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N/A Completed N=139

An Evaluation of Innerview™, a Web-based Tool to Support the Integration of Mental Health in the Primary Care Setting

Source: ClinicalTrials.gov NCT02025647 ↗
Enrolled (actual)
139
Serious AEs
0.0%
Results posted
Oct 2015
Primary outcomePrimary: Accuracy of the Narrative Module — 139 participants

Summary

Innerview can address some of the challenges of integrating mental health and primary care by accurately and reliably collecting mental health evidence and activities directly from patients, and then organizing and automating that evidence and activity into reports for providers and care teams that support diagnosis, treatment planning and monitoring of the mental health issues within a practice population.

Outcome Measures

OutcomeResultp-value
PRIMARY
Accuracy of the Narrative Module
139
PRIMARY
Reliability of the Narrative Module
94
PRIMARY
Standard Error of Measure for the Individualized Rating Scale (Rating Module)
.9
SECONDARY
Provider Survey (Question 1)
4.5
SECONDARY
Provider Survey (Question 2)
4.3
SECONDARY
Provider Survey (Question 3)
4.3
SECONDARY
Provider Survey (Question 4)
4.3
SECONDARY
Provider Survey (Question 5)
3.5
SECONDARY
Provider Survey (Question 6)
3.7
SECONDARY
Provider Survey (Question 7)
4.2
SECONDARY
Provider Survey (Question 8)
4.2
SECONDARY
Provider Survey (Question 9)
3.2
SECONDARY
Provider Survey (Question 10)
3.5
SECONDARY
Provider Survey (Question 11)
15
SECONDARY
Subject Survey (Question 1)
4.03
SECONDARY
Subject Survey (Question 2)
3.89
SECONDARY
Subject Survey (Question 3)
3.89
SECONDARY
Subject Survey (Question 4)
4.39
SECONDARY
Subject Survey (Question 5)
4.44
SECONDARY
Subject Survey (Question 6)
4.25
SECONDARY
Subject Survey (Question 7)
4.10
SECONDARY
Subject Survey (Question 8)
3.81
SECONDARY
Subject Survey (Question 9)
3.95
SECONDARY
Subject Survey (Question 10)
4.11

Eligibility Criteria

Inclusion Criteria

  • In order to be eligible to participate in this study, a subject must meet all of the following criteria:
  • Provide signed and dated informed consent form
  • Be aged 18 or older
  • Be willing to comply with all study procedures and be available for the duration of the study
  • Be able to read English at an 8th grade level (as determined by physician)
  • Have internet access to email with a computer and/or tablet

Exclusion Criteria

  • Patients are excluded from study participation if they meet any of the following criteria:
  • Inability to provide consent due to guardianship issues
  • Currently experiencing psychotic symptoms (as determined by physician)
  • Anything that, in the opinion of the Investigator, would preclude the subject's full compliance with or completion of the study.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02025647). 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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