Reducing mental health issues in caregivers of dementia patients
Reducing Pre-Death Grief, Burden, and Stress in Informal Caregivers: A Group and Individual Therapy Approach
NA · Texas Tech University · NCT05334992
This study is testing different therapy options to see if they can help caregivers of dementia patients feel less stressed and overwhelmed.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 120 Years |
| Sex | All |
| Sponsor | Texas Tech University (other) |
| Locations | 1 site (Lubbock, Texas) |
| Trial ID | NCT05334992 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are informal caregivers, such as spouses, children, or close friends, of individuals diagnosed with dementia.
Not a fit: Patients who are formal caregivers or those with cognitive impairments will not benefit from this study.
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 performed: Other studies have shown success with similar therapeutic approaches for caregiver support, indicating a promising avenue for intervention.
Eligibility criteria
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 this trial is running
Lubbock, Texas
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Mental Health Issue, Grief, Burden, Caregiver