Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02400593
Other study ID # 14-1938
Secondary ID R01AG048811
Status Completed
Phase N/A
First received March 23, 2015
Last updated July 14, 2016
Start date August 2015
Est. completion date May 2016

Study information

Verified date July 2016
Source University of North Carolina, Chapel Hill
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review BoardUnited States: Federal Government
Study type Interventional

Clinical Trial Summary

Growing up in a low-income household has been shown to increase risk for, and susceptibility to many illnesses.The purpose of the study is to test an affective intervention for reversing biological risk factors, as related to childhood adversity, in midlife.

Participants will be asked to make two lab visits; attend six weekly, 1-hour meditation classes; as well as complete brief online daily surveys for 11 weeks, five biweekly surveys, and two 30-minute surveys prior to each lab visit. During the lab visits, participants will have their psychophysiology monitored for heart rate, blood pressure, respiration, and pulse. Participants will also have their blood drawn.

All surveys and questionnaires inquire about participants' current demographics, family history, perceptions about life and well-being, physical health, and monetary choices.


Recruitment information / eligibility

Status Completed
Enrollment 113
Est. completion date May 2016
Est. primary completion date May 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 35 Years to 64 Years
Eligibility Inclusion Criteria:

- fluent in written and spoken English

- have daily access to internet and a computer

Exclusion Criteria:

- engaged in regular meditation practice, either recently or in the past

- previously participated in a meditation study

- have allergies to adhesive materials (includes latex)

Study Design

Allocation: Randomized, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Behavioral:
Meditation Workshop
Six weeks of formal instruction in Lovingkindness or Mindfulness meditation.

Locations

Country Name City State
United States UNC PEP Lab Chapel Hill North Carolina

Sponsors (2)

Lead Sponsor Collaborator
University of North Carolina, Chapel Hill National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

References & Publications (5)

Cohen S, Doyle WJ, Turner RB, Alper CM, Skoner DP. Childhood socioeconomic status and host resistance to infectious illness in adulthood. Psychosom Med. 2004 Jul-Aug;66(4):553-8. — View Citation

Cole SW, Hawkley LC, Arevalo JM, Cacioppo JT. Transcript origin analysis identifies antigen-presenting cells as primary targets of socially regulated gene expression in leukocytes. Proc Natl Acad Sci U S A. 2011 Feb 15;108(7):3080-5. doi: 10.1073/pnas.1014218108. Epub 2011 Feb 7. — View Citation

Kok BE, Fredrickson BL. Upward spirals of the heart: autonomic flexibility, as indexed by vagal tone, reciprocally and prospectively predicts positive emotions and social connectedness. Biol Psychol. 2010 Dec;85(3):432-6. doi: 10.1016/j.biopsycho.2010.09.005. Epub 2010 Sep 22. — View Citation

Miller GE, Chen E, Fok AK, Walker H, Lim A, Nicholls EF, Cole S, Kobor MS. Low early-life social class leaves a biological residue manifested by decreased glucocorticoid and increased proinflammatory signaling. Proc Natl Acad Sci U S A. 2009 Aug 25;106(34):14716-21. doi: 10.1073/pnas.0902971106. Epub 2009 Jul 14. — View Citation

Miller GE, Chen E, Parker KJ. Psychological stress in childhood and susceptibility to the chronic diseases of aging: moving toward a model of behavioral and biological mechanisms. Psychol Bull. 2011 Nov;137(6):959-97. doi: 10.1037/a0024768. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in meditation time (Self-reported meditation time recorded daily) Self-reported meditation time recorded daily. Weeks 3, 4, 5, 6, 7, 8, 9 ,10, 11, 12 No
Secondary Leukocyte basal gene expression (evaluated through blood samples) Gene expression evaluated through blood samples. Week 0, Week 12 No
Secondary Levels of mistrust (Self-report questionnaire measure of hostility using 9-item Cooke-Medley scale) Self-report questionnaire measure of hostility using 9-item Cooke-Medley scale. Week 0, Week 12 No
Secondary Temporal Discounting (Monetary choice questionnaire to assess impulsive decision-making) Monetary choice questionnaire to assess impulsive decision-making. Week 0, Week 12 No
Secondary Cardiac vagal tone (Respiration and echocardiogram measured with respiration band and 2-lead electrode placement) Respiration and echocardiogram measured with respiration band and 2-lead electrode placement, respectively. Three-minute spontaneous breath followed by five minutes of paced breathing intervals. Week 0, Week 12 No
See also
  Status Clinical Trial Phase
Completed NCT01544270 - The Effects of Dietary Factors on Physiological Subjective Stress Responses N/A
Not yet recruiting NCT05501951 - Reduce High-risk Behaviours Under Chronic Stress Via tDCS-induced Neural Plasticity N/A
Completed NCT04431297 - Virtual Mindfulness Rounds in the Time of COVID-19 Pandemic N/A
Not yet recruiting NCT05789446 - Confirmatory Efficacy of the Building a Strong Identity and Coping Skills Program N/A
Terminated NCT01299402 - A Study on the Effects of Soulera Herbal Blend Intake on Chronic Stress in Healthy Adults Phase 1
Active, not recruiting NCT02764138 - Preventing Internalizing in Preadolescents Exposed to Chronic Stress N/A
Recruiting NCT06077097 - Traumatic Events in Childhood, Attachment, Pain Perception, Epigenetic Marks, Quality of Life and Resilience.