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EHR-facilitated Collaborative Care (Intervention) vs Usual Care (Control): Number of Deceased Participants

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

Measures 6

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

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.1280.1240.133wilsonClinicalTrials.gov
Risk in group 20.1370.1320.142wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00851-0.0153-0.00181newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.9380.8920.986logClinicalTrials.gov
Odds ratio, group 1 over group 20.9290.8760.984logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on EHR-facilitated Collaborative Care (Intervention) than on Usual Care (Control)11865.5553from the risk difference intervalClinicalTrials.gov

Groups 2

Group 2 names the comparator: usual care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1EHR-facilitated Collaborative Care (Intervention)
Participants were administered ePROMs during EHR-facilitated collaborative care (ECC) periods. Automated responses, matched to symptom type and intensity, appeared following a patient's report of an actionable symptom, defined as \>=4/10 on a numeric rating scale (NRS). For any actionable symptom, respondents were asked if they wanted to receive symptom-specific self-management resources. For severe symptoms, \>=7/10, respondents were asked if they wanted to work remotely with a Symptom Care Manager (SCM) to develop an individualized symptom management plan.
3,19224,874OG001ClinicalTrials.gov
Group 2Usual Care (Control)Participants were administered ePROM surveillance alone.2,21416,180OG000ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of Deceased ParticipantsClinicalTrials.gov
DescriptionVital status (living or deceased) was determined by Accurint record search across multiple sources, including the Social Security Death IndexClinicalTrials.gov
Time frameUp to 46 months (beginning from a participants' index medical oncology encounter until death or end of study)ClinicalTrials.gov
PopulationClinicalTrials.gov

Trial 8

FieldValueSource
TitleEnhanced, EHR-facilitated Cancer Symptom Control Pragmatic Clinical TrialClinicalTrials.gov
NCT numberNCT03892967ClinicalTrials.gov
PhasesNAClinicalTrials.gov
ConditionsHematopoietic and Lymphoid Cell Neoplasm, Malignant Solid NeoplasmClinicalTrials.gov
InterventionsInterview, Quality-of-Life Assessment, Questionnaire AdministrationClinicalTrials.gov
Lead sponsorMayo ClinicClinicalTrials.gov
Results first posted2025-10-07ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT03892967?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.