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Meditation and Psychophysical Well-Being in Elderly

StatusActive, Not Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

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  1. Minor Enrollment closed, study ongoing
    • Study completion pushed from Nov 1, 2025 to Nov 1, 2026
    • Site details revised
    v3
  2. Minor Study description revisedv2
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this experimental study is to assess whether a mindfulness-based meditation intervention can reduce loneliness and improve psychophysical well-being in older adults (aged 65 and above). The main questions it aims to answer are: * Does the intervention reduce the perception of loneliness in older adults? (primary outcome) * Does it improve various aspects of psychological well-being, including social isolation, depression, life satisfaction, mindfulness, emotional regulation, self-acceptance, and sleep quality? (secondary outcomes) Researchers will compare the intervention group with a passive control group (waiting-list control) to determine whether the mindfulness-based intervention leads to significant improvements in the measured outcomes. Participants will: Complete baseline assessments, including neuropsychological tests and validated questionnaires, before the intervention. Undergo a 12-session mindfulness-based intervention over 6 weeks, consisting of guided breathing, focused attention, physical relaxation, and emotional awareness exercises. Complete post-intervention assessments to measure changes in their psychological and physiological well-being.
Trial Details
NCT Number NCT06872502
Lead Sponsor University of Pavia
Conditions
(from sponsor)
Loneliness, Psychophysical Well-being
Related terms Social Isolation
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov