TinnitusPhase 2MBTRNCT01229709
Mindfulness Based Tinnitus Reduction (MBTR): A Symptom Perception Shift Program
A Phase 2 study testing Mindfulness Based Tinnitus Reduction in people with Tinnitus and Anxiety, run by University of California, San Francisco at 2 sites in United States.
Trial summary
This study is a randomized, controlled trial of Mindfulness Based Tinnitus Reduction (MBTR) vs. Treatment As Usual (TAU). This study aims to determine patient's benefit from participating in an 8-week MBTR program as measured by a reduction in clinical symptoms, if present, and a tinnitus symptom perception shift. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Tinnitus, Anxiety, Depression
- What is being tested?
- Mindfulness Based Tinnitus Reduction
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 10 participants
- Where
- 2 sitesUnited States
- Study dates
- Jan 2011to Jun 2011
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age > 18
- English speaking
- Duration of subjective chronic tinnitus > 6 months
- Moderate to strong tinnitus annoyance (Minimum THI score of > 28 )
Who cannot join
- Age < 18
- Non-English speaking
- > Moderate Hearing Loss
- Duration of chronic subjective tinnitus < 6 months
- Treatable tinnitus
- Severe depression and/or anxiety
Show all 13Show fewer
- Recent (within 3-month) history of alcohol or drug abuse or dependence other than tobacco or caffeine
- No recent (within 3 months) start of new tinnitus treatment
- THI score < 28
- No previous psychological treatment for their tinnitus.
- History of traumatic brain injury (TBI) with loss of consciousness (LOC)
- History of psychotic disorders or dementia
- Currently undergoing litigation or legal matters related to auditory disorders
Trial locations and contacts
2 sites in 1 country.
United States2 sites
UCSF Audiology Clinic
San Francisco, California, 94115
UCSF
San Francisco, California, 94115
About this study
Official title: Phase 2 Mindfulness Based Tinnitus Reduction (MBTR) Study: A Symptom Perception Shift Program
This study is a randomized, controlled trial of Mindfulness Based Tinnitus Reduction (MBTR) vs. Treatment As Usual (TAU). This study aims to determine patient's benefit from participating in an 8-week MBTR program as measured by a reduction in clinical symptoms, if present, and a tinnitus symptom perception shift. Sixty-four tinnitus patients who have previously received Tinnitus Counseling (TAU) at the UCSF Audiology Clinic under the direction of Robert Sweetow, PhD will be invited to participate in the MBTR study. Subjects will be randomly assigned to the experimental and control groups of 32 each. All subjects will have received Tinnitus Counseling at least 6-months prior to entry into the study. Tinnitus symptom activity and discomfort as well as psychological outcomes will be assessed by self-report questionnaires. The primary outcome measure is the Tinnitus Handicap Inventory (THI) measuring tinnitus symptom severity. The secondary outcome measures include the Tinnitus Visual Analogue Scale (TVAS), the Symptom Checklist-90-Revised (SCL-90-R), Hamilton Anxiety and Depression Scale (HADS), and the Five Factor Mindfulness Questionnaire (FFMQ). In addition to tinnitus symptom severity, secondary outcome measures are used to measure change in mindfulness and other clinical symptoms such as anxiety and depression, if they exist. The experimental group will complete measures at pre-, post-, at 3-months and 12-months follow-up. A 12-month follow-up assessment will be conducted with the experimental group to identify any enduring effects of the treatment. The control group will fill out measures at pre-, post-, and 3-month time periods. The 12-month follow-up will be conducted with the experimental group only and will be the uncontrolled portion of the study.
The purpose of this study is to 1) Design and execute an MBTR program for patients with tinnitus within the UCSF Department of Audiology. 2) Determine patient's benefit from participating in an 8-week MBTR program as measured by a decrease in tinnitus distress, and a reduction in clinical symptoms (i.e., depression, anxiety), if present. 3) Compare the responses on study measures to those of the control group. 4) Collect follow-up data at 6- and 12-months post intervention to assess enduring effects, if any, in the experimental group. 5) Use the data and patient feedback to modify UCSF's Audiology program and guide future programming in regards to the treatment and care of patients with tinnitus.
