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NCT05465109Completed

Traumatic Brain Injury and Alzheimer's Disease/Related Dementias Caregiver Support Intervention

Designing and Evaluating a Comprehensive Support Program for Families Caring for Relatives Living With TBI-AD/ADRD

Source: ClinicalTrials.gov · Last updated 22 Dec 2025

Brief summary (registry, in English)

The TBI-AD/ADRD Caregiver Support Intervention (TACSI) incorporates psychosocial and psychoeducational approaches with the objective of: a) identifying stressors associated with caregiving for family members who have the dual diagnosis of traumatic brain injury and dementia; and b) supporting caregivers in developing more effective coping and communication strategies as well as enhanced caregiving self-efficacy.

Status (registry)
Completed
Study type
Interventional
Enrollment
95 (actual)
First submitted
15 Jul 2022
Start date
1 Jul 2022
Primary completion date
28 Jun 2025
Lead sponsor
University of Minnesota
NCT number
NCT05465109

What you commit to

  • Study type: Interventional
  • Participants enrolled: 95
  • From 1 Jul 2022 to the primary completion date, 28 Jun 2025
  • 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

  • caregivers who have a new or worsening mental health condition and are not receiving ongoing treatment. When applicable, if caregivers have not remained on a stable psychotropic medications dosage, such as antidepressants, anxiolytics or anti-psychotics, for the prior three months they will be excluded.

Who the study is looking for

  • the care recipient has a physician diagnosis of TBI and AD/ADRD (i.e., those with a diagnosis of both TBI and progressive cognitive decline)
  • the caregiver self-identifies as someone who provides the most help/is most responsible for the person with TBI-AD/ADRD because of their cognitive impairments (or shares the role equally with another caregiver)
  • the caregiver indicates a willingness to participate in the TACSI evaluation
  • the caregiver is English speaking
  • the caregiver is 21 years of age or older
  • the caregiver is not currently participating in any other type of service that provides one-to-one psychosocial consultation or caregiver coaching (peer mentorship/support group participation/general counseling not specific to caregiving is not a deterrent to enrollment) at the discretion of the UMN research team
  • the caregiver resides in the US.

Age in the registry: 21 years to - · Sex: All · Accepts 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
University of Minnesota
Coordinator of this site? Confirm its status
MinneapolisUnited StatesUnknown status

Related publications

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