The Feasibility of Engage Therapy With Video Support for Homebound Older Adults
NCT ID: NCT05346055
Last Updated: 2023-06-28
Study Results
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View full resultsBasic Information
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COMPLETED
NA
8 participants
INTERVENTIONAL
2022-05-12
2022-09-30
Brief Summary
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Detailed Description
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Participants will be referrals from case management service. Clinicians will incorporate elements of the Prism system into therapy as appropriate, and participants will be instructed to use the Prism system at their leisure or as it pertains to their chosen "reward exposure" activities. There will be a post-therapy assessment and interview about their experience with the technology at week 9. The study will conclude with follow-up assessments at week 12.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Engage Prism 2.0
Engage Prism is a 9-week program that integrates Engage- a form of behavioral talk therapy treating depression, and guided use of Prism technology- a software that aims to improve social support and interaction of older adults.
Engage Prism (2.0)
Brief Behavioral Treatment for Depression (Engage) combined with tablet-based social support system (Prism 2.0)
Interventions
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Engage Prism (2.0)
Brief Behavioral Treatment for Depression (Engage) combined with tablet-based social support system (Prism 2.0)
Eligibility Criteria
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Inclusion Criteria
* English speaking
* Currently enrolled in case management at in 2 included agencies
* Major depression on the SCID
* 24-item Hamilton Depression Rating Scale (HAM-D) ≥ 19
Exclusion Criteria
* High suicide risk, i.e. intent or plan to attempt suicide in the near future
* Presence of any Axis I psychiatric disorder
* Presence of substance abuse other than unipolar major depression
* History of psychiatric disorders, hypomania, are excluded
* Acute or severe medical illness, i.e. delirium, metastatic cancer, decompensated cardiac, liver, or kidney failure, major surgery, stroke, or myocardial infarction during the three months prior to entry; or drugs often causing depression, e.g. steroids, reserpine, alpha- methyl-dopa, tamoxiphen, vincristine
* Current involvement in psychotherapy
* Cognitive impairment (i.e. telephone administered MoCA \< 11)
* Currently dwelling in non-community dwelling (e.g. prison, nursing home)
* Hearing that would not allow participants to complete sessions with the RA/therapist
* Vision impairment that would not allow the participant to use the study provided tablet
* Inability to speak English
* Aphasia interfering with communication
* Literacy -assessed by reading a paragraph designed for those at 6th grade reading level
60 Years
ALL
No
Sponsors
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National Institute of Mental Health (NIMH)
NIH
Weill Medical College of Cornell University
OTHER
Responsible Party
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Principal Investigators
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Natalie C Benda, PhD
Role: PRINCIPAL_INVESTIGATOR
Weill Medical College of Cornell University
Locations
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Weill Cornell Medicine
New York, New York, United States
Countries
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Provided Documents
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Document Type: Study Protocol
Document Type: Statistical Analysis Plan
Other Identifiers
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20-10022828
Identifier Type: -
Identifier Source: org_study_id
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