Participatory Messaging in the UCLA Psychiatry Partial Hospitalization and Intensive Outpatient Programs
Primary Purpose
Depression, Anxiety, Psychosis
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Participatory technology development
Usual Care
Sponsored by
About this trial
This is an interventional treatment trial for Depression
Eligibility Criteria
Inclusion Criteria:
- Patients (over the age of 18) or parents of patients who are minors (between the ages of 6 and 17)
- Enrolled in PHP or IOP programs at Resnick Neuropsychiatric Hospital
- Agree to participate (minors will be required to have parental consent)
- Patient participants will need to be English speaking because text and IVR messages and workshops will be conducted in English.
- Patient must have cellular phone that can receive text messages
- All PHP and IOP staff are eligible and will be invited to participate in workshops and complete surveys.
Exclusion Criteria:
- Declines consent or is unwilling to participate in the study
- Does not speak English. Language other than English is an exclusion given resources and capacity of the study
- Patients without a cellular phone that can receive text messages
- Not receiving texts or IVR messages from their program is an exclusion given that it is the intervention we are evaluating
- Patients under the age of 6.
Sites / Locations
- UCLA Partial Hospitalization and Intensive Outpatient ProgramsRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Usual care
Participatory technology development
Arm Description
Control arm - these patients will get usual care as part of the PHP and IOP programs at UCLA. They will not receive mobile support messages.
Intervention - Patients will have access to a website that allows them to co-create mobile support messages with their therapist to support their care as part of the PHP and IOP programs at UCLA.
Outcomes
Primary Outcome Measures
Change in homework completion rate
the change in the degree to which patients complete tasks assigned to them by their provider as part of their treatment
Secondary Outcome Measures
length of stay
length of stay (in terms of days and hours/day of program attendance)
time to discharge
time to step down from partial hospitalization program to intensive outpatient program and time to discharge from program
Number of patient visits to health care organizations outside of clinic
the number of services that patients utilize outside of the clinic, including ED visits and inpatient hospitalizations.
Types of health care services patients utilize outside of clinic
the types of services that patients utilize outside of the clinic, including ED visits and inpatient hospitalizations.
change in depression symptoms
PHQ-9 to measure changes in depression symptoms
Change in Patient Treatment Self-Efficacy
change patient treatment self-efficacy from week-to-week during program
Difference in Patient Satisfaction with Program between Intervention vs Control groups
comparing patient satisfaction with services and support between the intervention and control groups
Messaging Application Usability
Weekly survey of patients in the intervention arm and all providers to assess the usability of the messaging application
Patient Involvement in Message Development
Completed by patients in the intervention arm and by provider for each patient in intervention arm to assess the extent of patient involvement in the development of message content and schedule, and use of messaging application
Full Information
NCT ID
NCT02708940
First Posted
February 4, 2016
Last Updated
March 9, 2016
Sponsor
University of California, Los Angeles
1. Study Identification
Unique Protocol Identification Number
NCT02708940
Brief Title
Participatory Messaging in the UCLA Psychiatry Partial Hospitalization and Intensive Outpatient Programs
Study Type
Interventional
2. Study Status
Record Verification Date
March 2016
Overall Recruitment Status
Unknown status
Study Start Date
February 2016 (undefined)
Primary Completion Date
September 2016 (Anticipated)
Study Completion Date
December 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, Los Angeles
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This research project aims to evaluate the feasibility and effectiveness of a new approach to tailored mobile applications using the Chorus Participatory Mobile Framework. PHP and IOP program participants-patients and therapists--will be consented and enrolled by study staff. Study participants will be invited to workgroups specific to their program to discuss the usability of Chorus and be asked to complete surveys on demographics, satisfaction, self-efficacy, and involvement with Chorus and usability of the tool.
Detailed Description
The Partial Hospitalization Program (PHP) and Intensive Outpatient Program (IOP) in the Neuropsychatric Hospital at UCLA provide psychiatric services for adults and children with acute mental illness. These include voluntary programs that support individuals in their recovery with the goal to assist patients in achieving the highest level of independence. Most programs operate Monday through Friday between four to eight hours a day. Recently, the PHP and IOP programs have decided to start including mobile messaging as a part of care, helping patients to feel supported even after they have left the hospital for the day.
The purpose of this study is to evaluate the feasibility and effectiveness of their ongoing use of the Chorus Participatory Mobile Framework to support clinical care. Chorus is a framework and web application that allows users to rapidly create a broad range of automated text messaging (SMS), interactive voice (IVR), or mobile web applications using a simple and accessible visual interface without requiring any server programming. There will be two broad populations using Chorus: (1) programs (e.g. OCD Intensive Treatment Program) in which all participants will receive participatory mobile messaging and (2) programs (e.g. Adult Acute PHP) in which patients will be randomized to receive either participatory mobile messaging or no mobile messaging. Across all programs, Kandace Whiting and Armen Arevian will train PHP and IOP therapists starting with creating simple, basic, useful messaging content in Chorus to support patients in achieving program goals. Examples of messages include Cognitive Behavioral Therapy (CBT), symptom management, and stress management cues to patients in the Obsessive Compulsive Disorder Clinic, patients in the Adult Eating Disorder Clinic, and parents from The Achievement, Behavior, Cognition (ABC) Child Programs.
