Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
60 participants
INTERVENTIONAL
2025-02-15
2025-11-01
Brief Summary
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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.
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Detailed Description
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Unfortunately, at least nine million elderly individuals in Italy live alone or are at risk of social isolation. According to data from the "Passi d'Argento" surveillance system of the Italian National Institute of Health (Istituto Superiore di Sanità), this phenomenon affects 1 in 7 people over 65. Social isolation significantly impacts healthy aging, compromising both physical and mental well-being.
Social isolation consists of two components: an objective one and a subjective one, namely loneliness. These two dimensions do not always correlate and affect health through different pathways: the former is more closely linked to physical health, while the latter is primarily associated with mental health.
Several risk factors contribute to this condition (e.g., educational level, environment in which a person was raised, comorbidities, income, etc.), also influencing coping mechanisms. Addressing this social and economic challenge requires timely and sustainable interventions. In this context, mindfulness represents a promising therapeutic and preventive tool.
Mindfulness-based interventions are easily accessible, simple to implement, and have a low economic impact, while promoting both physical and mental health. They foster psychological well-being and personal growth, encouraging a non-judgmental awareness of the present moment. Mindfulness can help older adults accept the changes and losses associated with aging, enhancing self-awareness and developing new coping strategies. Furthermore, mindfulness may serve as a tool to recognize and understand loneliness, potentially transforming it into an opportunity for personal growth.
By promoting active listening, empathy, and self-esteem, mindfulness can also contribute to improving the quality of social relationships. However, studies exploring the effects of mindfulness on loneliness-particularly in older adults-are still limited and often involve small sample sizes and lack comprehensive sociodemographic data.
The objective of this study is to evaluate the impact of a mindfulness-based meditation intervention on the sense of loneliness (primary outcome) as well as on various domains of psychophysical well-being in older adults.
Specifically, the following hypotheses will be tested:
i) The intervention reduces the sense of loneliness (primary outcome); ii) It decreases objective social isolation; iii) It lowers depression levels, contributing to an overall improvement in psychological well-being; iv) It enhances mental well-being and life satisfaction; v) It improves mindfulness and promotes emotional regulation; vi) It fosters greater self-acceptance in terms of body appreciation and enhances self-esteem; vii) It improves sleep quality.
The target population will consist of older adults aged 65 and above, recruited on a voluntary basis.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
Participants are randomized into these two groups and followed in parallel without switching between conditions.
The outcomes are measured before and after the intervention, comparing the effects between the two groups.
TREATMENT
DOUBLE
Study Groups
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Mindfulness-Based Intervention Group
Participants in this group will undergo a mindfulness-based meditation intervention called Integral Meditation (IM). The intervention consists of 12 in-person sessions over six weeks, with each session lasting one hour, twice per week. The meditation techniques will include focused breathing, body relaxation, emotional awareness, and acceptance exercises.
Mindfulness-Based Meditation (Integral Meditation - IM)
The intervention consists of 12 in-person mindfulness-based meditation sessions over a period of six weeks, with each session lasting one hour, twice per week. The practice, called Integral Meditation (IM), includes focused breathing, body relaxation, emotional awareness, and acceptance exercises.
Waiting-List Control Group
Participants in this group will not receive any intervention during the study period. They will be placed on a waiting list and instructed to refrain from any meditation or mindfulness-based activities until the study is completed. This group serves as a passive control to evaluate the effectiveness of the mindfulness-based intervention by comparing pre- and post-intervention measures.
No interventions assigned to this group
Interventions
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Mindfulness-Based Meditation (Integral Meditation - IM)
The intervention consists of 12 in-person mindfulness-based meditation sessions over a period of six weeks, with each session lasting one hour, twice per week. The practice, called Integral Meditation (IM), includes focused breathing, body relaxation, emotional awareness, and acceptance exercises.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Age ≥ 65 years
* No cognitive impairment, as measured by the Addenbrooke's Cognitive Examination (ACE-R)
Exclusion Criteria
* Substance dependence
65 Years
ALL
Yes
Sponsors
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University of Pavia
OTHER
Responsible Party
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Teresa Fazia
Principal Investigator
Locations
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University of Pavia
Pavia, , Italy
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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1Med_b
Identifier Type: -
Identifier Source: org_study_id
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