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Protocol for a randomized controlled trial of mindfulness-based stress reduction to improve attentional control in older adults (HealthyAgers trial).

BMC geriatrics
January 1, 1970
Ruchika Shaurya Prakash et al. (13 authors)
Clinical Trial ProtocolJournal ArticleHuman StudyClinical
Study Details

Study Goal

The researchers aimed to determine the efficacy of a mindfulness-based stress reduction program in improving attentional control and reducing mind-wandering in older adults.

Results Summary

The study design suggests potential benefits of mindfulness for attentional control and mind-wandering, with secondary outcomes including improved cognition, emotion regulation, and inflammation markers, but final results are pending as it is a trial in progress.

Population

Older adults aged 65-85 years.

Effective Dosage

Eight-week mindfulness program (specific frequency not detailed).

Duration

Eight weeks, with booster sessions every three months for 12 months.

Interactions

None mentioned

Extracted Claims (5)
InterventionDirectionEndpointPopulationDosageImpactClaim #
mindfulness meditation
decrease
age-related declines in cognitive functioning
-
-
reduce
#1
mindfulness meditation
increase
affective health
-
-
improve
#2
mindfulness meditation
increase
neural circuitry supporting improved cognitive and affective health
-
-
strengthen
#3
mindfulness-based stress reduction program
increase
attentional control
older adults
-
improving
#4
mindfulness-based stress reduction program
decrease
mind-wandering
older adults
-
reducing
#5
Abstract

BACKGROUND: Mindfulness meditation is a form of mind-body intervention that has increasing scientific support for its ability to reduce age-related declines in cognitive functioning, improve affective health, and strengthen the neural circuitry supporting improved cognitive and affective health. However, the majority of existent studies have been pilot investigations with small sample sizes, limited follow-up data, and a lack of attention to expectancy effects. Here, we present the study design of a Phase I/II, efficacy trial-HealthyAgers trial-that examines the benefits of a manualized mindfulness-based stress reduction program in improving attentional control and reducing mind-wandering in older adults. METHODS: One hundred fifty older adults (ages 65-85 years) will be randomized into one of two groups: an eight-week mindfulness program or an eight-week, placebo-controlled, lifestyle education program. Behavioral and neuroimaging assessments are conducted before and after the training. Participants are then invited to booster sessions once every three months for a period of 12 months with post-intervention follow-up assessments conducted at 6-months and 12-months. The primary outcomes for the study are behavioral measures of attentional control and mind-wandering. Additional, secondary outcomes include network strength in an a priori defined neuromarker of attentional control, fluid and everyday cognition, emotion regulation strategy use, and markers of inflammation. DISCUSSION: This study will establish the efficacy of a group-based, low-cost mind-body intervention for the inter-related facets of attentional control and mind-wandering in older adults. Strengths of this study include a well-designed, placebo-controlled comparison group, use of web/mobile application to track study adherence, and longitudinal follow-up. TRIAL REGISTRATION: Clinicaltrials.gov (# NCT03626532 ). Registered August 4, 2018.

Medical Subject Headings (MeSH)
AgedAged, 80 and overAttentionClinical Trials, Phase I as TopicClinical Trials, Phase II as TopicHumansMindfulnessRandomized Controlled Trials as TopicResearch DesignStress, Psychological
Study Links
Quality Scores
SafetyNot Assessed
Efficacy75/10
Quality85/10
Citation Metrics
Total Citations4
Citations/Year1.3
Relative Citation Ratio0.65
NIH Percentile34.9%
Research Impact Scores
APT Score0.05
Weight Score1.61
Normalized Score0.67
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