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Effects of Mindfulness Training on Chronic Inflammation in HIV-Infected Adults

Effects of Mindfulness Training on Chronic Inflammation in HIV-Infected Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02626949
Enrollment
84
Registered
2015-12-10
Start date
2016-03-31
Completion date
2017-12-18
Last updated
2022-05-09

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

Conditions

HIV

Keywords

HIV, AIDS, Mindfulness, Mindfulness-based stress reduction, Stress, Intervention, Inflammation

Brief summary

By 2015 half of the people living with HIV infection in the U.S. are estimated be over the age of 50, and this cohort of patients with well-controlled plasma viremia is aging at a more rapid pace than their non-HIV peers. Long-term chronic inflammation plays a critical role in premature aging in HIV-infected adults. Markers associated with chronic inflammation, including IL-6, CRP, sCD14 and d-dimer, have not only been shown to be present at higher levels in HIV-infected adults, but are also correlated to a wide variety of morbidities and mortality. The goal of this project is to determine the impact of two different interventions -- Mindfulness-Based Stress Reduction (MBSR) and Health Enhancement Program (HEP) -- on reducing biological markers associated with chronic inflammation in HIV-infected adults with an undetectable HIV viral load. In order to achieve this goal, a pilot RCT with 120 subjects over 50 years old who are on anti-retroviral therapy (ART) will be conducted with the following specific aims: 1) to assess the effect of MBSR and/or HEP on biomarkers of chronic inflammation (IL-6, CRP, sCD14, d-dimer), and, 2) to explore whether changes in psychological well-being (anxiety, depression, fatigue, cognitive functioning) mediate the impact on chronic inflammation. Subjects will be randomized to participation in a group MBSR course or to the HEP group both of which consist of 8 weekly sessions followed by 6 monthly booster sessions. Three time points will be measured: baseline, 8 weeks (immediately after completion of weekly intervention), and 6-months post-completion of weekly intervention. Mixed linear and structural equation model will be used to test the study hypotheses. The proposed study is innovative in that it is the first to explore the impact of a complementary mind-body intervention on chronic inflammation in HIV-infected adults. Given that the consequences of early aging in this cohort will be a burden on the health care system as well as a medical, social and psychological burden on those living with HIV, the study has the potential to have a major public health impact.

Detailed description

The proposed study will be the first to examine any form of alternative or complementary holistic therapy in older long-term HIV-infected persons with well-controlled plasma viremia. It will also be the first mind-body study of HIV-infected adults to be conducted using the most rigorous randomized controlled trial (RCT) design. From a translational medicine perspective, this study is innovative in that it examines a comprehensive set of biological markers specifically associated with chronic inflammation. No previous mind-body study has specifically targeted a set of biological markers that not only have been proven to be elevated in adults with HIV, but also been described as predictors of morbidity and overall mortality. This would be the first study to explore whether improvements in markers of psychosocial stress mediate the impact of the proposed interventions on chronic inflammation. This study is innovative in its effort to move HIV care beyond the current focus on virologic control, optimization of comorbid conditions, and encouragement of healthy lifestyle to include active interventions that can address the state of chronic inflammation and immune dysfunction underlying the early and accelerated aging process. Most bio-behavioral research in HIV to date has understandably focused on patients with poor adherence to HIV medication and treatment. This study is novel in its focus on highly adherent patients and the significant changes in profiles of biological markers associated with chronic inflammation documented in this cohort. The complementary medicine approach being studied has the potential to be integrated into the existing healthcare paradigm for HIV-positive persons. Specific Aims: Aim 1: To assess the effect of MBSR and HEP on biomarkers of chronic inflammation (IL-6, CRP, sCD14, d-dimer), in HIV-infected adults with well-controlled plasma viremia. Aim 2: To explore whether changes in markers of psychosocial well-being (anxiety, depression, fatigue, cognitive functioning) mediate the impact of these mind-body interventions on chronic inflammation. General Study Design: The proposed study is a prospective, randomized, clinical trial with attention control under the direction of the dual PIs, a behavioral scientist and a virologist. The study team is also made up of investigators from infectious diseases, mind-body medicine, geriatrics, and biostatistics. Subjects will be randomized to participation in an 8-week group MBSR course or to the Health Enhancement Program (HEP). The study population will consist of 120 individuals, 50 years old or older, long-term (5 years on ART or longer) HIV-infected adults with well-controlled plasma viremia and baseline IL-6 level of 1.17 pg/mL or greater. Randomization will be stratified to achieve balanced distribution between the groups based on gender and study site. One cohort group will participate in the 8-week MBSR course followed by six, once-per-month booster sessions, and separate cohort group will participate in HEP, with additional monthly educational meetings for six months. Both groups will be evaluated using two sets of measures: biological markers associated with chronic inflammation (IL-6, CRP, sCD14, d-dimer) and measures of psychosocial stress (anxiety, depression, fatigue, and mindfulness). Subjects will be assessed at three time points: baseline, 8 weeks (immediately after completion of weekly interventions), and 6-months post weekly courses (immediately after completion of booster sessions). The investigators will use mixed linear and structural equation model to test study hypotheses.

