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Comparison · NCT05110014-99fc5aa0

Primary Care Office Visits (Pre Intervention) vs Primary Care Office Visits (Post Intervention): Number of Participants Screening Positive for Fall Risk at Home 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 Fall Risk at Home in All Practices. Trial comparisons, record NCT05110014-99fc5aa0. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05110014-99fc5aa0

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.850.8270.87wilson
Risk in group 20.8050.7870.821wilson
Risk difference, group 1 minus group 20.04510.01710.0718newcombe hybrid score
Risk ratio, group 1 over group 21.061.021.09log
Odds ratio, group 1 over group 21.371.121.68log
Number needed to treat, for one more participant with the outcome on Primary Care Office Visits (Pre Intervention) than on Primary Care Office Visits (Post Intervention)22.213.958.4from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Primary 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
9071,067OG000
Group 2Primary 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
1,6922,102OG001

Outcome

Type
SECONDARY
Title
Number of Participants Screening Positive for Fall Risk at Home in All Practices
Description
Screen positive for fall risk at home. In addition, the outcomes below will be assessed:~* Have fallen in last 6 months~* Have had a fall with injury
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

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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