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Effect of Mindfulness Training on Sleep and Inflammation Among Older Adults With Sleep Problems

A Randomized Controlled Trial Testing the Effect of Mindfulness Practices Versus Sleep Education on Sleep and Inflammation Among Older Adults With Sleep Problems

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01534338
Acronym
MAPS
Enrollment
48
Registered
2012-02-16
Start date
2012-02-29
Completion date
2012-12-31
Last updated
2012-12-11

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

Conditions

Inflammation, Sleep Problems

Keywords

Sleep, inflammation, mindfulness, meditation, randomized controlled trial

Brief summary

The primary aim of the study is to test the effect of mindfulness training on sleep parameters among older adults with insomnia symptoms The secondary aims are to examine if changes in mindfulness meditation practice (daily log) and level of mindfulness (self-report) are associated with changes in sleep parameters, and to determine if mindfulness training is associated with in vitro biological markers of peripheral inflammation

Interventions

BEHAVIORALMindfulness Meditation

Participants will attend weekly 2-hour classes for a total of 6 weeks and participants will monitor their sleep with a daily sleep diary.

BEHAVIORALSleep Education

Participants will attend weekly 2-hour classes for a total of 6 weeks and participants will monitor their sleep with a daily sleep diary.

Sponsors

University of California, Los Angeles
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Men and women (all races and ethnicities) 55 years of age and older * Have current problems sleeping * Fluent in English * Able to understand and provide signed informed consent * Willing to be randomly assigned to treatment condition

Exclusion criteria

* Individuals currently undergoing major medical treatment such as surgery, radiation, or immunotherapy * Individuals living outside of a 20 mile radius from the UCLA Medical Center * Individuals with current substance dependence

Design outcomes

Primary

MeasureTime frameDescription
SleepWithin 2 weeks post-interventionPrimary sleep outcomes to be assessed include Daily sleep diary, Pittsburgh Sleep Quality Index, Fatigue Symptom Inventory, Insomnia Severity Index, and Pre-Sleep Arousal Scale

Secondary

MeasureTime frameDescription
MindfulnessWithin 2 weeks post-interventionMindfulness will be assessed by self report with the Five Facet Mindfulness Questionnaire and a daily log of amount of mindfulness practice
Inflammatory BiologyWithin 2 weeks post-interventionPro-inflammatory cytokines and associated transcription markers will be assessed with in vitro assay of peripheral blood via venipuncture collected between 9am and 1130am

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026