Mindfulness training for family caregivers of people with neurodegenerative diseases
Caring for the Family Caregiver: Testing the Effect of Two Wellness Programs That Support the Well-being of Family Caregivers of Persons With Neurodegenerative Disorders
This study is testing if an 8-week mindfulness program can help family caregivers of people with dementia feel less stressed and improve their mental health.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 232 (estimated) |
| Ages | 50 Years to 100 Years |
| Sex | All |
| Sponsor | Toronto Metropolitan University Academic / other |
| Locations | 1 site (Toronto, Ontario) |
| Trial ID | NCT06200909 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of an 8-week mindfulness program aimed at improving the psychological well-being, biological stress indicators, and cognitive function of primary family caregivers for individuals with dementia or related neurodegenerative disorders. Participants, aged 50 and older, will be randomized into three groups: mindfulness meditation, psychoeducation, or a waitlist control. The study will involve three testing sessions to assess changes in stress levels, depressive symptoms, and attentional abilities. All sessions will be conducted virtually via Zoom, with blood samples collected for biological assessments.
Who should consider this trial
Good fit: Ideal candidates are primary family caregivers aged 50 and older who are fluent in English.
Not a fit: Patients who have an existing mindfulness practice or those diagnosed with PTSD, substance disorders, or psychosis may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly enhance the mental and emotional well-being of family caregivers, reducing stress and improving their quality of life.
How similar studies have performed: Previous studies have shown that mindfulness interventions can be beneficial for caregivers, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 50+ years of age * Currently a primary family caregiver * Fluent in English Exclusion Criteria: * Existing mindfulness practice * Diagnosed/Presenting with Post-traumatic Stress Disorder; Substance Disorder; Psychosis * Unable to attend 8 sessions * No access to a computer or high-speed internet * Not willing to be randomized
Where this trial is running
Toronto, Ontario
- Toronto Metropolitan University — Toronto, Ontario, Canada (Recruiting)
Study contacts
- Principal investigator: Alexandra Fiocco, PhD — Toronto Metropolitan University
- Study coordinator: Rhiannon Ueberholz, BA
- Email: star.lab@torontomu.ca
- Phone: 416-979-5000
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.