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N/A Completed N=8 Treatment

The Feasibility of Engage Therapy With Video Support for Homebound Older Adults

Source: ClinicalTrials.gov NCT05346055 ↗
Enrolled (actual)
8
Serious AEs
0.0%
Results posted
Jun 2023
Primary outcomePrimary: Acceptability: Client Satisfaction Questionnaire (CSQ) — 10.5 score on a scale

Summary

The primary aim in this pilot project is to test the feasibility, acceptability and impact (decreased depressive symptoms) of a brief behavioral treatment for depression (Engage) combined with video social support (PRISM 2.0) among socially isolated/lonely case management clients who endorse depressive symptoms. Eligible participants will be offered the combination of Engage and Prism 2.0, called Engage-Prism. The investigators hypothesize that the intervention (Engage Therapy With Video Support) will be accepted by participants, improve depressive symptom, and be feasible to complete.

Outcome Measures

OutcomeResultp-value
PRIMARY
Acceptability: Client Satisfaction Questionnaire (CSQ)
9
PRIMARY
Feasibility: Client Enrollment
8
SECONDARY
Hamilton Depression Rating Scale
0.5

Eligibility Criteria

Inclusion Criteria

  • Age at least 60 years
  • 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

  • Psychotic depression by SCID-V, i.e. presence of delusions
  • 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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05346055). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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