Comparison · NCT03026790-sae
Active Comparator: Telecare Collaborative Management (TCM) vs Active Comparator: Integrated Pain Team (IPT): serious adverse events
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Active Comparator: Telecare Collaborative Management (TCM) vs Active Comparator: Integrated Pain Team (IPT): serious adverse events. Trial comparisons, record NCT03026790-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03026790-sae
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.304 | 0.259 | 0.354 | wilson | |
| Risk in group 2 | 0.3 | 0.255 | 0.349 | wilson | |
| Risk difference, group 1 minus group 2 | 0.00419 | -0.0626 | 0.071 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.01 | 0.812 | 1.27 | log | |
| Odds ratio, group 1 over group 2 | 1.02 | 0.742 | 1.4 | log | |
| Number needed to harm, for one more participant with a serious adverse event on Active Comparator: Telecare Collaborative Management (TCM) than on Active Comparator: Integrated Pain Team (IPT) | 238 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Active 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. | 109 | 358 | EG000 |
| Group 2 | Active Comparator: Integrated Pain Team (IPT) | Uses a biopsychosocial management approach delivered by a multidisciplinary team that emphasizes non-pharmacological pain management options. | 109 | 363 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- 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
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03026790?tab=results
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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