Interventions

BEHAVIORALMBSR Course

Formal mindfulness meditation methods taught in the MBSR course include: Body Scan Meditation (a supine meditation), Gentle Hatha Yoga (practiced with mindful awareness of the body), Sitting Meditation (mindfulness of breath, body, feelings, thoughts, and emotions), and Walking Meditation. Informal Mindfulness Meditation Practices (mindfulness in everyday life) include: 1) awareness of pleasant and unpleasant events, and, 2) deliberate awareness of routine activities and events such as eating, weather, walking, and interpersonal communication. Daily home assignments include a minimum of 30 minutes daily formal mindfulness practices and 5-15 minutes informal practice, 6 days per week for the entire duration of the course. Course sessions will consist of discussions oriented around weekly homework assignments, including an exploration of obstacles, and development of self-regulatory skills and capacities.

BEHAVIORALHEP Course

HEP is an active control that matches MBSR in non-specific factors, such as the amount of time participants interact, but does not include mindfulness practice as an active component. HEP instructors will be selected from experts in the areas covered: music, nutrition education, and, functional movement. The study's RC will coordinate HEP sessions and monitor attendance. Following the 8-week HEP protocol, subjects will meet monthly in 1.5-hour educational sessions to match the booster sessions of MBSR participants.

Sponsors

National Center for Complementary and Integrative Health (NCCIH)
CollaboratorNIH
Icahn School of Medicine at Mount Sinai
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* HIV-infected for 5 or more years * On ART for 5 or more years * HIV viral load consistently \<48 copies/mL for the last year * No anticipated changes in ART by provider or patient * Fluency in the English language * Age 45 years or older * Willingness to complete the entire MBSR or HEP interventions

Exclusion criteria

* Having participated in an MBSR course in the past * Current meditation and/or yoga practice * Began psychiatric medications in the past 2 months or plans to discontinue psychiatric medications * Currently receiving steroids or immunosuppressant drugs * Women who are pregnant or plan to become pregnant in the next year

Design outcomes

Primary

MeasureTime frameDescription
Interleukin 6 (IL-6) Biological MarkersBaseline, 8 weeks post intervention, and 6 months post interventionInterleukin 6 (IL-6) biological markers at 8 weeks and 6 months as compared to baseline.

