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Empower@Home: A Feasibility Pilot

Empower@Home: A Feasibility Study of a Novel Internet-based Cognitive Behavioral Therapy Program for Depression Among Homebound Older Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05243264
Enrollment
10
Registered
2022-02-17
Start date
2022-02-28
Completion date
2022-08-30
Last updated
2022-09-09

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

Conditions

Depression

Keywords

Cognitive Behavioral Therapy, Older Adults, Internet-Based Intervention, Depression, Social Isolation

Brief summary

This is an open pilot feasibility study of a novel internet-based cognitive behavioral therapy program for older adults with elevated depressive symptoms. This study will enroll approximately 15 older adults throughout the state of Michigan to better understand the feasibility of the intervention and to probe preliminary effects. The intervention will take approximately 10 weeks to complete. Participants will have lower levels of depression after completing the intervention than before enrollment. Participants will be able to use the internet-based platform with minimal support.

Detailed description

Depression affects up to 40% of homebound seniors. The purpose of this research project is to assess the feasibility, acceptability, and preliminary effects of a novel internet-based cognitive behavioral therapy (iCBT) program called Empower@Home. Our team developed Empower@Home collaboratively with older adult stakeholders and social service providers. It is the first iCBT program tailored for low-income racially diverse homebound seniors. It has the potential to reduce access barriers to mental health services among this high-need population. Although Empower@Home is based on an evidence-based mental health treatment (i.e., CBT), it is a novel intervention and has not yet been tested with human subjects. This is a pilot study that involves testing the feasibility, acceptability, and preliminary effects of the intervention with a single group of participants in an open trial. No randomization will occur. All eligible participants who consent will receive the intervention. A total of15 older adults will be recruited to participate in this study. All of them will be recruited through referrals from 2 to 3 social service agencies on this list (The Information Center, Region 2 Area Agency on Aging (AAA), Senior Resources, and A & D home care). The intervention involves attending up to 10 pre-recorded online therapy sessions and receiving weekly maintenance calls from trained research assistants for up to 12 weeks. Participants will engage in therapy at their private homes. A comprehensive baseline and post-test will be administered either over the phone or via an online survey, depending on the participants' preference. No in-person interaction between the participants and the research team is anticipated during the active treatment phase unless intervention is warranted for subjects' safety. Quantitative and qualitative data will be collected and analyzed.

Interventions

BEHAVIORALEmpower@Home

The intervention is a 10-week course of internet-based cognitive behavioral therapy. During the active intervention phase, participants will receive a weekly check-in call to see how they are doing. The weekly check-in call is intended to be brief and last no more than 10 minutes on average.

Sponsors

University of Michigan
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

The purpose of this research project is to assess the feasibility, acceptability, and preliminary effects of a novel internet-based cognitive behavioral therapy (iCBT) program called Empower@Home. The program is intended to decrease depression in participants by encouraging them to participate in meaningful and enjoyable activities while challenging problematic thinking patterns.

Eligibility

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

Inclusion criteria

1. ≥60 years 2. have at least mild depressive symptoms, based on PHQ-9 \>=5 3. are willing to participate

Exclusion criteria

1. Currently receiving CBT or iCBT 2. Probable cognitive impairment based on the Blessed Orientation, Memory, and Concentration scale (score \>= 10). 3. They do not speak English 4. have active suicidal ideation (any positive response on the 9th item of PHQ-9) 5. Have a terminal illness or unstable physical health with a high risk of hospitalization within the next 3 months 6. Severe hearing or vision problems that prevent them from using a tablet/computer or viewing online content

Design outcomes

Primary

MeasureTime frameDescription
Change in Patient Health Questionnaire-9 (PHQ-9)Change from Baseline PHQ-9 at 12 weeksChange in 9 item standardized measures of depressive symptom severity
Modified Treatment Evaluation Inventory12 weeks11-item Likert scale relating to acceptability of program to participant modified for older adults and the study context

Secondary

MeasureTime frameDescription
Change in Generalized Anxiety Disorder Assessment-7 (GAD-7)Change from Baseline at 12 weeksChange in 7-item standardized measure for severity of anxiety symptoms
Change in Duke Social Support Index (DSSI)-10Change from Baseline at 12 weeksChange in 10 item standardized measure for social interaction and satisfaction with social support
Change in PROMISE-SIChange from Baseline at 12 weeksChange in 8 item standardized measure for feelings of loneliness

Countries

United States

Outcome results

None listed

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