Baseline (Duke) vs Post Comfort Talk® Training: Oral Sedation Rate (Duke)
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.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note | Source |
|---|---|---|---|---|---|---|
| Risk in group 1 | 0.0247 | 0.0203 | 0.0299 | wilson | ClinicalTrials.gov | |
| Risk in group 2 | 0.0144 | 0.0121 | 0.0171 | wilson | ClinicalTrials.gov | |
| Risk difference, group 1 minus group 2 | 0.0103 | 0.00515 | 0.016 | newcombe hybrid score | ClinicalTrials.gov | |
| Risk ratio, group 1 over group 2 | 1.71 | 1.32 | 2.22 | log | ClinicalTrials.gov | |
| Odds ratio, group 1 over group 2 | 1.73 | 1.33 | 2.25 | log | ClinicalTrials.gov | |
| Number needed to treat, for one more participant with the outcome on Baseline (Duke) than on Post Comfort Talk® Training | 97.4 | 62.5 | 194 | from the risk difference interval | ClinicalTrials.gov |
Groups 2
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 | Source |
|---|---|---|---|---|---|---|
| Group 1 | Baseline (Duke) | Patients who show for their MRI scans prior to team Training in Comfort Talk® | 100 | 4,051 | OG000 | ClinicalTrials.gov |
| Group 2 | Post Comfort Talk® Training | Patient who show for their MRI scans after team training in Comfort Talk® | 128 | 8,879 | OG001 | ClinicalTrials.gov |
Outcome 5
| Field | Value | Source |
|---|---|---|
| Type | SECONDARY | ClinicalTrials.gov |
| Title | Oral Sedation Rate (Duke) | ClinicalTrials.gov |
| Description | Patients who receive medical sedation on site | ClinicalTrials.gov |
| Time frame | 9 months (3 months baseline, 6 months post training) | ClinicalTrials.gov |
| Population | Patients showing for their MRI scans | ClinicalTrials.gov |
Trial 8
| Field | Value | Source |
|---|---|---|
| Title | Comfort Talk and Economic Outcomes in MRI | ClinicalTrials.gov |
| NCT number | NCT02427737 | ClinicalTrials.gov |
| Phases | NA | ClinicalTrials.gov |
| Conditions | Claustrophobia, Complication of Diagnostic Procedure | ClinicalTrials.gov |
| Interventions | Comfort Talk® Training | ClinicalTrials.gov |
| Lead sponsor | Hypnalgesics, LLC | ClinicalTrials.gov |
| Results first posted | 2019-09-12 | ClinicalTrials.gov |
| Results on ClinicalTrials.gov | https://clinicaltrials.gov/study/NCT02427737?tab=results | ClinicalTrials.gov |
Source 4
| Field | Value | Source |
|---|---|---|
| Release | trial-comparisons-2026-03-23-0.1.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57 | ClinicalTrials.gov |
| AACT copy | 2026-03-23 | ClinicalTrials.gov |
| 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 | ClinicalTrials.gov |
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.