Staying Well: A Clinical Trial of Mindfulness-Based Stress Reduction and Education Groups for HIV
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Purpose
To examine the effects of Mindfulness-Based Stress Reduction (MBSR) and education groups on HIV (Human Immunodeficiency Syndrome) infection. Key outcomes include CD4 and viral load, stress hormones, depression and quality of life.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV |
Behavioral: Mindfulness-Based Stress Reduction (MBSR) Behavioral: HIV-education and self-management workshop |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Mindfulness-Based Stress Reduction (MBSR), Stress Arousal and Immune Response in Early HIV |
- Change in CD4 T-cell Count [ Time Frame: baseline to 12 months ] [ Designated as safety issue: No ]
- Change in Depression as Measured by Beck Depression Inventory (BDI) [ Time Frame: baseline to 12 months ] [ Designated as safety issue: No ]The BDI is a widely used outcome measure for studies of depression. The BDI consists of 21 items that are rated on a 4-point scale according to how severely they are experienced. Scores range from 0-63, with higher scores reflecting greater depression.
- Change in Perceived Stress as Measured by Perceived Stress Scale (PSS) [ Time Frame: baseline to 12 months ] [ Designated as safety issue: No ]Perception of stress was measured with the 10-item version of the Perceived Stress Scale. This widely used measure of perceived stress was designed to tap how unpredictable, uncontrollable, and overloaded respondents find their lives. Participants rate how often they felt or thought a certain way over the past month on a 4-point scale (0 = Never, 4 = Very Often). Scores range from 0-40, with higher scores reflecting greater perceived stress.
- Change in Positive and Negative Affect (PANAS) Positive Affect (PA) Score [ Time Frame: baseline to 12 months ] [ Designated as safety issue: No ]Emotion was assessed with the Positive and Negative Affect Schedule (PANAS). The PANAS measures intensity of positive and negative emotions over the past week. The scale consists of 20 items--10 positive and 10 negative emotions. Respondents are asked to indicate how strongly they felt each emotion on a scale from 0 to 4 (not at all to extremely). The Positive Affect (PA) score is derived from summing the scores on the 10 positive emotions. Scores on the PA subscale range from 0-40, with higher scores reflecting more positive affect over the past week.
- Change in Positive and Negative Affect Scale (PANAS) Negative Affect (NA) Score [ Time Frame: baseline to 12 months ] [ Designated as safety issue: No ]Emotion was assessed with the Positive and Negative Affect Schedule (PANAS\). The PANAS measures intensity of positive and negative emotions over the past week. The scale consists of 20 items--10 positive and 10 negative emotions. Respondents are asked to indicate how strongly they felt each emotion on a scale from 0 to 4 (not at all to extremely). The Negative Affect (NA) score is derived from summing the scores on the 10 negative emotions. Scores on the NA subscale range from 0-40, with higher scores reflecting more negative affect over the past week.
- Change in Depression as Measured by the Patient Health Questionnaire-9 (PHQ-9) [ Time Frame: baseline to 12 months ] [ Designated as safety issue: No ]We used the Patient Health Questionnaire (PHQ-9) as a measure of depressive symptom severity. The PHQ-9 is the depression module of the self-administered version of the Primary Care Evaluation of Mental Disorders (PRIME-MD) diagnostic instrument. Participants rate the frequency of 9 depression symptoms over the past 2 weeks from 0 (not at all) to 3 (nearly every day). Scores range from 0 to 27, with higher scores reflecting greater severity of depressive symptoms.
- Quality of Life (Short Form Health Survey; SF-36); Cortisol (Basal a.m. and Diurnal Change); T-cell Activation (i.e. CD38-cell Surface Marker) and NK Cell Number and Function; Autonomic Nervous System Activity ; Cell Aging [ Time Frame: 3, 6, and 12 months ] [ Designated as safety issue: No ]
| Enrollment: | 177 |
| Study Start Date: | May 2005 |
| Study Completion Date: | September 2009 |
| Primary Completion Date: | September 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 0
Mindfulness Based Stress Reduction (MBSR)
|
Behavioral: Mindfulness-Based Stress Reduction (MBSR)
8 week MBSR course
Other Name: Mindfulness meditation
|
|
Active Comparator: 1
HIV education/self-management workshop
|
Behavioral: HIV-education and self-management workshop
8-week group covering a variety of educational topics about managing HIV infection.
|
Detailed Description:
Stress and depression are associated with more rapid loss of CD4 cells in HIV infection. Interventions that slow the advance of HIV infection and delay the introduction of antiretroviral therapy (ART) could make an important contribution to HIV management in both the developed and developing world. We are conducting a 330 person randomized, controlled clinical trial of MBSR for persons with HIV-1 infection and CD4 T-lymphocyte counts > 250 cells/µm who are not on antiretroviral therapy. Participants are randomized in a 1:1 distribution to either the MBSR intervention or to an education group that will control for the attention and social interaction aspects of MBSR. Participants are evaluated at 0, 3, 6 and 12 months. Key outcome measures at 12 months include differences in CD4 T cell counts, HIV viral load, perceived stress, depression, and positive affect. We are also examining whether MBSR is associated with changes in neuroendocrine function (autonomic nervous system activity, cortisol secretion) and alterations in immune function that may serve as intermediate steps between the neuroendocrine effects of MBSR and CD4 T cell counts, such as changes in T cell activation. A subset of 90 participants will be studied in additional detail using a structured laboratory stress challenge.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- HIV+
- Viral Load>100
- CD4 T-Cells>250
- Not on Antiretroviral therapy (ART)
- Ability to Speak English
- Stable address/living situation
Exclusion Criteria:
- Inability to provide informed consent
- Use of ART within the past 120 days
- Any substance abuse,mental health or medical condition that the opinion of the Principal Investigator (PI) would make it difficult for the potential participant to participate in the intervention
- Plans to start ART in the next 12 months
- Previous MBSR training and/or current practice
- Current use or use in past 6 months (mos.) of chemotherapy or immunomodulator drugs, including oral steroids or plans to start in the next 12 mos.
- Initiation of new class of psychiatric medication in past 2 months.
Contacts and Locations| United States, California | |
| Osher Center for Integrative Medicine | |
| San Francisco, California, United States, 94143-1726 | |
| Principal Investigator: | Frederick M. Hecht, M.D. | University of California, San Francisco |
| Study Director: | Susan Folkman, PhD | University of California, San Francisco |
More Information
No publications provided
| Responsible Party: | University of California, San Francisco |
| ClinicalTrials.gov Identifier: | NCT00271856 History of Changes |
| Other Study ID Numbers: | P01 AT002024, P01AT002024 |
| Study First Received: | December 30, 2005 |
| Results First Received: | August 3, 2011 |
| Last Updated: | April 11, 2012 |
| Health Authority: | United States: Federal Government |
Keywords provided by University of California, San Francisco:
|
HIV Meditation Stress Randomized Controlled Trial |
Complementary Therapies MBSR Not on ART medications |
ClinicalTrials.gov processed this record on May 21, 2013