fever or history of infection at the time of enrollment,
Other
- Have a pre-procedure WB-FPRS score of 2 or higher unrelated to the procedure,
- Do not complete the study.
Who the study is looking for
- 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.
Age in the registry: 6 years to 18 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Kocaeli University Faculty of Health Sciences Coordinator of this site? Confirm its status | İzmit | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.