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N/A Completed N=23,026 Other

Substudy of Protocol NCT03843957 - Effect of mPATH on Screening for Depression, Fall Risk, and Safety

Source: ClinicalTrials.gov NCT05110014 ↗
Enrolled (actual)
23,026
Serious AEs
Results posted
Apr 2022
Primary outcomePrimary: Number of Participants Screening Positive for Depression, Fall Risk or Intimate Partner Violence - Pre mPATH Use — 224; 94; 55; 165 Participants

Summary

This is a sub-study for data analysis of data collected as part of the larger randomized controlled trial "Effectiveness and Implementation of mPATH-CRC" (NCT03843957) to determine if self-administered screening with an iPad increases the detection of patients with depression, falls, and intimate partner violence.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants Screening Positive for Depression, Fall Risk or Intimate Partner Violence - Pre mPATH Use
224; 94; 55; 165; 265; 264
PRIMARY
Number of Participants Screening Positive for Depression, Fall Risk or Intimate Partner Violence - Post mPATH Use
509; 463; 235; 242; 418; 235
SECONDARY
Number of Participants Screening Positive for Depression Using Patient Health Questionnaires (PHQ-2 Score of 3 or Greater)
188; 450
SECONDARY
Number of Participants Screening Positive for Moderately Severe or Severe Depression Using Patient Health Questionnaires (PHQ-9 Score Greater Than 14)
82; 206
SECONDARY
Number of Participants Screening Positive for Severe Depression Using Patient Health Questionnaires (PHQ-9 Score Greater Than 19)
28; 86
SECONDARY
Number of Participants With a Patient Health Questionnaires (PHQ-9 Score Greater Than 14) and Not Currently Taking a Medication for Depression.
63; 139
SECONDARY
Number of Participants Who Report Thoughts of Self Harm - Patient Health Questionnaire (PHQ-9) in All Practices
39; 116
SECONDARY
Number of Participants Screening Positive for Fall Risk at Home in All Practices
907; 1692
SECONDARY
Number of Participants Screening Positive for Intimate Partner Violence in All Practices
10; 310

Eligibility Criteria

Inclusion Criteria

  • Age 18 or older
  • Completed a provider visit at the study clinic during the 60 days prior to the clinic launching the mPATH program (the "pre" time period), or completed a provider visit at the study clinic during days 14 - 73 after the launch of mPATH (the "post" time period)
  • Have a preferred language of English or Spanish

Exclusion Criteria

  • Requiring a language interpreter for a language other than Spanish
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05110014). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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