- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03151083
Implementing and Evaluating Computer-Based Interventions for Mental Health: Testing an Implementation Strategy for VA Outpatient Care
Implementing and Evaluating Computer-Based Interventions for Mental Health (CDA 14-420)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Objective: The purpose this study is to evaluate the preliminary (1) effectiveness of an implementation strategy for Internet-based Self-help Interventions and (2) clinical outcomes of a specific Internet-based self-help program for insomnia, SHUTiTM, in VA Connecticut outpatient primary care. The primary hypothesis is that the experimental implementation strategy the investigators are developing, relative to a control strategy, will result in higher rates of program engagement by patients, greater provider adoption through referral to the program, greater program completion, and improved patient insomnia outcomes.
Research Design: The investigators will employ a hybrid implementation-effectiveness study design through which the investigators will primarily test the effectiveness of the implementation strategy, while secondarily evaluating the clinical effectiveness of the SHUTiTM program. The investigators will use a quasi-experimental pre-/post-cohort design whereby SHUTiTM will initially be implemented using a low-intensity (control) strategy, followed by implementation using the experimental strategy. The SHUTiTM program's association with clinical response will be evaluated in an uncontrolled pre-/post-format.
Methodology: Internet-based self-help programs are personalized, self-guided interventions delivered over a computer, mobile device, or other Internet platform and focused on improving knowledge, awareness, or behavior change for a mental or physical health problem. Through previous and on-going projects at VACT, the investigators are developing a general strategy for implementing Internet-based Self-help programs in VA primary care, specifically among Patient Aligned Care Teams (PACT) and Primary Care Mental Health Integration (PCMHI) providers. An implementation strategy is defined as a systematic intervention to integrate evidence-based health innovations into usual care. The strategy the investigators propose to test consists of four core components: (1) a clinical intermediary for patient support, (2) provider/staff facilitation and education, (3) patient education, and (4) stepped-care for those requiring additional treatment. The investigators' currently approved protocol (#0002) involves interviewing VA providers, administrators, and staff in order to expand and modify the components of this strategy. In the proposed study, the investigators will compare this strategy to a low intensity (control) strategy with respect to the implementation related outcomes of patent engagement, provider adoption through referral to the program, and patient completion, over a six-month active implementation period. Use of the program will continue and implementation outcomes will be gathered over an additional one-year sustainment phase. The investigators will target the very common clinical problem of insomnia and use the SHUTiTM program, a 6-week self-guided program utilizing standard cognitive-behavioral therapy (CBT) techniques for the treatment of chronic insomnia. The program has been shown to improve insomnia severity and other sleep related outcomes in a number of controlled trials. The clinical effectiveness of SHUTiTM will be evaluated using clinical insomnia outcomes obtained on all patients enrolled over the 6-month active implementation periods.
Impact/Significance: The development and testing of evidence-based implementation strategies for Internet-based self-help programs in VA outpatient care is essential given that (1) there is an increasing number of Internet-based self-help programs providing evidence-based treatment for a variety of mental and behavioral health disorders, (2) VA has committed to improving access to care, especially evidence-based and self-care resources, and (3) there is a Congressional mandate that VA implement Internet-based care. This will be first controlled trial of an implementation strategy for Internet-based self-help programs in a VA primary care (PACT/PCMHI) context.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Connecticut
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West Haven, Connecticut, United States, 06516-2770
- VA Connecticut Healthcare System West Haven Campus, West Haven, CT
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients Receiving care from a VA Connecticut West Haven PACT/PCMHI Provider
- Diagnosed with insomnia lasting 3 months by the PACT provider, as evidenced by referral by the provider for access to the SHUTiTM program
- Able to provide valid informed consent, as evidenced by answering questions indicating their understanding of the content of the Informed Consent Document
- Willing to participate in an internet-based self-help program for insomnia after the access to and requirements of the program are explained to them
- English-speaking (The SHUTiTM program is only available in English)
Exclusion Criteria:
- Evidence of acute psychiatric decompensation requiring inpatient admission or emergency department services within the last month, including suicidality, homicidally, mania, or psychotic decompensation.
- Evidence of a conservator of person either verbally reported by the patient or upon inspection of the medical record.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Phase 1: Implementation As Usual (Implementation Through Rese
SHUTi digital CBTi Program was implemented in VACT primary care using implementation activities executed by the research team between June 2017 and January 2018 (8-months).
Implementation activities included: Provider Education by the research team, Provider Reminders (information pamphlets in treatment rooms), Patient Advertising/Information (information pamphlets in treatment rooms), Single Referral Pathway Not Integrated Primary Care Workflow (Primary care provider contact research team for patient referral over email).
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The investigators will use the program, SHUTiTM for the treatment of insomnia.
The intervention is a CBT-based 6-week, self-administered course accessed via the Internet on mobile, desk-top, and other devices.
The program is split into six modules, completed weekly, which include instruction on psycho-education, stimulus control, relaxation training, sleep restriction, medication tapering, and addressing cognitive distortions.
The content is delivered via text, video vignettes, case histories, interactive learning tools, interactive skills assessments, symptom assessments, and a sleep log.
Homework is assigned after each module.
Providers and support staff can follow treatment progress via access to a dashboard of patient information collected by the program.
Such information includes progress through the modules, date of last engagement, symptom assessment outcomes, and sleep log data abstracted into commonly used sleep indices such as sleep onset latency and sleep efficiency.
