Depression Clinical Trial
Verified date | November 2023 |
Source | University of California, Los Angeles |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 150 |
Est. completion date | December 2016 |
Est. primary completion date | September 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
United States | UCLA Partial Hospitalization and Intensive Outpatient Programs | Los Angeles | California |
Lead Sponsor | Collaborator |
---|---|
University of California, Los Angeles |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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 | Collected on each program attendance day (up to daily), through discharge from program, an average of 12 weeks | |
Secondary | length of stay | length of stay (in terms of days and hours/day of program attendance) | At discharge from program, an average of 12 weeks | |
Secondary | time to discharge | time to step down from partial hospitalization program to intensive outpatient program and time to discharge from program | From admission to program until discharge from program, assessed up to 20 weeks | |
Secondary | 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. | at patient disenrollment from study, approximately 3 months after discharge from program, up to 40 weeks | |
Secondary | 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. | at patient disenrollment from study, approximately 3 months after discharge from program, up to 40 weeks | |
Secondary | change in depression symptoms | PHQ-9 to measure changes in depression symptoms | 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 | |
Secondary | Change in Patient Treatment Self-Efficacy | change patient treatment self-efficacy from week-to-week during program | weekly during stay in program, through discharge from program, an average of 12 weeks | |
Secondary | Difference in Patient Satisfaction with Program between Intervention vs Control groups | comparing patient satisfaction with services and support between the intervention and control groups | at discharge from program, an average of 12 weeks | |
Secondary | Messaging Application Usability | Weekly survey of patients in the intervention arm and all providers to assess the usability of the messaging application | weekly during stay in program, through discharge from program, an average of 12 weeks | |
Secondary | 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 | weekly during stay in program, through discharge from program, an average of 12 weeks |
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