Skip to main content
Clinical Trials/NCT03854045
NCT03854045
Unknown
Not Applicable

Team-based Telemedicine

Wayne State University1 site in 1 country160 target enrollmentFebruary 1, 2019
ConditionsMental Disorder

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mental Disorder
Sponsor
Wayne State University
Enrollment
160
Locations
1
Primary Endpoint
PHQ-9
Last Updated
7 years ago

Overview

Brief Summary

Telemedicine can expand access to behavioral health services for people who have difficulty traveling to clinics. Travel can be especially challenging for older adults with mobility issues or access to reliable transportation. Assessment in the home can uncover factors impacting patient's physical and behavioral health. The goals of this project to document benefits and barriers to expanding reimbursement for telemedicine to older patient's home as the originating site.

Detailed Description

The goal of this project is to document the benefits and barriers to expanding reimbursement for telemedicine to older patient's home as the originating site. The objectives are: * Develop training module for midlevel clinicians to be ready for dissemination * Improved patient outcomes measures on satisfaction with care; functioning and symptoms (anxiety, depression, traumatic stress, sleep apnea, alcohol use and problems) * Reductions in emergency healthcare utilization and medications prescribed as obtained from electronic health record (EHR) at the Federally Qualified Health Center (FQHC) and self-reports * Summarize activities and barriers, including communication with primary care provider, identification and improvement of home environmental risks, and assistance to support system This is an observational study of team-based telepsychiatry in the home for one group and team-based psychiatry in the clinic for the comparison group. The initial assessment will include information and informed consent for treatment, biopsychosocial assessment, summary for the psychiatrist, psychiatric evaluation and recommendations (all standard of care). To that the investigators are adding informed consent for program evaluation with 6 month follow-up with information for re-contacting (3 sources, addresses, email-telephone numbers), and brief administration of selected instruments before informed consent for treatment. If an eligible patient does not want to participate in the research study, the patient would still receive services. Additional telemedicine sessions and/or therapy sessions will be conducted as medically needed in accordance with quality care. At six months (with one month window on either side) the evaluation packet will be re-administered by the clinician if convenient or by the research assistant either in person or by phone. The sample size was selected to provide robust indicators of barriers to home based assessments. The comparison group was included to provide a context for the findings. It is anticipated that the home group will have greater problems at baseline than the clinic based comparison group but both will show improvements.

Registry
clinicaltrials.gov
Start Date
February 1, 2019
End Date
December 2020
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Cynthia L. Arfken, PhD

Professor

Wayne State University

Eligibility Criteria

Inclusion Criteria

  • patient at FQHC
  • referred for psychiatric services
  • 50 or older

Exclusion Criteria

  • does not speak English

Outcomes

Primary Outcomes

PHQ-9

Time Frame: 6 months

depressiive symptoms

Secondary Outcomes

  • GAD7(6 months)
  • Home checklist(6 months)

Study Sites (1)

Loading locations...

Similar Trials