- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01749124
My Coach Connect: An Automated Telephone-based Reporting System for Patients With Mental Illness (MCC)
May 16, 2017 updated by: RAND
"My Coach Connect": Pilot Under the Partnered Research Center for Quality Care, RHINO 2008-0132
This is a pilot study for a novel, automated telephone system called "My Coach Connect".
The purpose of the study is to evaluate the feasibility and effectiveness of this telephone tool while engaging clients and providers in discussion groups and surveys to better understand how this tool impacts the care provided and their overall experience in healthcare.
Study Overview
Status
Unknown
Intervention / Treatment
Detailed Description
Clients will use this tool (My Coach Connect) to leave voice messages and survey answers which their providers will have access to by logging in to a secure website.
Providers will also be able to indicate using the website whether they found a particular narrative helpful or not.
Providers will have access to audio recordings of the voice responses, transcribed text of the responses, as well as "word clouds" generated from the text.
Word clouds are a method of displaying the content of text such that words that are used more frequently are displayed in a larger size than words used less frequently.
Clients will call in to the system approximately twice a week for a period of four months.
Study Type
Interventional
Enrollment (Anticipated)
160
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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California
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Long Beach, California, United States, 90706
- ROADS (Recovery, Opportunity, And Developing Skills)
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Enrolled in the ROADS program
- English speaking
- Have a working telephone
Exclusion Criteria:
- Must speak english
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: HEALTH_SERVICES_RESEARCH
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: My Coach Connect
To evaluate the feasibility and effectiveness of this telephone tool while engaging clients and providers in discussion groups and surveys to better understand how this tool impacts the care provided and their overall experience in healthcare.
Clients will use this tool to leave voice messages and survey answers which their providers will have access to by logging in to a secure website.
Providers will have access to audio recordings of the voice responses, transcribed text of the responses, as well as "word clouds" generated from the text.
Word clouds are a method of displaying the content of text such that words that are used more frequently are displayed in a larger size than words used less frequently.
|
Clients will call in to the system approximately twice a week for a period of four months.
The study will be conducted in two phases.
There will be an initial pilot phase where we will seek to enroll approximately 15-20 patients and 2-3 providers.
This phase will last approximately two months and the goal will be to assess feasibility and obtain feedback on the tool and surveys to optimize them for this setting.
We will begin the main phase of the study approximately one month after the end of the first phase and in that study seek to recruit approximately 150 patients and 5-10 providers from the ROADS program.
Clients enrolled in this main phase of the study will enroll for a period of four months.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Client and provider telephone intervention
Time Frame: four months
|
Clients will call in to an automated telephone system twice a week and will answer open-ended questions related to how they are doing.
In addition, the system will prompt them to complete an automated SF-12 survey every four weeks to assess their mental and physical health status.
The content of the voice messages will be made available to the providers as described above.
Providers will also be able to indicate using the website whether they found a particular narrative helpful or not.
One of the goals of the study is to determine if there is a correlation between the content of the client's messages and their overall health status.
To investigate this, we will combine the content of the voice messages with information obtained from the client's medical record including provider observations, assessment, and symptom recording.
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four months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Client and provider survey
Time Frame: 4 months
|
Each client and provider will be asked to complete a brief survey about their expectations, thoughts and experiences while participating in this study.
The survey will be conducted at the time of enrollment as well as the time of disenrollment or completion of the study as a comparison.
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4 months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Discussion groups
Time Frame: 4 months
|
To better understand the impact of the tool on participants that use it and how to improve the tool, we will also organize discussion groups that clients and providers will have the opportunity to participate in.
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4 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ken Wells, MD, MPH, RAND
- Principal Investigator: Armen Arevian, MD, PhD, University of California, Los Angeles
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2012
Primary Completion (ANTICIPATED)
June 1, 2017
Study Completion (ANTICIPATED)
June 1, 2017
Study Registration Dates
First Submitted
December 11, 2012
First Submitted That Met QC Criteria
December 11, 2012
First Posted (ESTIMATE)
December 13, 2012
Study Record Updates
Last Update Posted (ACTUAL)
May 18, 2017
Last Update Submitted That Met QC Criteria
May 16, 2017
Last Verified
May 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RHINO 2008-0132
- P30MH082760 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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