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Mindfulness-based Short Intervention for Seniors - Decentering Effects on Cognitive Functions and Psychological Distress

Mindfulness-based Short Intervention for Seniors - Decentering Effects on Cognitive Functions and Psychological Distress

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04165005
Enrollment
30
Registered
2019-11-15
Start date
2017-11-01
Completion date
2018-08-01
Last updated
2019-11-15

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

Conditions

Cognitive Change, Old Age; Debility, Psychological Distress

Keywords

elderly, MBSR, cognitive functions, psychological status

Brief summary

The present study examined the effect of a short Mindfulness-based intervention emphasizing a 'decentering' component on elderly seniors. Methods: 30 community seniors (Mage= 74.7) performed either 'decentering' intervention, guided imagery intervention, or control care as usual. The 8-week interventions included weekly 20-minute sessions and daily 10-minute home practice. Participants underwent a cognitive and emotional assessment before and after the interventions, which included filling out questionnaires and performing the Simon task. Trial registration: The study follows the principles of the Declaration of Helsinki, approved by the committee in Beer-Yaacov Hospital, Israel (number 579) on 24 Oct. 2017.

Interventions

BEHAVIORALdecentering

examined a mindfulness-based intervention focused on a decentering component, that is suitable for elders, aimed to influence on cognitive measures and psychological distress.

BEHAVIORALguided imagery

relaxing guided imagery including breathing exercises.

Sponsors

Ruppin Acdemic Center
CollaboratorOTHER
Ben-Gurion University of the Negev
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Investigator)

Eligibility

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

Inclusion criteria

* age 65 and above * membership in the study's specific enrollment community centers * scoring 24 and above in the Mini-Mental State Examination (MMSE).

Exclusion criteria

* age under 65 * not being a member in the study's specific enrollment community centers * scoring under 24 in the Mini-Mental State Examination (MMSE).

Design outcomes

Primary

MeasureTime frameDescription
Simon task- change from baseline to after interventionat baseline and through intervention's completion, 10 weeks.a cognitive task, assessing control processes under speeded conditions, measured by response time and accuracy rate. shorter response time and higher accuracy rate indicate better performance.

Secondary

MeasureTime frameDescription
FFMQ- change from baseline to after interventionat baseline and through intervention's completion, 10 weeks.The Five-Fact Mindfulness Questionnaire, a manipulation check of mindfulness, ranging from 1 to 5, with higher score indicating higher mindfulness level
PWB questionnaire- change from baseline to after interventionat baseline and through intervention's completion, 10 weeks.The Psychological Well-Being Questionnaire, ranging from 1 to 6, with higher score indicating higher well-being level
MMSE- change from baseline to after interventionat baseline and through intervention's completion, 10 weeks.the Mini-Mental State examination: a cognitive function measure for elders, used to determine participation eligibility. the animation score ranges between 0 to 30, with higher score indicating better cognitive functioning
PHQ-9- change from baseline to after interventionat baseline and through intervention's completion, 10 weeks.The Patient Health Questionnaire - a depression levels measure, ranging from 0 to 3, with higher score indicating higher depression level
BDI-II- change from baseline to after interventionat baseline and through intervention's completion, 10 weeks.The Beck Depression Inventory-II- a depression levels measure, ranging from 1 to 4, with higher score indicating higher depression level

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026