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Understanding the Efficacy of Mobile Apps as Intervention for Depression in Adults When Deployed as Part of Primary Care.

Not Applicable
Completed
Conditions
Depression
Primary Health Care
Anxiety
Interventions
Behavioral: IntelliCare
Registration Number
NCT03500536
Lead Sponsor
Actualize Therapy
Brief Summary

The clinical study is meant to optimize the mobile intervention, to develop a robust implementation plan for the mobile intervention within primary care, and to conduct an effectiveness trial, randomizing 128 participants in order to understand effect on severity of depression and anxiety symptoms, cost-effectiveness, and usability of mobile apps.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
146
Inclusion Criteria
  • Positive screen on PHQ-9
Exclusion Criteria
  • Does not own or use a mobile smart phone

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
ExperimentalIntelliCare8 weeks of IntelliCare treatment followed by 8 weeks of treatment as usual.
Primary Outcome Measures
NameTimeMethod
Symptoms of depression8 weeks

Using the PHQ-9 screener

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Arkansas for Medical Sciences

🇺🇸

Little Rock, Arkansas, United States

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