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Stress Reduction Training to Improve Sleep Quality, Stress Physiology & Cardiovascular Disease (CVD) Risk Markers

The Effect of Mindfulness-Based Stress Reduction on Sleep Quality, Stress Physiology & CVD Risk

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01343810
Enrollment
87
Registered
2011-04-28
Start date
2010-09-30
Completion date
2013-10-31
Last updated
2014-03-10

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

Conditions

Stress, Psychological, Sleep, Inflammation, Cardiovascular Diseases

Keywords

Mindfulness-Based Stress Reduction, Meditation, Psychological stress, Sleep quality, Cardiovascular disease, Inflammation

Brief summary

The goal of this study is to better understand the potential value of reducing stress to ameliorate a cluster of biological and behavioral factors implicated in cardiovascular disease (CVD) risk. These factors include psychological distress, poor sleep quality, and exaggerated physiological responses to emotional stress. Results will be used to develop an innovative brief intervention to reduce risk for CVD by improving sleep quality, ameliorating psychological distress, and attenuating stress physiology.

Detailed description

This study will be conducted among 200 men and women participating in 8-week Mindfulness-Based Stress Reduction (MBSR) classes at Duke Integrative Medicine in Durham, North Carolina. The central hypothesis of this NIH-funded clinical trial (R00 AT004945, PI: Greeson) is that mindfulness meditation training is associated with increased levels of mindfulness and improved cognitive-emotional functioning that, together, are associated with reduced psychological distress, improved sleep quality, and less exaggerated physiological responses to emotional stress, including blood pressure and inflammation. This study is designed to examine psychological and biological mechanisms that may explain individual differences in MBSR outcomes. This knowledge is important because it will help us better understand who is most likely to benefit from mindfulness meditation training, and why. The results from this study are expected to elucidate mechanisms underlying the mental and physical health benefits of stress reduction, which can help guide clinicians in referring the most suitable patients to local MBSR programs.

Interventions

The MBSR program consists of 8 weekly classes that last for 2.5 hours each and a commitment to daily meditation practice for the duration of the course. Classes include didactic instruction on mindfulness and its relationship to stress and health, guided meditation practices, and group discussion. Mindfulness meditation practices include awareness of breathing, awareness of emotions, body scan, mindful hatha yoga, mindful walking, mindful eating, mindful listening, and lovingkindness (metta). Participants are expected to practice formal meditation outside of class for 20-45 min per day, 6 days per week. In addition, participants are encouraged apply mindfulness to everyday activities like eating, communicating with others, and hobbies. Written materials and audio CDs with guided meditations and yoga are provided. The course also includes one full day (7-hours) of meditation on a Saturday following the 6th week of class.

BEHAVIORALMindfulness-Based Stress Reduction (MBSR)

The MBSR program consists of 8 weekly classes that last for 2.5 hours each and a commitment to daily meditation practice for the duration of the course. Classes include didactic instruction on mindfulness and its relationship to stress and health, guided meditation practices, and group discussion. Mindfulness meditation practices include awareness of breathing, awareness of emotions, body scan, mindful hatha yoga, mindful walking, mindful eating, mindful listening, and lovingkindness (metta). Participants are expected to practice formal meditation outside of class for 20-45 min per day, 6 days per week. In addition, participants are encouraged apply mindfulness to everyday activities like eating, communicating with others, and hobbies. Written materials and audio CDs with guided meditations and yoga are provided. The course also includes one full day (7-hours) of meditation on a Saturday following the 6th week of class.

Sponsors

National Center for Complementary and Integrative Health (NCCIH)
CollaboratorNIH
Duke University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

1. Willing to participate in an 8 week stress reduction training program 2. Between 18 and 65 years old 3. Generally in good health and not taking medication 4. Able to speak and read English 5. Willing to provide informed consent 6. Able to access the internet 7. Able to attend 4 study visits at Duke University Medical Center

Exclusion criteria

1. Younger than 18 years old/Older than 65 2. Asthma 3. Allergies 4. Arthritis 5. Autoimmune disease (Lupus) 6. Cancer 7. Cardiovascular disease, heart attack, or atherosclerosis 8. Diabetes or High Blood Sugar (\>124 mg/dl) 9. Hypertension or high blood pressure (140/90 mmHg) 10. High cholesterol (\>240 mg/dl) 11. Obesity (Body Mass Index \>30) 12. Irritable Bowel Syndrome (IBS) 13. Mitral Valve Prolapse, or Heart Murmurs 14. Irregular Menstrual Cycles (Peri-Menopause Excluded. Menopause may be included.) 15. Skin conditions, such as eczema or psoriasis (acne may be included) 16. Sleep Apnea 17. Depression, anxiety, substance use, or any other mental health diagnosis 18. Sleep aids like Tylenol PM or Ambien on a regular basis 19. Medication for allergies or asthma on a regular basis 20. Aspirin or baby Aspirin on a regular basis 21. Oral contraceptives or birth control (women only) 22. Hormone Replacement Therapy 23. Flu shot within past 3 weeks 24. Underweight (BMI \< 18.5) 25. Current smoker 26. \>1 alcoholic drink/day (women)/ \>2 alcoholic drinks/day (men) 27. Hospitalized within the last 3 months 28. Treated for any infections within the last 3 months 29. Current meditation practice \>1x/month 30. Previously taken a Mindfulness-Based Stress Reduction (MBSR) course 31. Participation in any other research studies in the past year that involved drugs or taking blood 32. Recently donated blood. (500 cc's in last 8 wks)

Design outcomes

Primary

MeasureTime frameDescription
Sleep qualityBaseline, post-intervention (2 months), follow-up (8 months)Sleep quality will be assessed using 3 different methods: daily sleep diaries, questionnaires and actigraphy.
Stress physiologyBaseline, post-intervention (2 months), follow-up (8 months)Physiological responses to mild emotional stress (5-minute Anger Recall Task) will be assessed in the laboratory before and after participating in an 8-week Mindfulness-Based Stress Reduction (MBSR) program. During the stress testing sessions, we will take measures of heart rate, blood pressure, stress hormones, metabolism, inflammation, emotions, and mindful qualities.

Secondary

MeasureTime frameDescription
Negative AffectBaseline, post-intervention (2 months), follow-up (8 months)Anxiety; anger; depressive symptoms.
Cognitive functioningBaseline, post-intervention (2 months), follow-up (8 months)Cognitive abilities and concerns, including attention, concentration, memory, organization, and clarity of thinking.
MindfulnessBaseline, post-intervention (2 months), follow-up (8 months)Mindful qualities, including observing, describing, non-judging, non-reactivity, acting with awareness, mindfulness, self-kindness, and common humanity.
Stress-related physical symptomsBaseline, post-intervention (2 months), follow-up (8 months)Common physical symptoms associated with stress, including muscle tension, gastrointestinal complaints, headaches, etc.
Emotion regulationBaseline, post-intervention (2 months), follow-up (8 months)Rumination; avoidance; suppression; reappraisal.
Health-related quality of lifeBaseline, post-intervention (2 months), follow-up (8 months)Global health rating; physical functioning; fatigue; satisfaction with social role; pain intensity and pain-related interference with daily activities.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026