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A Randomized Controlled Trial of a Mindfulness-Based Stress Reduction Intervention for Men Living With HIV

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
MBSR group
Control
Sponsored by
Mount Sinai Hospital, Canada
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Mindfulness, HIV, Male, Living with HIV, 18-70 years of age, live within one hour of hospital, fluent in English, Complementary Therapies, HIV Therapeutic Vaccine

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Male
  • Living with HIV
  • 18-70 years of age
  • Fluent in English
  • Lives within one hour of the hospital

Exclusion Criteria:

  • Severe depression
  • Current suicide ideation
  • Substance abuse
  • Impaired cognitive function

Sites / Locations

  • Mount Sinai Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

Participants in the first arm participate in an 8-week MBSR group

Participants assigned to the control arm do not receive the MBSR program but may or may not be receiving current psychotherapy or counselling

Outcomes

Primary Outcome Measures

Subjects in the MBSR group will have greater improvement in measures of psychosocial functioning (i.e. anxiety, depression, HIV-related distress, affectivity) at 8 weeks and 6-months post-intervention
Subjects in the MBSR group will demonstrate significantly greater improvement on measures of worry and rumination at 8 weeks and 6-months post-intervention
MBSR will result in greater improvement in pain compared to the control arm

Secondary Outcome Measures

Reductions in anxiety and depression during MBSR will be moderated by reductions in worry and ruminations, respectively

Full Information

First Posted
September 11, 2007
Last Updated
October 2, 2007
Sponsor
Mount Sinai Hospital, Canada
Collaborators
Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Canadian Foundation for AIDS Research (CANFAR)
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1. Study Identification

Unique Protocol Identification Number
NCT00529971
Brief Title
A Randomized Controlled Trial of a Mindfulness-Based Stress Reduction Intervention for Men Living With HIV
Official Title
A Randomized Controlled Trial of a Mindfulness-Based Stress Reduction Intervention for Men Living With HIV
Study Type
Interventional

