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

A

Actualize Therapy

Status

Completed

Conditions

Primary Health Care
Depression
Anxiety

Treatments

Behavioral: IntelliCare

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

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.

Enrollment

146 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Positive screen on PHQ-9

Exclusion criteria

  • Does not own or use a mobile smart phone

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

146 participants in 2 patient groups

Waitlist Control
No Intervention group
Description:
8 weeks of treatment as usual followed by 8 weeks of IntelliCare treatment.
Experimental
Experimental group
Description:
8 weeks of IntelliCare treatment followed by 8 weeks of treatment as usual.
Treatment:
Behavioral: IntelliCare

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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