Actively Recruiting

Phase Not Applicable
Age: 50Years - 100Years
All Genders
NCT05011864

Integrated Tele-Behavioral Activation and Fall Prevention for Low-income Homebound Seniors With Depression

Led by University of Texas at Austin · Updated on 2024-01-09

320

Participants Needed

1

Research Sites

269 weeks

Total Duration

On this page

Sponsors

U

University of Texas at Austin

Lead Sponsor

B

Baylor College of Medicine

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study will test clinical and cost effectiveness of an integrated tele- and bachelor's-level counselor/coach delivered behavioral activation (BA) and fall prevention (FP) for low-income homebound older adults. The long-term objective of the proposed study is to improve access to depression treatment and fall prevention for growing numbers of low-income homebound seniors. We plan to recruit 320 low-income, racially diverse homebound seniors who are served by a home-delivered meal (HDM) program and other aging-service agencies in Central Texas. In a 4-arm, pragmatic clinical trial with randomization prior to consent, the participants in the integrated Tele-BA and FP (TBF hereafter) arm will receive 5 Tele-BA sessions and 4 in-home FP sessions. Those in the Tele-BA or FP alone arms will receive the respective intervention and 4 bimonthly telephone check-in (booster) calls, and those in the Attention Control (AC) arm will receive 5 weekly telephone check-in calls followed by 4 bimonthly follow-up calls. Follow-up assessments will be at 12, 24, and 36 weeks after baseline.

CONDITIONS

Official Title

Integrated Tele-Behavioral Activation and Fall Prevention for Low-income Homebound Seniors With Depression

Who Can Participate

Age: 50Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 50 years or older
  • Able to speak English or Spanish
  • Hamilton Rating Scale for Depression 24-item score greater than 15
  • Fall Risk Questionnaire 12-item score greater than 4
Not Eligible

You will not qualify if you...

  • Started or changed antidepressant medication within the last 4 weeks
  • High risk of suicide
  • Probable dementia diagnosis
  • Diagnosis of bipolar disorder
  • Substance use or misuse
  • Currently participating in any psychotherapy or fall prevention program
  • Bedbound status

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Texas at Austin

Austin, Texas, United States, 78712-0358

Actively Recruiting

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Research Team

N

Namkee G Choi, PhD

CONTACT

K

Kelly Vences, BSW

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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