Other Names:
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Experimental: Phase 2: Primary Care Coached Digital CBTi Implementation (Im
SHUTi digital CBTi Program implemented in VACT primary care using implementation activities executed by primary care teams June 2018 and January 2019 (8-months).
Implementation activities included: Provider Education by the research team, Provider Reminders (information pamphlets in treatment rooms), Patient Advertising/Information (information pamphlets in treatment rooms), patient education and motivational support supplied through a digital CBTi coach, the digital CBTi coach was a primary care nurse trained by the research team, technical support and oversight of the digital CBTi coach by the research team.
Single Referral Pathway Not Integrated Primary Care Workflow.
|
The investigators will use the program, SHUTiTM for the treatment of insomnia.
The intervention is a CBT-based 6-week, self-administered course accessed via the Internet on mobile, desk-top, and other devices.
The program is split into six modules, completed weekly, which include instruction on psycho-education, stimulus control, relaxation training, sleep restriction, medication tapering, and addressing cognitive distortions.
The content is delivered via text, video vignettes, case histories, interactive learning tools, interactive skills assessments, symptom assessments, and a sleep log.
Homework is assigned after each module.
Providers and support staff can follow treatment progress via access to a dashboard of patient information collected by the program.
Such information includes progress through the modules, date of last engagement, symptom assessment outcomes, and sleep log data abstracted into commonly used sleep indices such as sleep onset latency and sleep efficiency.
Other Names:
|
Experimental: Phase 3: Primary Care Mental Health Collaborative Care Implem
SHUTi digital CBTi Program implemented in VACT primary care using implementation activities executed by primary care teams April 2019 and November 2019 (8-months).
Implementation activities included: Provider Education by the research team, Provider Reminders, Patient Advertising/Information, patient education and motivational support supplied through a digital CBTi coach, the digital CBTi coach was a peer support specialist working on the primary care mental health collaborative care team, the digital CBTi coach was trained by the research team, technical support and oversight of the digital CBTi coach by the research team.
Additional members primary care mental health collaborative care team were educated to provide education about digital CBTi.
Multiple referral pathways to digital CBTi: consults to the digital CBTi Coach, warm handoffs to primary care mental health collaborative care team.
Digital CBTi coach consults integrated Primary Care Workflow.
|
The investigators will use the program, SHUTiTM for the treatment of insomnia.
The intervention is a CBT-based 6-week, self-administered course accessed via the Internet on mobile, desk-top, and other devices.
The program is split into six modules, completed weekly, which include instruction on psycho-education, stimulus control, relaxation training, sleep restriction, medication tapering, and addressing cognitive distortions.
The content is delivered via text, video vignettes, case histories, interactive learning tools, interactive skills assessments, symptom assessments, and a sleep log.
Homework is assigned after each module.
Providers and support staff can follow treatment progress via access to a dashboard of patient information collected by the program.
Such information includes progress through the modules, date of last engagement, symptom assessment outcomes, and sleep log data abstracted into commonly used sleep indices such as sleep onset latency and sleep efficiency.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Program Engagement: Completion of the First Program Module
Time Frame: 3 weeks following subject enrollment
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The proportion of participants engaging in the program (completing at least one module) among the unique Veterans treated in VA Connecticut primary care over the respective intervention periods.
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3 weeks following subject enrollment
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Program Completion
Time Frame: 10 Weeks following subject enrollment
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Completion of all six modules of the program.
The proportion of individuals completing all six modules among all individuals enrolled.
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10 Weeks following subject enrollment
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Provider Adoption
Time Frame: Over each 8-month active implementation Phase
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The number of providers who made a referral to the SHUTi Program among the number of providers with the ability to make a referral.
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Over each 8-month active implementation Phase
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Insomnia Severity Index
Time Frame: At enrollment and 10 weeks following enrollment.
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The ISI will be the primary clinical outcome and is a self-report seven-item measure that targets the subjective symptoms and functional consequences of insomnia.
The outcome reported is the change in total ISI score from baseline to follow-up.
All enrollees are analyzed as a single group regardless of implementation period.
The Insomnia Severity Index to total is the sum on 7 questions scored 0 to 4 (minimum=0, Maximum=28).
Higher scores indicate more severe insomnia.
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At enrollment and 10 weeks following enrollment.
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Beck Depression Inventory
Time Frame: At enrollment and 10 weeks following enrollment
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The BDI is a secondary clinical outcome and is a self-report measure of depression severity.
The outcome reported is the change in total BDI score from baseline to follow-up.
All enrollees are analyzed as a single group regardless of implementation period.
The BDI is a 21-item, self-report rating inventory of depression symptoms.
Items receive a rating of zero to three and are summed linearly to create a score which ranges from 0 to 63.
Higher score indicate more intense symptoms of depression.
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At enrollment and 10 weeks following enrollment
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Sedative-Hypnotic Medication Use
Time Frame: At enrollment and 10 weeks following enrollment
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The use of sedative-hypnotics will be measured by self-report of the type and dose of specific medications used in the last week.
The outcome reported is the change in the reported total weekly number of sedative-hypnotic doses reported from baseline compared to follow-up.
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At enrollment and 10 weeks following enrollment
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Collaborators and Investigators
Investigators
- Principal Investigator: Eric Hermes, MD, VA Connecticut Healthcare System West Haven Campus, West Haven, CT
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- CDX 16-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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