- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03555435
Pilot Study of Peer-Supported Online Problem-Solving Program (PS-OPS)
Pilot Study of Standalone and Peer Supported Online Problem Solving Program in Veterans With Untreated Mental Health Problems
Study Overview
Status
Intervention / Treatment
Detailed Description
Approval will be obtained from VA primary care staff leaders at Palo Alto Division and VA Palo Alto Community Based Outpatient Clinics (CBOCs) to mail notes and a study information card to patients who do not have stop codes for mental health or integrated care in their EMR records for the past six months. The study information cards will describe the study, how to enroll, and will direct the Veteran to REDCap eligibility screening questions. When eligibility is confirmed, REDCap will automatically alert research assistant to enroll participant and randomize.
Primary Care Mental Health Integration staff at each clinic may also refer patients to the study by entering referral information directly into secure, encrypted REDCap files or by handing the patient a study information card.
Community veterans will be invited via social media marketing. Ads will link to a study web site. Study web site will link potential participants to REDCap eligibility screening questions. When eligibility is confirmed, REDCap will automatically alert research assistant to enroll participant and randomize.
Veterans who decide to be in the study will be assigned by chance to one of three groups: An On Your Own group, a Peer Support group, or a Wait group. Veterans assigned to take the Moving Forward course with peer support or on their own will complete the course online and practice the problem-solving skills they learned for six weeks. Finishing the Moving Forward course takes a total of about four hours. Veterans in the peer support group will speak with a Veteran who is experienced with the course on the phone for 15 to 20 minutes once a week during the study about using the ideas and exercises in the course to solve problems. Veterans assigned to the wait group will answer questions online about problem-solving skills and their well-being at the start and after six weeks). They will be able to take the course if they would like to after the six weeks have passed. Veterans in the On Your Own and Peer Support groups will answer questions online at the beginning, middle, and end of the study about problem-solving skills, their opinions about the course and about peer support (if they got it), and their well-being. This will take 10 to 15 minutes each time.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
California
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Palo Alto, California, United States, 94304-1207
- VA Palo Alto Health Care System, Palo Alto, CA
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- A Veteran of one of the U.S. military services, including National Guard and Reserves.
- Positive screen (score of 1 or more) on the PHQ-2 or GAD-2.
- Access to a phone and to a desktop or laptop computer with internet access.
- Willingness to be randomized to one of three conditions.
- Willingness to work with a Peer Support Specialist.
Exclusion Criteria:
- An active suicide plan.
- Changes in psychoactive medications in the past month.
- MH treatment in the past 6 months, including treatment from a PC-MHI team member.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: On Your Own
Participants in this group will use the online program on their own for 6 weeks.
|
Participants in this group will use the online program on their own for 6 weeks.
|
Experimental: Peer Support
Participants in this group will use the online program on their own for 6 weeks with the support of a peer coach.
Peer coaching sessions will consist of 6 15-20 minute sessions one time per week.
Sessions will be guided by a Moving Forward Peer Support Manual.
|
Participants in this group will use the online program on their own for 6 weeks with the support of a peer coach.
Peer coaching sessions will consist of 6 15-20 minute sessions one time per week.
Sessions will be guided by a Moving Forward Peer Support Manual.
|
Placebo Comparator: Wait
Participants in this group will wait 6 weeks.
|
Participants in this group will wait 6 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Problem-Solving Skills, Knowledge, and Abilities Test
Time Frame: change from baseline to study end (6 weeks)
|
The Problem-Solving Skills, Knowledge, & Abilities Test is a brief, multiple-choice test that measures mastery of the basic concepts and skills that are included in the Moving Forward program.
Scores on the test can range from 0 to 12 with higher scores indicating greater problem-solving skills, knowledge, and abilities.
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change from baseline to study end (6 weeks)
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Problem-Solving Confidence
Time Frame: change from baseline to study end (6 weeks)
|
The Problem-Solving Confidence Test assesses participant's confidence in his/her own problem solving abilities.
Scores on this measure can range from 0 to 9 with higher scores indicating greater problem-solving confidence.
|
change from baseline to study end (6 weeks)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
GAD-7 Change
Time Frame: change from baseline to study end (6 weeks)
|
The GAD-7 assesses the severity of anxiety symptoms associated with generalized anxiety in terms of the proportion of days assessed in which the symptoms were present.
Score range 0-21.
Positive values for change from baseline to study end represent decreases in anxiety.
Negative values for change from baseline to end represent increases in anxiety.
|
change from baseline to study end (6 weeks)
|
Posttraumatic Stress Symptoms Change
Time Frame: change from baseline to study end (6 weeks)
|
Symptom change was measured by 7 items from the Screen for Posttraumatic Stress Symptoms (SPTSS) and 4 items from the Dissociative Symptoms Scale (DSS).
Scores for all items could range from 0 to 47. Scores on change could range from -47 to 47. Positive values for change from baseline to study end represent reductions in PTSD symptoms.
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change from baseline to study end (6 weeks)
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WHO-5 Well-Being Index Change
Time Frame: change from baseline to study end (6 weeks)
|
The World Health Organization Well-Being Index (WHO-5) is a widely-used 5-item measure assessing subjective psychological well-being.
Its design for use around the world and translation into 30 languages are indicative of its usefulness as a measure for a diverse population.
Score range 0-25.
Positive changes from baseline to study end represent decreases in well-being.
Negative values for change from baseline to end represent increases in well-being.
|
change from baseline to study end (6 weeks)
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PHQ-9 Change
Time Frame: change from baseline to study end (6 weeks)
|
The PHQ-9 assesses the severity of depression in terms of the proportion of days assessed in which the symptoms were present.
Score range 0-27.
Positive values for change from baseline to end represent reductions in depression.
Negative values for change from baseline to end represent increases in depression.
|
change from baseline to study end (6 weeks)
|
Client Satisfaction Questionnaire
Time Frame: at study end (6 weeks)
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The Client Satisfaction Questionnaire (CSQ) is a standardized, widely-used measure of customer satisfaction with health services and programs.
Total scores on the 7-items we used range from 7 to 28.
Higher scores represent greater satisfaction.
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at study end (6 weeks)
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Stigma Measure (EZ-EASI)
Time Frame: measured once at baseline
|
The Endorsed and Anticipated Stigma Inventory (EASI) is a tool for assessing different dimensions of stigma-related beliefs about mental health among military and veteran populations.
Findings based on a national sample of U.S. veterans deployed in support of Operation Enduring Freedom (OEF) in Afghanistan or Operation Iraqi Freedom (OIF) in Iraq suggest that the EASI is a psychometrically sound instrument.
Specifically, results revealed evidence for the internal consistency reliability, content validity, convergent and discriminant validity, and discriminative validity of EASI scales.
Total scores on 13 items used range from 0 to 39. Higher scores represent greater endorsement of stigma-related beliefs.
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measured once at baseline
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Moving Forward Usage
Time Frame: daily for 6 weeks
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Usage was assessed by total number of days logging in to online course Moving Forward.
This data was collected daily and automatically during study participation.
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daily for 6 weeks
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Collaborators and Investigators
Investigators
- Principal Investigator: Eve Bernstein Carlson, PhD, VA Palo Alto Health Care System, Palo Alto, CA
Publications and helpful links
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
- PPO 16-323
- HX-002361-01 (Other Grant/Funding Number: VA Health Services R & D)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
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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