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Clinical Trials/NCT03062267
NCT03062267
Completed
Not Applicable

Effectiveness of a Mobile Texting Intervention for People With Serious Mental Illness

University of Washington2 sites in 1 country49 target enrollmentOctober 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Schizoaffective Disorder
Sponsor
University of Washington
Enrollment
49
Locations
2
Primary Endpoint
Psychiatric Symptoms
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Testing an mHealth mobile interventionist texting program on illness management.

Detailed Description

The ultimate objective is to evaluate a validated mHealth intervention that can be realistically integrated into community mental health settings to increase the availability, reach, and broad impact of illness management approaches for people with serious mental illness (SMI).

Registry
clinicaltrials.gov
Start Date
October 1, 2017
End Date
May 31, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dror Ben-Zeev

Professor, School of Medicine: Psychiatry and Behavioral Sciences

University of Washington

Eligibility Criteria

Inclusion Criteria

  • Chart diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder, or major depressive disorder;
  • 18 years or older;
  • A rating of "3" or higher on one of three Patient Activation items;
  • Ownership of a mobile phone with call/text plan (research staff will offer assistance in accessing the Federal Lifeline Assistance Program to people who do not have a mobile phone and/or call/text plan if they are otherwise eligible);
  • Receiving community based treatment services.

Exclusion Criteria

  • Hearing, vision, or motor impairment that make it impossible to operate a mobile phone (determined using the individual's device for screening);
  • English reading level below 4th grade (determined using the reading section from the Wide Range Achievement Test - 4th Edition (WRAT-4).

Outcomes

Primary Outcomes

Psychiatric Symptoms

Time Frame: Change from baseline to 3 months and 6 months

Assessed with the Beck Depression Inventory (BDI). The Beck Depression Inventory is a psychometric test for measuring the severity of depression. There are 21 items, each rated from 0-3, and total scores range from 0-63. Higher scores indicate more severe depressive symptoms.

Secondary Outcomes

  • Recovery(Change from baseline to 3 months and 6 months)

Study Sites (2)

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