Read the detailed description
Tinnitus is a medical term for acoustical perceptions heard in the ear(s) or head, not produced by external sound. This sound can be experienced as a ringing, buzzing, whooshing, or hissing. Estimates suggest that as many as 50 million people in the United States experience tinnitus to some degree. Approximately 12 million of these people experience tinnitus bothersome enough to seek medical treatment. Two to 3 million Americans are severely affected by their tinnitus to the extent that their ability to function is severely impaired.
Mindfulness Based Stress Reduction (MBSR) is an established treatment with broad applicability to clinical science. MBSR has been scientifically shown to improve well-being and health in the treatment of depression (Mason O, Hargreaves I. 2001), anxiety (Kabat-Zinn, et al 1992), stress (Kabat-Zinn, et al. 1992), fibromyalgia (Grossman, et al. 2007), chronic fatigue (Surawy, et al. 2005), psoriasis (Kabat-Zinn, et al. 2003), treatment of cancer (Speca, et al. 2006), multiple schlerosis (Grossman, et al. 2010), and pain (Kabat-Zinn, et al. 1985).
Treatments used for pain management are of particular interest to those studying tinnitus because many similarities between individuals suffering with tinnitus and pain can be drawn. Both pain and tinnitus patients commonly express a perceived lack of control over their symptoms, problems with aspects of attention and focus, maladaptive coping strategies, catastrophic thinking, and the use of similar treatment methods (e.g., cognitive coping strategies, CBT, relaxation techniques)(Moller, 2000, Tonndorf, 1987). Like intractable pain, there is no single identifiable cause of tinnitus, there is no single medical or surgical treatment that is effective, there are a wide range of psychological effects, and one's lifestyle and general health are particularly affected. One of the first studies looking at mindfulness as a means of pain management was conducted by Jon Kabat-Zinn, Lipworth, and Burney (1985). They took 90 patients with chronic pain and trained them in a ten-week stress reduction and relaxation program. Significant reductions in present moment pain, negative body image, inhibition of activity by pain, mood disturbance such as anxiety and depression were shown. Significant improvements in activity level and feelings of self-esteem were also reported. Reductions and improvements were maintained 15-months post-treatment. Due to the success of mindfulness-based interventions with chronic pain, the healing benefits of mindfulness are being translated to tinnitus care in this study.
To date only one pilot study has been conducted using mindfulness meditation as a treatment for tinnitus. A study conducted in Wales by Sadlier, Stephens, \& Kennedy (2008) used a combination of cognitive behavioral therapy and mindfulness meditation to treat 25 individuals with chronic tinnitus. The subjects were split into two groups. The treatment group received four one-hour sessions of CBT and Mindfulness Meditation practice while the second group waited 3-months and was then treated with the same intervention. Significant reductions in tinnitus post-treatment and at 4 to 6 months follow-up were recorded. The proposed MBTR study isolates mindfulness from CBT approaches to tinnitus, and may be an important contribution to the clinical literature on the care of tinnitus.
Introduction and Specific Aims This study aims to determine the efficacy of MBTR in reducing symptoms of tinnitus in adults. Primary objectives include: 1) Design and execute an MBTR program within the UCSF Department of Audiology for patients with tinnitus. 2) Determine patient's benefit from participating in an 8-week MBTR program as measured by a reduction in clinical symptoms, if present, and a tinnitus symptom perception shift. 3) Compare the responses on study measures to those of the control group. 4) Use the data and patient feedback to modify UCSF's Audiology program and guide future programming in regards to the treatment and care of patients with tinnitus.
The above mentioned objectives will be met through testing the following primary hypotheses:
Hypothesis 1a: MBTR + TAU will be more effective than TAU alone in reducing tinnitus symptoms (25-item Tinnitus Handicap Inventory [THI]) in adult patients with chronic tinnitus over an 8-week period.
