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Effect of Patterned Versus Plain Fixation on Pain During IV Therapy in Children

The Effect of Patterned Versus Plain Fixation Materials on Pain and Physiological Parameters in Children Receiving Intravenous Therapy: A Randomized Two-Period Crossover Trial

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07316036
Acronym
P-FLACC
Enrollment
40
Registered
2026-01-05
Start date
2025-04-01
Completion date
2026-01-30
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intravenous Therapy, Kronik hastalık, Pain

Keywords

çocuklarda ağrı, desenli tespit malzemesi, non farmakolojik yöntemler, fizyolojik parametreler, ağrı puanı

Brief summary

The goal of this clinical trial is to learn whether using patterned fixation materials during intravenous therapy can reduce pain and affect physiological responses in children. Children who regularly receive intravenous therapy will take part in this study. Each participant will receive both patterned and plain fixation materials on different treatment days. Pain levels will be measured using an observation-based pain scale, and oxygen saturation and pulse rate will be recorded before and after the procedure.

Detailed description

This study is a randomized two-period crossover clinical trial designed to examine whether patterned fixation materials used during intravenous (IV) catheter placement reduce pain and influence physiological responses in children. The trial focuses on children who regularly receive IV therapy for chronic conditions and aims to compare two commonly used fixation materials: patterned fixation tape and plain fixation tape. Participants are randomly assigned to one of two sequences. In Sequence AB, children receive the patterned fixation material during their first IV procedure and the plain fixation material during their next scheduled IV procedure. In Sequence BA, children receive the plain fixation material first and the patterned fixation material during their next procedure. A washout period of at least one week naturally occurs between visits because children attend the day treatment unit weekly or every three weeks for routine therapy. This interval is considered sufficient to prevent carry-over effects, as the intervention is a short-term non-pharmacological distraction method. During each IV procedure, pain is assessed using the FLACC behavioral pain scale by two independent observers, and physiological parameters (oxygen saturation and pulse rate) are measured one minute before and one minute after the procedure. Each child serves as their own control, allowing within-participant comparisons between the patterned and plain fixation conditions. The primary objective of the study is to determine whether patterned fixation materials lower pain scores compared with plain fixation materials. Secondary objectives include examining whether patterned fixation materials lead to more favorable physiological responses during IV catheter insertion.

Interventions

DEVICEPatterned fixation tape

Patterned fixation tape is applied to secure the intravenous catheter after insertion, with the patterned surface remaining visible to the child during the procedure.

DEVICEPlain fixation tape

Plain fixation tape is applied to secure the intravenous catheter after insertion using standard, non-patterned fixation materials.

Sponsors

Necmettin Erbakan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

No masking was applied because the intervention involved visibly different fixation materials (patterned versus plain), making blinding of participants and healthcare providers not feasible.

Intervention model description

This study uses a two-period randomized crossover design. Participants are assigned to one of two sequences (patterned fixation first, then plain; or plain fixation first, then patterned). Each child receives both interventions on different treatment days, serving as their own control.

Eligibility

Sex/Gender
ALL
Age
3 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

- Children aged between 3 and 12 years * Children who regularly receive intravenous therapy for chronic conditions * Ability of the child and parent/legal guardian to understand the study procedures * Written informed consent obtained from the parent or legal guardian * Assent obtained from the child when appropriate

Exclusion criteria

* \- Presence of acute pain at the time of the procedure * Diagnosis of conditions that may interfere with pain assessment, such as cerebral palsy or neuromuscular or peripheral nervous system disorders * Requirement for more than one intravenous catheter insertion attempt during the procedure * Withdrawal of consent by the child or parent/legal guardian

Design outcomes

Primary

MeasureTime frameDescription
Pain intensityImmediately after intravenous fixation during each study periodPain intensity was assessed using the FLACC (Face, Legs, Activity, Cry, Consolability) observational pain scale. The total score ranges from 0 to 10, with higher scores indicating more severe pain.

Secondary

MeasureTime frameDescription
Physiological parameters, Spo2Immediately before and immediately after each intervention periodOxygen saturation (SpO₂) measured before and after intravenous fixation.
Physiological parameters, heart rateImmediately before and immediately after each intervention periodheart rate measured before and after intravenous fixation.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026