Secondary

MeasureTime frameDescription
PROMIS - AnxietyBaseline, 8 weeks post intervention, and 6 months post interventionPatient Reported Outcomes Measurement Information System (PROMIS) - Anxiety - Measures of Psychosocial Stress, total scale 5-40 with higher score indicating more anxiety
PROMIS - FatigueBaseline, 8 weeks post intervention, and 6 months post interventionPatient Reported Outcomes Measurement Information System (PROMIS) - Fatigue - Measures of Psychosocial Stress, total scale 5-40 with higher score indicating more fatigue
BDI-IIBaseline, 8 weeks post intervention, and 6 months post interventionBeck Depression Inventory (BDI-II) - Measures of Psychosocial Stress, total scale from 0-63, with higher score indicating more depression
FFMQBaseline, 8 weeks post intervention, and 6 months post interventionThe Five Facet Mindfulness Questionnaire (FFMQ) - Measures of Mindfulness, full scale from 39 - 195, with higher score indicating more mindfulness
Retention Rates6 monthsAttendance records will provide retention rates.

Countries

United States

Participant flow

Pre-assignment details

114 were randomized prior to enrollment with final participants enrollment of 84.

Participants by arm

ArmCount
MBSR Course
Mindfulness-Based Stress Reduction Course (MBSR) consisting of 8 weekly sessions, 2 hours each, and a 5 hour silent retreat during the 6th week of the program.
40
HAEP Course
Health & Arts Enrichment Program (HAEP) consisting of 8 weekly sessions, 2 hours each, and 5 hour educational session during the 6th week of the program.
44
Total84

Withdrawals & dropouts

PeriodReasonFG000FG001
EnrolledLost to Follow-up76
EnrolledWithdrawal by Subject32
Randomization, Pre-Enrollmentdid not attend the baseline interview1511
Randomization, Pre-Enrollmentdid not meet inclusion criteria post-randomization13

Baseline characteristics

CharacteristicHAEP CourseTotalMBSR Course
Age, Continuous59.0 years
STANDARD_DEVIATION 7.4
58.3 years
STANDARD_DEVIATION 6.7
57.6 years
STANDARD_DEVIATION 5.9
Ethnicity (NIH/OMB)
Hispanic or Latino
15 Participants31 Participants16 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
29 Participants53 Participants24 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
26 Participants52 Participants26 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
18 Participants32 Participants14 Participants
Sex: Female, Male
Female
18 Participants37 Participants19 Participants
Sex: Female, Male
Male
26 Participants47 Participants21 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 400 / 44
other
Total, other adverse events
0 / 400 / 44
serious
Total, serious adverse events
0 / 400 / 44

Outcome results

Primary

Interleukin 6 (IL-6) Biological Markers

Interleukin 6 (IL-6) biological markers at 8 weeks and 6 months as compared to baseline.

Time frame: Baseline, 8 weeks post intervention, and 6 months post intervention

Population: One participant did not have data for baseline. Data for those participants who completed the 8 weeks and 6 months post-intervention included.

ArmMeasureGroupValue (MEDIAN)
MBSR CourseInterleukin 6 (IL-6) Biological MarkersBaseline2.24 pg/mL
MBSR CourseInterleukin 6 (IL-6) Biological Markers8 weeks (post intervention)2.53 pg/mL
MBSR CourseInterleukin 6 (IL-6) Biological Markers6 months (post intervention)2.89 pg/mL
HAEP CourseInterleukin 6 (IL-6) Biological Markers8 weeks (post intervention)2.88 pg/mL
HAEP CourseInterleukin 6 (IL-6) Biological MarkersBaseline2.63 pg/mL
HAEP CourseInterleukin 6 (IL-6) Biological Markers6 months (post intervention)2.62 pg/mL
Secondary

BDI-II

Beck Depression Inventory (BDI-II) - Measures of Psychosocial Stress, total scale from 0-63, with higher score indicating more depression

Time frame: Baseline, 8 weeks post intervention, and 6 months post intervention

Population: Data for those participants who completed the 8 weeks and 6 months post-intervention included.