Hypothesis 1b: MBTR + TAU will be more effective than TAU alone in reducing tinnitus symptoms (25-item Tinnitus Handicap Inventory [THI]) in adult patients with chronic tinnitus at 3-months follow-up.
Hypothesis 1c: Reduction in tinnitus symptoms (25-item Tinnitus Handicap Inventory [THI]) in the MBTR + TAU will be maintained at 12-months follow-up.
Secondary hypotheses and analyses are as follows:
Hypothesis 2: Effect on Functional Status: MBTR + TAU will be more effective than TAU alone in reducing anxiety and depressive symptoms, if they exist (17-item Hamilton Anxiety and Depression Scale [HADS]) and in reducing additional clinical symptoms, if they exist (90-item Symptom Checklist-90-Revised [SCL-90-R]) and enhanced mindfulness (39-item Five Factor Mindfulness Questionnaire [FFMQ]).
Hypothesis 3: Mediators of MBTR Efficacy: The effect of MBTR on tinnitus severity (THI, Tinnitus Visual Analogue Scale [TVAS]) and functional status (HADS and SCL-90-R) will be mediated by enhanced mindfulness (FFMQ).
Hypothesis 4: Length of Efficacy: We will assess whether treatment gains in tinnitus severity (THI, TVAS), functional status (HADS, SCL-90-R), and mindfulness (FFMQ) are retained at 3-months and at 12-months follow-up for the experimental group.
Research Design and Methods Subject Recruitment A chart review of past patients (approximately 700) from the UCSF Audiology Clinic who have been seen for Tinnitus Counseling (Treatment as Usual-TAU) at least six-months prior to enrollment in the study will take place. A list of the inclusion/exclusion criteria are below.
Inclusion Criteria
Subject Characteristics
- Age > 18
- English speaking
- Duration of subjective chronic tinnitus > 6 months
- Received Tinnitus Counseling (TAU) at the UCSF Audiology Clinic > 6 months prior to entering the study
- Moderate to strong tinnitus annoyance (Minimum THI score of > 24 per chart review)
Exclusion Criteria
Subject Characteristics
- Age < 18
- Non-English speaking
- > Moderate Hearing Loss
- Duration of chronic subjective tinnitus < 6 months
- Severe depression and/or anxiety (as measured by the HADS)
- Recent (within 3-month) history of alcohol or drug abuse or dependence other than tobacco or caffeine
- No recent (within 3 months) start of new tinnitus treatment
- History of psychotic disorders or dementia
- THI score < 24
- Currently undergoing litigation or legal matters related to auditory disorders
Three hundred letters will be mailed to those patients from the Clinic's database who meet inclusion criteria and have been seen for tinnitus counseling at least six-months prior to entry into the study. Patients will respond via postcard as to whether they would like to learn more about the study. Patients will be informed in the letter that if no response is received via postcard to the Clinic within two weeks, a research assistant will follow up with a phone call as a reminder to respond. To prevent over-enrollment/recruitment of subjects, letters will be sent out in waves of 100 at a time. Recruitment will stop when 80 patients respond to participate (a 20% drop out-rate is expected bringing the number down to 64).
The 80 patients who express interest in participating in the study and meet inclusion criteria per chart review will be invited to take part in a 30-minute individual interview with one of the two MBTR course instructors prior to beginning the program. The 30-minute individual interview will serve as an orientation to the MBTR program at which time consents will be signed. Subjects will be randomly assigned to 2 groups of 32 participants, and at the completion of the 30-minute interview a research assistant will administer baseline psychometric assessments (see below for the list of measures used).
