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Comparison · NCT03805646-5101b1ad

No Mobile Phone-administered Triage Tool vs Mobile Phone-administered Triage Tool: Proportion of Injured Patients Who Seek Clinical Follow-up Evaluation

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. No Mobile Phone-administered Triage Tool vs Mobile Phone-administered Triage Tool: Proportion of Injured Patients Who Seek Clinical Follow-up Evaluation. Trial comparisons, record NCT03805646-5101b1ad. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03805646-5101b1ad

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.5270.4920.562wilson
Risk in group 20.650.6190.68wilson
Risk difference, group 1 minus group 2-0.123-0.169-0.0764newcombe hybrid score
Risk ratio, group 1 over group 20.8110.7470.879log
Odds ratio, group 1 over group 20.60.4940.728log
Number needed to treat, for one fewer participant with the outcome on No Mobile Phone-administered Triage Tool than on Mobile Phone-administered Triage Tool8.135.9113.1from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1No Mobile Phone-administered Triage ToolFor each hospital site: Baseline data will be collected for six months.~\*\*This extended beyond 6 months due to the COVID pandemic\*\*\*409776OG000
Group 2Mobile Phone-administered Triage Tool
For each hospital site: After the first six months of baseline data collection, the mobile phone-administered triage tool (or Mobile Phone-based Triage Tool) will be implemented for a year.~\*\*This extended beyond 1 year due to the COVID pandemic\*\*\*~Mobile Phone-based Triage Tool: The proposed intervention is a mobile phone-administered survey. Participants that have been admitted to participating hospitals for treatment of injury will be contacted by mobile phone approximately two weeks after discharge. A seven-question survey will be administered over the phone to each participant. Cross-validation with a separately administered in-person physical exam will be performed to assess the survey tool's prediction of who needs further care for treatment of their injury.
615946OG001

Outcome

Type
PRIMARY
Title
Proportion of Injured Patients Who Seek Clinical Follow-up Evaluation
Description
This will be calculated as follows: The denominator will be the number of discharged trauma patients enrolled in the study. The numerator will be the number of discharged trauma patients enrolled in the study who seek any clinical follow-up evaluation at the 2 weeks post-discharge phonecall.
Time frame
After the 2week post-discharge phonecall.
Population
There was missing data for this variable hence the discrepancy between the overall number of participants analyzed for this variable and participants in the study. Missing data were dropped from the analysis.

Source ClinicalTrials.gov

Trial

Title
Mobile Phone-administered Triage Tool to Followup on Discharged Trauma Patients
NCT number
NCT03805646
Phases
NA
Conditions
Wounds and Injury
Interventions
Mobile Phone-based Triage Tool
Lead sponsor
University of California, Los Angeles
Results first posted
2024-11-27

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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