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Mindfulness Training: the Effects of a Stress Reduction Program on Older Portuguese-speaking People in Luxembourg

Mindfulness Training in Aging: the Effects of a Stress Reduction Program on Portuguese-speaking People Aged Fifty-five and Over Residing in Luxembourg

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05615337
Acronym
MEDITAGING
Enrollment
89
Registered
2022-11-14
Start date
2022-04-26
Completion date
2023-08-31
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Aging, Mindfulness

Brief summary

This project aims to investigate the MBSR feasibility and its effects in old Portuguese-speaking adults living in Luxemburg. This study will be a two-arm randomized-double blinded-controlled study, including 90 healthy older adults. The MBSR will be conducted in groups over a total of eight weeks, incorporating weekly meetings, a retreat of 4 hours, and extra activities to be practiced at home. The active control condition will be a program with different components such as painting, nutrition information, physical activity, cognitive enhancement, risk factors for dementia, and health promotion. Neuropsychological assessments will be conducted at baseline, immediately after and one-month post-intervention. The researchers will also do pre-post salivary cortisol and resting heart rate variability analyses, as surrogate measures to assess stress level.

Interventions

BEHAVIORALMBSR

The MBSR is an eight-week group-based psychoeducational program. It is performed in weekly group sessions with the duration of 2.5 hours and a half-day retreat of 4 hours. The program involves focused attention, consisting of body scan, yoga, and meditation. This program trains participants to be attentive to their thoughts, emotions, and sensations. There are also discussions on relevant topics related to the physiology of stress and strategies of coping. Materials for home practice are provided.

BEHAVIORALHPP

The HPP has the same structure of MBSR, including different components such as music, nutrition, cognitive enhancement, risk factors for dementia, and physical activity. During the half-day retreat participants are involved in watercolor painting activities. Materials for home practice are also provided.

Sponsors

Luxembourg National Research Fund (FNR)
CollaboratorUNKNOWN
University of Luxembourg
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Portuguese-speaker Migrants over 55 years old, residing in the Grand-Duchy of Luxembourg the Greater Region; * Mastery of written and spoken Portuguese; * Subjects without cognitive impairment (The Mini Mental State Examination - MMSE, cut-off of \< 22 will be adopted since most of participants are expected to have low education level -Kochhann et al, 2010) * Subjects with a full capacity of consent.

Exclusion criteria

* Previous (up to 2 years before) or actual weekly participation in formal meditation, yoga or mindfulness-based interventions * Concomitant participation in other kind of enhancement intervention in group, e.g., cognitive training, psychological therapy * Severe hearing or visual impairment (not corrected) * Severe medical condition requiring intensive medical care that makes it difficult to participate in the group sessions * Refusal to sign the informed consent * Diagnosis of dementia * Clinical neurodegenerative illness, psychotic disorder, unstable psychiatric condition which makes it difficult to participate in groups, posttraumatic stress disorder or history of trauma, individuals with acute psychosis, mania, suicidality or alcohol chronic or other substance abuse within the last 6 months (cutoff: 2 points at the Adult DSM-5 Self-Rated Level 1 Cross-Cutting Symptom Measure)

Design outcomes

Primary

MeasureTime frameDescription
Changes in executive functioning comparing the two groups over timeT1- baseline before the intervention; T2 - 8 weeks after baseline; T3 - 1 month after the interventionAssessed by the Trail Making Test

Secondary

MeasureTime frameDescription
Qualitative interview comparing the two groups over timeT1- baseline before the intervention; T2 - 8 weeks after baseline; T3 - 1 month after the interventionInterview asking about the program challenges and benefits
Changes in the dispositional mindfulness comparing the two groups over timeT1- baseline before the intervention; T2 - 8 weeks after baseline; T3 - 1 month after the intervention. Minimum value: 15. Maximum value: 90. Higher scores reflect greater mindfulness.The Mindfulness Attention and Awareness Scale (MAAS)
Change in stress levels comparing the two groups over timeT1- baseline before the intervention; T2 - 8 weeks after baseline; T3 - 1 month after the intervention. Minimum value: 0. Maximum value: 40. Higher scores reflect greater perceived stress.Assessed by the Perceived Stress Scale
Changes in cortisol levels comparing the two groups over timeT1- baseline before the intervention; T2 - 8 weeks after baselineassessed by collecting saliva at baseline and post-intervention
Change in sleep quality comparing the two groups over timeT1- baseline before the intervention; T2 - 8 weeks after baseline; T3 - 1 month after the interventionPittsburgh sleep quality index
Changes in general cognition comparing the two groups over timeT1- baseline before the intervention; T2 - 8 weeks after baseline; T3 - 1 month after the interventionMini-Mental State Questionnaire
Changes in humor between the two groups over timeT1- baseline before the intervention; T2 - 8 weeks after baseline; T3 - 1 month after the interventionGeriatric Anxiety Inventory (GAI)
Change in the heart rate assessment comparing the two groups over timeT1- baseline before the intervention; T2 - 8 weeks after baseline; T3 - 1 month after the interventionHeart rate variability

Countries

Luxembourg

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026