Primary Outcome Measures
- Tinnitus Handicap Inventory (THI) The THI is a self-report measure that can be used in a busy clinical practice to quantify the impact of tinnitus on daily living. The measure is brief, easy to administer and interpret, broad in scope, and psychometrically robust. Convergent validity was assessed using another measure of perceived tinnitus handicap (Tinnitus Handicap Questionnaire). Construct validity was assessed using the Beck Depression Inventory, Modified Somatic Perception Questionnaire, symptom rating scales (annoyance, sleep disruption, depression, and concentration), and perceived tinnitus pitch and loudness judgments. The THI is comprised of 25-item items grouped into functional, emotional, and catastrophic subscales. The total scales yield excellent internal consistency reliability (Cronbach's alpha=.93).
Secondary Outcome Measures
- Tinnitus Visual Analogue Scale (TVAS) Tinnitus Visual Analogue Scale (VAS) is a collection of straight lines 100mm in length anchored at the end with extremes (e.g., not bothersome, extremely bothersome) of the tinnitus sensation, feeling or response. The strength of this method lies in the compellation of several measurements (e.g., weekly average of tinnitus annoyance). This method of measuring distress has been recommended for use in research (Axelsson, Coles, Erlandsson, Meikle, \& Vernon, 1993).
- Hospital Anxiety and Depression Scale (HADS) The HADS (Zigmond \& Snaith, 1983) was chosen as a measure of self-reported depression and anxiety. As compared to the Beck Depression Inventory and State Trait Anxiety Inventory, the HADS is a 14 item questionnaire and does not tend to overburden or exhaust patients regarding filling out measures. The HADS is a more discrete measure that controls for complaints better explained by the somatic problem than does the BDI or STAI (Hermann, 1997).
- The Symptom Checklist-90-Revised (SCL-90-R) The Symptom Checklist-90-Revised (SCL-90-R) will be used to assess psychological distress (Derogatis 1983). SCL-90-R is a 90-item questionnaire measuring psychological distress over the past week. Reliability and validity of the measure is found to be high. The Global Severity Index (GSI) is used as a measure of overall psychological distress. The SCL-90-R has been used in several previous MBSR studies to measure psychological status (Kabat-Zinn, et al. 1992; Kabat-Zinn, et al. 1985; Kabat-Zinn, et al.1987; Kaplan, et al. 1993; Miller, et al. 1995; Majumdar, et al. 2002).
- Five Facet Mindfulness Questionnaire (FFMQ) Five-Facet Mindfulness Questionnaire (FFMQ; R. A. Baer, Smith, Hopkins, Krietemeyer, \& Toney, 2006), is a 39-item inventory assessing five facets of mindfulness.
The FFMQ has been shown to have strong psychometric characteristics, including adequate to good internal consistencies for all facets and significant correlations in predicted directions with a variety of other constructs (R. A. Baer et al., 2006, 2008).
Description of MBTR Course The Mindfulness Based Tinnitus Reduction (MBTR) program is an 8-week course held one evening per week for 2 ½ hours. Participants will also complete a day-long Sunday retreat between the 6th and 7th sessions.
Modeled after the original Mindfulness Based Stress Reduction (MBSR) program developed by Jon Kabat-Zinn, PhD at the University of Massachusetts Medical Center, the MBTR course will introduce participants to mindfulness practice in the form of sitting meditation, body awareness and mindful movement, and informal mindfulness practices of daily life (e.g., eating, communicating, working, coping). Meditation will be introduced in four formats: sitting meditation using the breath as an anchor of attention, sitting meditation characterized by a state of open awareness, progressive body relaxation, and contemplative walking. Participants will be asked to practice at home for 30 minutes 6 days per week between sessions, aided by an audio CD. The two MBSR trained co-investigators will co-lead the classes. Participants will be provided with a copy of Full Catastrophe Living by Jon Kabat-Zinn, PhD. Intervention participants will be asked to document the number of minutes spent daily on each practice at home during their participation in the 8-week program.
