Comparison · NCT03875339-768b31af
Navigator Arm vs Non-Intervention Arm: Number of Participants Who do Not Receive Diagnostic Audiological Testing (Aim 1)
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. Navigator Arm vs Non-Intervention Arm: Number of Participants Who do Not Receive Diagnostic Audiological Testing (Aim 1). Trial comparisons, record NCT03875339-768b31af. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03875339-768b31af
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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 | 0.236 | 0.216 | 0.258 | wilson | |
| Risk in group 2 | 0.306 | 0.279 | 0.334 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0699 | -0.104 | -0.0358 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.772 | 0.681 | 0.875 | log | |
| Odds ratio, group 1 over group 2 | 0.701 | 0.59 | 0.833 | log | |
| Number needed to treat, for one fewer participant with the outcome on Navigator Arm than on Non-Intervention Arm | 14.3 | 9.59 | 27.9 | from the risk difference interval |
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 | Navigator Arm | Examination of adherence to follow-up with a navigator.~Navigator Guidance: Use of a dedicated Navigator to determine if follow-up and compliance rates can be improved for those infants initially demonstrating an abnormal hearing result. | 378 | 1,601 | OG000 |
| Group 2 | Non-Intervention Arm | Examination of adherence to follow-up without a navigator. | 336 | 1,098 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- PRIMARY
- Title
- Number of Participants Who do Not Receive Diagnostic Audiological Testing (Aim 1)
- Description
This outcome is the number of participants who do not follow-up at an OCSHCN Clinic for diagnostic audiologic testing after a failed newborn hearing screening from the date of randomization to 3 months after birth.
- Time frame
- 3 months. (This is the amount of time from an abnormal screen at birth to an expected follow-up at a clinic or hospital.)
- Population
Source ClinicalTrials.gov
Trial
- Title
- Communities Helping the Hearing of Infants by Reaching Parents
- NCT number
- NCT03875339
- Phases
- NA
- Conditions
- Congenital Hearing Loss
- Interventions
- Navigator Guidance
- Lead sponsor
- Matthew Bush, MD
- Results first posted
- 2025-02-14
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03875339?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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