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NCT06864715Recruiting

Behavioral Activation for the PreVention of Post-strokE Depression in LoW-incomE Older Stroke Survivors

Behavioral Activation for the PreVention of Post-strokE Depression in LoW-incomE Older Stroke Survivors (LIVE-WEL)

Source: ClinicalTrials.gov · Last updated 28 Apr 2026

Brief summary (registry, in English)

The overall objective of the project is to determine the effectiveness of tele-delivered behavioral activation (BA) by trained lay counselors (Tele-BA-S) to prevent Post-stroke depression (PSD) in low-income, older stroke survivors with subthreshold depression (SD).

Status (registry)
Recruiting
Study type
Interventional
Enrollment
350 (estimated)
First submitted
3 Mar 2025
Start date
10 Apr 2026
Primary completion date
1 Nov 2029
Lead sponsor
The University of Texas Health Science Center, Houston
Diseases
Stroke
NCT number
NCT06864715

What you commit to

  • Study type: Interventional
  • Planned participants: 350
  • From 10 Apr 2026 to the primary completion date, 1 Nov 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Diagnosed dementia and/or currently taking cognitive enhancers, amyloid-targeting medications, or orexin receptor antagonists
  • high-risk alcohol or drug misuse
  • receiving medications for mood disorders and a change in dose or type within the last 4 weeks

Other illness

  • Stroke event unrelated to vascular risk factors (e.g., drug use) or transient ischemic attack
  • high suicide risk or severe psychiatric illness (e.g., bipolar disorder and active psychosis) and/or actively taking antipsychotics

Other

  • 24-item HDRS score \> or equal to 15 indicating moderate to severe depression
  • Actively participating in psychotherapy
  • Patient Health Questionnaire 9 score \> or equal to 10 and/or answers positive to Q9
  • Diagnosed aphasia and/or severe cognitive impairments

Who the study is looking for

  • Enrollment within 3-months +2 weeks of a first-time ischemic or hemorrhagic stroke
  • 24-item HDRS score \< 15 indicating subthreshold depression defined as the absence of depressive symptoms or presence of mild symptoms of depression
  • Single person income less than or equal to $45,000
  • Residing in a community residence
  • Ability to speak and read in English or Spanish
  • Mini-MoCA score \> or equal to 11

Age in the registry: 55 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
The University of Texas Health Science Center at Houston
Coordinator of this site? Confirm its status
HoustonUnited StatesRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.