ArmMeasureGroupValue (MEAN)Dispersion
MBSR CourseBDI-IIBaseline15.0 score on a scaleStandard Deviation 10
MBSR CourseBDI-II8 weeks post intervention9.7 score on a scaleStandard Deviation 9.8
MBSR CourseBDI-II6 months post intervention9.7 score on a scaleStandard Deviation 7.8
HAEP CourseBDI-IIBaseline15.6 score on a scaleStandard Deviation 10.6
HAEP CourseBDI-II8 weeks post intervention14.7 score on a scaleStandard Deviation 10.6
HAEP CourseBDI-II6 months post intervention13.1 score on a scaleStandard Deviation 11.7
Secondary

FFMQ

The Five Facet Mindfulness Questionnaire (FFMQ) - Measures of Mindfulness, full scale from 39 - 195, with higher score indicating more mindfulness

Time frame: Baseline, 8 weeks post intervention, and 6 months post intervention

Population: Data for those participants who completed the 8 weeks and 6 months post-intervention included.

ArmMeasureGroupValue (MEAN)Dispersion
MBSR CourseFFMQBaseline135.7 score on a scaleStandard Deviation 21.8
MBSR CourseFFMQ8 weeks post intervention144.3 score on a scaleStandard Deviation 18.6
MBSR CourseFFMQ6 months post intervention145.3 score on a scaleStandard Deviation 19.2
HAEP CourseFFMQBaseline135.4 score on a scaleStandard Deviation 19.8
HAEP CourseFFMQ8 weeks post intervention134.7 score on a scaleStandard Deviation 22.3
HAEP CourseFFMQ6 months post intervention141.5 score on a scaleStandard Deviation 23
Secondary

PROMIS - Anxiety

Patient Reported Outcomes Measurement Information System (PROMIS) - Anxiety - Measures of Psychosocial Stress, total scale 5-40 with higher score indicating more anxiety

Time frame: Baseline, 8 weeks post intervention, and 6 months post intervention

Population: Data for those participants who completed the 8 weeks and 6 months post-intervention included.

ArmMeasureGroupValue (MEAN)Dispersion
MBSR CoursePROMIS - Anxiety8 weeks post intervention15.1 score on a scaleStandard Deviation 6.6
MBSR CoursePROMIS - AnxietyBaseline18.7 score on a scaleStandard Deviation 8.2
MBSR CoursePROMIS - Anxiety6 months post intervention15.9 score on a scaleStandard Deviation 6.9
HAEP CoursePROMIS - AnxietyBaseline19.3 score on a scaleStandard Deviation 6.9
HAEP CoursePROMIS - Anxiety8 weeks post intervention18.4 score on a scaleStandard Deviation 7.4
HAEP CoursePROMIS - Anxiety6 months post intervention18.5 score on a scaleStandard Deviation 7.5
Secondary

PROMIS - Fatigue

Patient Reported Outcomes Measurement Information System (PROMIS) - Fatigue - Measures of Psychosocial Stress, total scale 5-40 with higher score indicating more fatigue

Time frame: Baseline, 8 weeks post intervention, and 6 months post intervention

Population: Data for those participants who completed the 8 weeks and 6 months post-intervention included.

ArmMeasureGroupValue (MEAN)Dispersion
MBSR CoursePROMIS - FatigueBaseline21.2 score on a scaleStandard Deviation 8.1
MBSR CoursePROMIS - Fatigue8 weeks post intervention16.8 score on a scaleStandard Deviation 7.7
MBSR CoursePROMIS - Fatigue6 months post intervention18.8 score on a scaleStandard Deviation 8
HAEP CoursePROMIS - FatigueBaseline21.4 score on a scaleStandard Deviation 9.4
HAEP CoursePROMIS - Fatigue8 weeks post intervention21.1 score on a scaleStandard Deviation 8.1
HAEP CoursePROMIS - Fatigue6 months post intervention19.3 score on a scaleStandard Deviation 9.6
Secondary

Retention Rates

Attendance records will provide retention rates.

Time frame: 6 months

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
MBSR CourseRetention Rates30 Participants
HAEP CourseRetention Rates36 Participants

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