2. Study Status

Record Verification Date
September 2007
Overall Recruitment Status
Completed
Study Start Date
December 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Mount Sinai Hospital, Canada
Collaborators
Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Canadian Foundation for AIDS Research (CANFAR)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will examine the effectiveness of Mindfulness-Based Stress Reduction (MBSR) in helping men living with HIV cope with negative emotions and stresses in their life. MBSR is an approach to reducing stress for patients with chronic medical conditions. It involves systematic training in mindfulness meditation practices to increase quality of life and to reduce general stress, anxiety, depression or pain. The effectiveness of MBSR will be evaluated by looking at changes in participants' experience of stress, anxiety associated with pain management and psychosocial functioning before and after they receive the MBSR compared with participants who do not receive the MBSR treatment. In order to participate, individuals must be: male, living with HIV, age 18-70 years, live within one hour of participating centre, and have a good understanding of the English language. Questionnaires will be completed before individuals begin the program, at the end of the intensive phase (8 weeks) and at 6 months after the start of the group program. The primary program evaluation outcome will be a reduction in stress; secondary evaluation outcomes will include the improvements in the physical and emotional experience of pain as well as general psychosocial functioning and self-esteem.
Detailed Description
In most health care settings, psychosocial interventions that target stress and distress states that are integrated into routine HIV care will need to serve a large number of patients. Due to their time- and cost- efficiency, group approaches are being used increasingly in medical settings to address this need. One approach that has been used successfully in cancer and other chronic diseases is mindfulness-based stress reduction (MBSR), an 8-week manualized treatment program that provides mood management techniques based on training in mindfulness, a metacognitive skill. A recent randomized controlled trial in cancer demonstrated that this brief intervention significantly reduced anxiety and depression symptoms and that these gains were maintained at a six-month follow-up. Similar results have been obtained in a heterogeneous sample of medical patients. Although research in this area is in its infancy, it does appear that MBSR may be effective in the management of anxiety and mood symptoms that are common across various medical conditions and thus may be a good treatment option in men living with HIV. Preliminary evidence, gathered from a pilot assessment of an MBSR program for HIV positive men, demonstrated significant pre- to post-intervention reductions in anxiety and depression, as well as overall mood disturbance scores on standardized measures, and thus, MBSR has promise in this population. A randomized controlled trial is clearly needed however before can be recommended as a psychosocial treatment for men with HIV. It is predicted that MBSR will be effective in mitigating anxiety and depressive symptoms, as well as HIV-related distress, among HIV patients (Hypothesis #1). MBSR appears to be particularly well suited for anxiety- and depression- spectrum symptoms because it targets cognitive processes that contribute to and maintains them. Current cognitive models emphasize the central role of worry and rumination in the onset and maintenance of anxiety and depression, respectively. Worry can perpetuate an upward spiral of increased emotional arousal and intrusive thoughts heightening anxiety symptoms. Similarly, rumination can escalate a spiraling cycle of dysphoric affect and associated negative thinking that can lead eventually to a major depressive episode. (MBSR utilizes training in attention regulation that is thought to provide patients with a skill that enables them to disengage from patterns of worry and rumination that otherwise would perpetuate negative affect. Consistent with this prediction, Dr. Bishop (co-investigator) has found evidence from a recently completed pilot study that mindfulness training results in decreased frequency of worry and rumination. Although preliminary, MBSR may be associated with decreases in both worry and rumination (Hypothesis #2) and that, consistent with current cognitive models, decreases in worry and rumination would moderate the reductions in anxiety and depression, respectively (Hypothesis #3). We are also interested in whether this approach is effective for the management of pain, which is prevalent in this population. There is substantial evidence that anxiety, and particularly pain-related fear, can heighten the perception of the intensity and unpleasantness of pain and that anxiety management can lessen pain. Since we anticipate that MBSR will reduce anxiety in this study, we would further expect that it would also reduce the subjective experience of pain (Hypothesis #4). There is some evidence from an uncontrolled trial suggesting that MBSR may be highly effective for managing chronic pain. If MBSR can be used to effectively mitigate pain, then this too would have a recursive effect on mood. Pain in medical populations is a significant factor in emotional distress and psychiatric morbidity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Mindfulness, HIV, Male, Living with HIV, 18-70 years of age, live within one hour of hospital, fluent in English, Complementary Therapies, HIV Therapeutic Vaccine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
117 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Participants in the first arm participate in an 8-week MBSR group
Arm Title
2
Arm Type
Active Comparator
Arm Description
Participants assigned to the control arm do not receive the MBSR program but may or may not be receiving current psychotherapy or counselling
Intervention Type
Behavioral
Intervention Name(s)
MBSR group
Intervention Description
8-week MBSR group, 3 hours per week plus one all day retreat
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
Treatment as usual, which could include medications or psychotherapy
Primary Outcome Measure Information:
Title
Subjects in the MBSR group will have greater improvement in measures of psychosocial functioning (i.e. anxiety, depression, HIV-related distress, affectivity) at 8 weeks and 6-months post-intervention
Time Frame
8 weeks and 6 months after start of intervention
Title
Subjects in the MBSR group will demonstrate significantly greater improvement on measures of worry and rumination at 8 weeks and 6-months post-intervention
Time Frame
8 weeks and 6 months after start of intervention
Title
MBSR will result in greater improvement in pain compared to the control arm
Time Frame
8 weeks and 6 months after start of intervention
Secondary Outcome Measure Information:
Title
Reductions in anxiety and depression during MBSR will be moderated by reductions in worry and ruminations, respectively
Time Frame
8 weeks and 6 months after start of intervention

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male Living with HIV 18-70 years of age Fluent in English Lives within one hour of the hospital Exclusion Criteria: Severe depression Current suicide ideation Substance abuse Impaired cognitive function
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bill Gayner, M.S.W.
Organizational Affiliation
MOUNT SINAI HOSPITAL
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mary Jane Esplen, Ph.D.
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mount Sinai Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1X5
Country
Canada

12. IPD Sharing Statement

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A Randomized Controlled Trial of a Mindfulness-Based Stress Reduction Intervention for Men Living With HIV

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