Comparison · NCT02056431-600e9dca
IVR Control Group vs IVR Intervention Group: Number of Participants With Minimally Effective Dose in 12 Months
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. IVR Control Group vs IVR Intervention Group: Number of Participants With Minimally Effective Dose in 12 Months. Trial comparisons, record NCT02056431-600e9dca. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02056431-600e9dca
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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 | 0.484 | 0.445 | 0.523 | wilson | |
| Risk in group 2 | 0.517 | 0.476 | 0.558 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0331 | -0.0899 | 0.024 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.936 | 0.835 | 1.05 | log | |
| Odds ratio, group 1 over group 2 | 0.876 | 0.697 | 1.1 | log | |
| Number needed to treat, for one fewer participant with the outcome on IVR Control Group than on IVR Intervention Group | 30.2 | 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 | IVR Control Group | Participants will receive 3 non-interactive voice response (IVR) calls (2nd, 4th,and 6th months post start date) containing generic messages regarding diabetes education | 299 | 618 | OG000 |
| Group 2 | IVR Intervention Group | Participants will receive 3 interactive voice response (IVR) calls (2nd, 4th,and 6th months post start date) to collect information on medication use, side effects, rating of side effects and pain symptoms to be fed back to their physicians | 290 | 561 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants With Minimally Effective Dose in 12 Months
- Description
- Count of patients who ever received a minimally effective dose of the medications they started on during the 12 months following treatment start (measured post only).
- Time frame
- 12 months
- Population
- 1179 Patient completed the close out survey
Source ClinicalTrials.gov
Trial
- Title
- Balancing Treatment Outcomes and Medication Burden Among Patients With Symptomatic Diabetic Peripheral Neuropathy
- NCT number
- NCT02056431
- Phases
- NA
- Conditions
- Diabetic Peripheral Neuropathy
- Interventions
- IVR Intervention Group
- Lead sponsor
- Kaiser Permanente
- Results first posted
- 2018-02-12
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02056431?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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