Menu
Recruiting NCT07234396

Animated Video and Associated Pain and Anxiety Reduction, Following Pin Removal Post-supracondylar Fracture Fixation

No phase Interventional Supracondylar Fractures Fracture Fixation Pain Severity Anxiety

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: K-wire removal with animated procedure video being shown to the patient during its performance., K-wire removal without animated procedure video being shown to the patient during its performance..
Who it may be relevant to
Registry conditions: Supracondylar Fractures, Fracture Fixation, Pain Severity, Anxiety. Basic parameters: 4 years — 12 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Pakistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Animated Procedure Video Reduces Pain and Anxiety Among Pediatric Patients Undergoing Pin Removal Following Supracondylar Fracture Fixation - A Randomized Controlled Trial

Overview

Assessing the reduction in pain and anxiety by the use of showing an animated video of the procedure, among pediatric patients undergoing pin removal after fixation of supracondylar fractures.

Detailed description

Supracondylar fractures requiring K-wire fixation ultimately undergo pin removal after fracture fixation. This is a cause of pain and anxiety to children. This study aims to curtail the aforementioned troubles by distracting the patient using an animated video of the procedure. Patients will be randomized into two arms, and pain and anxiety scales will be implemented before, during, and after the procedure to assess whether a change exists between the two arms.

Interventions

  • Procedure K-wire removal with animated procedure video being shown to the patient during its performance.
    K-wire removal, post-supracondylar fracture fixation, will be performed while showing the patient an animated video of the procedure.
  • Procedure K-wire removal without animated procedure video being shown to the patient during its performance.
    K-wire removal, post-supracondylar fracture fixation, will be performed without showing the patient an animated video of the procedure.

Primary outcome measures

  • Wong Baker Pain scale (WBS) [Time frame: Evaluation will be done as per the criteria before, during the standard procedure, and 60 minutes post-procedure.]
  • Children's Hospital of Eastern Ontario Pain Scale (CHEOPS) [Time frame: Evaluation will be done as per the criteria before, during the standard procedure, and 60 minutes post-procedure.]
  • Children's Anxiety Meter-State (CAM-S) [Time frame: Evaluation will be done as per the criteria before, during the standard procedure, and 60 minutes post-procedure.]
  • Short State Trait Anxiety Inventory Scale (STAI) [Time frame: Evaluation will be done as per the criteria before, during the standard procedure, and 60 minutes post-procedure.]

Eligibility criteria

Inclusion criteria

  • Patients with supracondylar fractures operated on for percutaneous K-wire fixation.
  • Age between 4 to 12 years

Exclusion criteria

  • Any syndromic patients
  • Patients having any visual or cognitive disability
  • Patients having any pre-operative or post-operative complications before pin removal.
  • Patients undergoing the procedure under general anesthesia.
  • Age <4 or >12

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Quadruple blind
Primary purpose
Supportive care

Study locations

Pakistan · 1 center
  • Liaquat National Hospital — Karachi

Identifiers

NCT: NCT07234396 · RC-LNH-Orthopedics-10/2025/126

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