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Management of Depression and Social Isolation in Older Adults With Dementia With Home-based Telehealth Delivered Behavioral Activation + Caregiver Facilitation.

Management of Depression and Social Isolation in Older Adults With Dementia With Home-based Telehealth Delivered Behavioral Activation + Caregiver Facilitation.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04915040
Enrollment
7
Registered
2021-06-07
Start date
2021-07-01
Completion date
2022-07-19
Last updated
2023-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression

Keywords

social support, dementia, caregivers

Brief summary

The purpose of this study is to evaluate the feasibility of using behavioral activation therapy with caregiver support delivered via telemedicine to older adults with depression and probable mild dementia.

Interventions

BEHAVIORALBehavioral Activation for Depression

Behavioral Activation (BA) is an effective treatment for depression, and its components may increase social connection. Generally, caregivers are with the older adult care recipient on a regular basis and may be able, with the correct training, to help enhance certain features of the Behavioral Activation treatment, even under pandemic restrictions on social contact. Therefore, we propose to (a) integrate & (b) gather feasibility data for home-based Behavioral Activation + Caregiver

Sponsors

The University of Texas Health Science Center, Houston
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Participant Eligibility Criteria: * able to speak and understand English; * a diagnosis of mild dementia, as determined by a Clinical Dementia Rating interview Sum of Boxes (CDR-SB) score in the mild range as defined by a score of 4.5 - 9.0; * and able to provide informed consent. Caregiver Eligibility Criteria. * Beck Depression Inventory (BDI) score below clinical cutoff for depression and able to provide informed consent.

Exclusion criteria

Participant

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of recruitment as assessed by number of participants enrolled in the studyWeek 0
Feasibility of retention as assessed by number of participants who complete at least 6 sessionsWeek 8
Feasibility of data collection as assessed by percent of missing dataWeek 8
Change in Depression as measured by the Geriatric Depression ScaleWeek 0, Week 4, Week 815-item self-report for each construct (yes/no) . Score goes from 1 to 15, a higher number indicates presence of depression.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026