N/A
Completed N=320
Evaluating an eHealth Solution for Screening in Pediatric Care
Postoperative Pain · Stress Disorders, Post-Traumatic
Source: ClinicalTrials.gov NCT04506294 ↗
Enrolled (actual)
320
Serious AEs
0.0%
Results posted
Jun 2024
Primary outcomePrimary: Validity of eScreen Pain Measure as Predictor of Child's Clinically Significant Pain Severity at 6 Weeks
Summary
This study will evaluate the predictive validity of a game-based screening system based on child self-report measures.
The core study hypotheses are that (1) in-game assessments will predict problematic recovery (child pain and posttraumatic stress symptoms [PTSS]) and (2) parents in the intervention group will report greater confidence in managing child recovery.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Validity of eScreen Pain Measure as Predictor of Child's Clinically Significant Pain Severity at 6 Weeks |
— | — |
| PRIMARY Validity of eScreen Pain Measure as Predictor of Child's Clinically Significant Pain Interference at 6 Weeks |
.756 | — |
| PRIMARY Validity of eScreen Posttraumatic Stress Screen as Predictor of Posttraumatic Stress at 6 Weeks |
.822 | — |
| PRIMARY Validity of eScreen PTSS Screener as Predictor of Impairment From Posttraumatic Stress Symptoms at 6 Weeks |
.691 | — |
| SECONDARY Impact of eScreen System on Parent Confidence in Managing Child Symptoms and Recovery |
39.6; 38.9 | .536 |
Eligibility Criteria
Inclusion Criteria
- Child treated or admitted for injury or illness event that occurred within the past month
- Child has regular access to a compatible (IOS or Android) tablet at home
- Parent has an internet-capable smartphone and can receive text messages on that phone, OR has email account that can receive messages about child status
- Child and parent read or understand English well enough to consent / assent to participation and complete study tasks (e.g., checklists, use of screening system)
Exclusion Criteria
- Index medical event is due to family violence
Data sourced from ClinicalTrials.gov (NCT04506294). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.