Comparison · NCT05110014-a8f66742
Primary Care Office Visits (Pre Intervention) vs Primary Care Office Visits (Post Intervention): Number of Participants Screening Positive for Intimate Partner Violence in All Practices
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. Primary Care Office Visits (Pre Intervention) vs Primary Care Office Visits (Post Intervention): Number of Participants Screening Positive for Intimate Partner Violence in All Practices. Trial comparisons, record NCT05110014-a8f66742. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05110014-a8f66742
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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 | 0.00937 | 0.0051 | 0.0172 | wilson | |
| Risk in group 2 | 0.147 | 0.133 | 0.163 | wilson | |
| Risk difference, group 1 minus group 2 | -0.138 | -0.154 | -0.122 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.0635 | 0.034 | 0.119 | log | |
| Odds ratio, group 1 over group 2 | 0.0547 | 0.029 | 0.103 | log | |
| Number needed to treat, for one fewer participant with the outcome on Primary Care Office Visits (Pre Intervention) than on Primary Care Office Visits (Post Intervention) | 7.24 | 6.47 | 8.22 | 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 | Primary Care Office Visits (Pre Intervention) | The limited use dataset will contain the following data elements for each completed patient visit:~* Date of clinic visit (where each date is indicated by a number relative to the clinic's Launch Date)~* Clinic (designated by a unique study clinic identifier)~* Type of visit completed (for example, new patient visit, return patient visit, annual exam)~* Patient age~* Patient gender~* Patient race/ethnicity~* Patient primary insurance~* Nursing staff who roomed the patient (designated by a unique study identifier)~* Whether patient used mPATH-CheckIn program (Y/N)~* Whether nursing staff used mPATH Nursing Module to transmit mPATH data to electronic health record (Y/N)~* Whether patient has a diagnosis of depression in the problem list in the EHR (Y/N)~* Whether patient has an antidepressant medication listed in the active medication list ( (Y/N)~* Results of depression screening items~* Results of fall risk screening items~* Results of safety at home screening items~Primary Care Office Visits: mPATH iPad program that contains self-administered screening items for depression, fall risk, and intimate partner violence | 10 | 1,067 | OG000 |
| Group 2 | Primary Care Office Visits (Post Intervention) | The limited use dataset will contain the following data elements for each completed patient visit:~* Date of clinic visit (where each date is indicated by a number relative to the clinic's Launch Date)~* Clinic (designated by a unique study clinic identifier)~* Type of visit completed (for example, new patient visit, return patient visit, annual exam)~* Patient age~* Patient gender~* Patient race/ethnicity~* Patient primary insurance~* Nursing staff who roomed the patient (designated by a unique study identifier)~* Whether patient used mPATH-CheckIn program (Y/N)~* Whether nursing staff used mPATH Nursing Module to transmit mPATH data to electronic health record (Y/N)~* Whether patient has a diagnosis of depression in the problem list in the EHR (Y/N)~* Whether patient has an antidepressant medication listed in the active medication list ( (Y/N)~* Results of depression screening items~* Results of fall risk screening items~* Results of safety at home screening items~Primary Care Office Visits: mPATH iPad program that contains self-administered screening items for depression, fall risk, and intimate partner violence | 310 | 2,102 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants Screening Positive for Intimate Partner Violence in All Practices
- Description
- Screen positive for safety concerns at home. In addition, the outcome below will be assessed:~* Report that conflicts turn into fights
- Time frame
- 2 months before and 2 months after using intervention
- Population
- The number includes the actual number of participants that were analyzed (2 months before and 2 months after the intervention) out of the total of participants.
Source ClinicalTrials.gov
Trial
- Title
- Substudy of Protocol NCT03843957 - Effect of mPATH on Screening for Depression, Fall Risk, and Safety
- NCT number
- NCT05110014
- Phases
- NA
- Conditions
- Depression
- Interventions
- Primary Care Office Visits
- Lead sponsor
- Wake Forest University Health Sciences
- Results first posted
- 2022-04-05
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT05110014?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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