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Clinical Trials in Canada / NCT06200909
Recruiting Not applicable

Self-Care Training for Family Caregivers of Persons With Neurodegeneration

NCT06200909 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2024-06
Last updated
2024-04-10

Condition(s) studied

Caregiver BurdenCaregiver Stress

Investigational drug(s) / intervention(s)

Mindfulness MeditationPsychoeducationWait list control

Mindfulness Meditation: 8-week mindfulness meditation program, based on Kabat-Zinn's MBSR program and modified for caregivers. The intervention will be led by MBSR-trained facilitators.

Psychoeducation: A lecture-style program based on the "10 Keys"TM to Healthy Aging Course, an evidence-based program for older adults. The program will be delivered by a facilitator experienced in delivering similar content.

Wait list control: Participants will receive two hours of respite from their caregiving responsibilities per week, for eight weeks. They will be given the opportunity to participate in either the MM or the PSY condition following completion of testing.

Study summary

The purpose of this study is to assess whether an 8-week mindfulness program enhances psychological well-being (e.g., stress, depressive symptoms), biological indicators of stress (e.g., inflammation), and cognitive function (e.g., attentional ability) in primary family caregivers of persons with dementia or a related neurodegenerative disease. A total of 232 primary family caregivers aged 50+ years of age will be recruited for this study and randomized to one of three groups: mindfulness meditation (MM), psychoeducation (PSY) or caregiver respite (CR). All participants will complete three testing sessions: baseline (pre-intervention \[T1\]), post 8-week follow-up (post-intervention, \[T2\]), and 12-month follow-up (T3).

Eligibility

Sex
ALL
Min age
50 Years
Max age
100 Years
Healthy volunteers
Accepted
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Toronto Metropolitan University Toronto Ontario Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06200909 on ClinicalTrials.gov ↗ ← All trials in Canada