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Comparison · NCT03026790-e87666f8

Active Comparator: Telecare Collaborative Management (TCM) vs Active Comparator: Integrated Pain Team (IPT): 50% Reduction in Opioid Daily Dose

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. Active Comparator: Telecare Collaborative Management (TCM) vs Active Comparator: Integrated Pain Team (IPT): 50% Reduction in Opioid Daily Dose. Trial comparisons, record NCT03026790-e87666f8. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03026790-e87666f8

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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 10.2530.2130.298wilson
Risk in group 20.2460.2060.29wilson
Risk difference, group 1 minus group 20.00749-0.05240.0672newcombe hybrid score
Risk ratio, group 1 over group 21.030.811.31log
Odds ratio, group 1 over group 21.040.7561.43log
Number needed to treat, for one more participant with the outcome on Active Comparator: Telecare Collaborative Management (TCM) than on Active Comparator: Integrated Pain Team (IPT)134from the risk difference intervalthe interval includes no difference

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Active Comparator: Telecare Collaborative Management (TCM)Uses medication management approach delivered by a clinical pharmacist care manager with a collaborating physician to address common barriers to effective pain medication management in primary care.102403OG000
Group 2Active Comparator: Integrated Pain Team (IPT)Uses a biopsychosocial management approach delivered by a multidisciplinary team that emphasizes non-pharmacological pain management options.98399OG001

Outcome

Type
SECONDARY
Title
50% Reduction in Opioid Daily Dose
Description
Binary response variable defined by reduction of at least 50% in opioid daily dose (morphine-equivalent mg) from baseline
Time frame
12 months
Population
All participants who were alive at 12 months

Source ClinicalTrials.gov

Trial

Title
Veterans' Pain Care Organizational Improvement Comparative Effectiveness Study
NCT number
NCT03026790
Phases
PHASE2
Conditions
Chronic Pain
Interventions
Medication management, Non-pharmacological pain management, Buprenorphine-Naloxone
Lead sponsor
University of Minnesota
Results first posted
2023-06-05

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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