All participating patients receiving participatory mobile messaging will work with program staff one-on-one to tailor SMS and IVR content and design based on their own preferences. By being able to personalize the messaging, the Chorus Participatory Mobile Framework meets the capacities and preferences of the users rather than a "one-size" approach requiring adaptation of the users to the technology. Both therapists and patients will be invited to up to bi-weekly, in-person workshops specific to their program to provide feedback and input. The goal of these workshops is to further develop and refine the novel mobile interventions based on stakeholder input. The Chorus Participatory Framework will be used during the workshops to develop and test the application in real-time. Workshops will be audio and/or video recorded to document the process.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Anxiety, Psychosis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Usual care
Arm Type
Active Comparator
Arm Description
Control arm - these patients will get usual care as part of the PHP and IOP programs at UCLA. They will not receive mobile support messages.
Arm Title
Participatory technology development
Arm Type
Active Comparator
Arm Description
Intervention - Patients will have access to a website that allows them to co-create mobile support messages with their therapist to support their care as part of the PHP and IOP programs at UCLA.
Intervention Type
Other
Intervention Name(s)
Participatory technology development
Intervention Description
Creating mobile support tools by patients and their therapists
Intervention Type
Other
Intervention Name(s)
Usual Care
Intervention Description
Usual care as part of the UCLA PHP and IOP programs
Primary Outcome Measure Information:
Title
Change in homework completion rate
Description
the change in the degree to which patients complete tasks assigned to them by their provider as part of their treatment
Time Frame
Collected on each program attendance day (up to daily), through discharge from program, an average of 12 weeks
Secondary Outcome Measure Information:
Title
length of stay
Description
length of stay (in terms of days and hours/day of program attendance)
Time Frame
At discharge from program, an average of 12 weeks
Title
time to discharge
Description
time to step down from partial hospitalization program to intensive outpatient program and time to discharge from program
Time Frame
From admission to program until discharge from program, assessed up to 20 weeks
Title
Number of patient visits to health care organizations outside of clinic
Description
the number of services that patients utilize outside of the clinic, including ED visits and inpatient hospitalizations.
Time Frame
at patient disenrollment from study, approximately 3 months after discharge from program, up to 40 weeks
Title
Types of health care services patients utilize outside of clinic
Description
the types of services that patients utilize outside of the clinic, including ED visits and inpatient hospitalizations.
Time Frame
at patient disenrollment from study, approximately 3 months after discharge from program, up to 40 weeks
Title
change in depression symptoms
Description
PHQ-9 to measure changes in depression symptoms
Time Frame
Upon admission to program, at mid-point of stay in program, at discharge from program (may also be up to weekly during stay), an average of 12 weeks; and 3 months after discharge from programa
Title
Change in Patient Treatment Self-Efficacy
Description
change patient treatment self-efficacy from week-to-week during program
Time Frame
weekly during stay in program, through discharge from program, an average of 12 weeks
Title
Difference in Patient Satisfaction with Program between Intervention vs Control groups
Description
comparing patient satisfaction with services and support between the intervention and control groups
Time Frame
at discharge from program, an average of 12 weeks
Title
Messaging Application Usability
Description
Weekly survey of patients in the intervention arm and all providers to assess the usability of the messaging application
Time Frame
weekly during stay in program, through discharge from program, an average of 12 weeks
Title
Patient Involvement in Message Development
Description
Completed by patients in the intervention arm and by provider for each patient in intervention arm to assess the extent of patient involvement in the development of message content and schedule, and use of messaging application
Time Frame
weekly during stay in program, through discharge from program, an average of 12 weeks
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients (over the age of 18) or parents of patients who are minors (between the ages of 6 and 17)
Enrolled in PHP or IOP programs at Resnick Neuropsychiatric Hospital
Agree to participate (minors will be required to have parental consent)
Patient participants will need to be English speaking because text and IVR messages and workshops will be conducted in English.
Patient must have cellular phone that can receive text messages
All PHP and IOP staff are eligible and will be invited to participate in workshops and complete surveys.
Exclusion Criteria:
Declines consent or is unwilling to participate in the study
Does not speak English. Language other than English is an exclusion given resources and capacity of the study
Patients without a cellular phone that can receive text messages
Not receiving texts or IVR messages from their program is an exclusion given that it is the intervention we are evaluating
Patients under the age of 6.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Armen Arevian, MD, PhD
Email
aarevian@mednet.ucla.edu
Facility Information:
Facility Name
UCLA Partial Hospitalization and Intensive Outpatient Programs
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Armen Arevian, MD, PhD
Email
aarevian@mednet.ucla.edu
First Name & Middle Initial & Last Name & Degree
Armen Arevian, MD, PhD
First Name & Middle Initial & Last Name & Degree
James Rosser, LCSW
First Name & Middle Initial & Last Name & Degree
Jennifer O'Hora, PhD
First Name & Middle Initial & Last Name & Degree
Kandace Kelley, RN
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Participatory Messaging in the UCLA Psychiatry Partial Hospitalization and Intensive Outpatient Programs
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