Reducing mental health issues in caregivers of dementia patients
Official title: Reducing Pre-Death Grief, Burden, and Stress in Informal Caregivers: A Group and Individual Therapy Approach
Run by Texas Tech University · NCT05334992 · Data updated 2026-11-12
This study is testing different therapy options to see if they can help caregivers of dementia patients feel less stressed and overwhelmed.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 120 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Texas Tech University Academic / other |
| Locations | 1 site (Lubbock, Texas) |
| Status | Recruiting |
| Started | February 1, 2022 |
| Main results expected | December 31, 2028 |
| Study ends | December 31, 2028 |
| Registry record updated | February 12, 2026 |
| Trial ID | NCT05334992 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are informal caregivers, such as spouses, children, or close friends, of individuals diagnosed with dementia.
✕Probably not a fit
Patients who are formal caregivers or those with cognitive impairments will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This project aims to evaluate the effectiveness of evidence-based interventions in reducing psychological distress, burden, and stress among informal caregivers of individuals with dementia. The study will assess two individual therapies, Mindfulness Based Cognitive Therapy and Behavior Activation, as well as a modified group therapy approach. By focusing on the mental health of caregivers, the study seeks to provide targeted support to those who play a crucial role in the care of dementia patients.
Why it matters
Potential benefit: If successful, this study could significantly improve the mental health and well-being of informal caregivers, enhancing their ability to provide care.
How similar studies have gone: Other studies have shown success with similar therapeutic approaches for caregiver support, indicating a promising avenue for intervention.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participants must be informal caregivers (e.g., spouse; child; close friend) of individuals with dementia * Informal caregivers can be family members or close friends * Adults (18 to 89 years old) who read, write, and speak in English * Mental Health Diagnosis (e.g., Generalized Anxiety Disorder; Major Depressive Disorder Exclusion Criteria: * Formal caregivers (who are being paid to take care of the patient) * Any informal caregivers with cognitive impairment is identified during the assessment.
Where it's running
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Texas Tech University
Lubbock, Texas, United States Recruiting
Study contacts
- Principal investigator: Jonathan D Singer, Ph.D — jonsinge@ttu.edu
- Study coordinator: Casside Street, Ph.D
- Email: casside.street@ttu.edu
- Phone: (806) 834-2285
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.