MBTR Course Outline
The course in Mindfulness-Based Tinnitus Reduction (MBTR) takes place over eight weeks. Classes are approximately 2-1/2 hours long and are held in the evening once a week. Each class consists of guided meditations, gentle movement exercises, lecture, and group discussion as mindfulness relates to their experience with tinnitus. The course includes an all-day session on a Sunday between the sixth and seventh week. Between classes, subjects will enhance their participation through working with meditation CDs, homework assignments, and readings from the course materials and textbook. The in-class curriculum includes the following components:
- Week 1: Introduction to Program ° Foundations of Mindfulness ° More right with you than wrong ° Introduction to Body Scan meditation ° Tinnitus Discussion
- Week 2: Patience ° Working with perceptions °The Wandering Mind ° The STOP exercise
- Week 3: Non-Striving ° Introduction to Awareness of Breathing Meditation ° Mindful Yoga
- ° Attention vs. Disattention ° Tinnitus Discussion
- Week 4: Non-Judging ° Responding vs. Reacting ° Seeing Our Patterns ° Sitting Meditation
- ° Standing Yoga ° Research on Stress \& Stress Hardiness ° Tinnitus Discussion
- Week 5: Acknowledgment ° Group Reflections on Halfway Point ° Small \& Large Groups ° Sitting Meditation ° Qi Gong ° Tinnitus Discussion
- Week 6: Letting it Be ° Skillful Communication ° Avoiding Difficulty vs. Entering and Blending° Loving-kindness Meditation ° Walking Meditation ° Tinnitus Discussion
Daylong Session (see outline below)
- Week 7: Sitting Meditation ° Mindful Movement ° Trust \& Self-Reliance ° Learning How to Practice on One's Own ° Mindfulness in Everyday Life ° Tinnitus Discussion
- Week 8: Sitting Meditation ° Mindful Movement ° The Class Never Ends: Practice for the rest of Your Life ° Course Review \& Group Reflection
Mindfulness-Based Tinnitus Reduction Daylong Outline
The Mindfulness-Based Tinnitus Reduction Daylong (9:30am to 4:30pm between the 6th and 7th weeks) is part of the course and consists of a day of lead meditations, gentle movement exercises, and group sharing. A typical schedule is as follows:
9:30: Introductions 10:00: Awareness of Breathing 10:15: Yoga 10:30: Body Scan Meditation 11:15: Walking Meditation 11:45: Sitting Meditation 12:15: Lunch \& Rest 1:30: Yoga 2:00: Sitting Meditation 2:30: Walking Meditation 2:45: Sitting Meditation 3:10: Walking Meditation 3:25: Lovingkindness Meditation 3:45: Group Discussion (Check Out) 4:30: Farewell
- Conditions
- Tinnitus, Anxiety, Depression
- Being tested
- Mindfulness Based Tinnitus Reduction
- Keywords
- Tinnitus, Mindfulness, MBSR, Mindfulness Based Stress Reduction, MBTR
- Medical subject headings
- Tinnitus, Anxiety Disorders, Depression
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Mindfulness Based Tinnitus ReductionBehavioural
Also called MBTR
The Mindfulness Based Tinnitus Reduction (MBTR) program will be held for two-and-a-half hours one evening per week over 8 consecutive weeks. Participants will also complete a day-long Sunday retreat between the 6th and 7th sessions. Each participant will take part in a 30-minute private interview with the course instructor prior to beginning the program.
| Study group | Role | What they receive |
|---|---|---|
| Mindfulness Based Tinnitus Reduction | Experimental | Not described Receives: Behavioral: Mindfulness Based Tinnitus Reduction |
| Tinnitus Counseling Only Control | No intervention | Control group subjects will have had treatment as usual (TAU) care from the UCSF Audiology Clinic which includes Tinnitus Counseling (TC) at least three-months prior to enty into the study. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Tinnitus Handicap Inventory (THI)
The THI is a self-report measure that can be used in a busy clinical practice to quantify the impact of tinnitus on daily living. The measure is brief, easy to administer and interpret, broad in scope, and psychometrically robust. Convergent validity was assessed using another measure of perceived tinnitus handicap (Tinnitus Handicap Questionnaire). Construct validity was assessed using the Beck Depression Inventory, Modified Somatic Perception Questionnaire, symptom rating scales (annoyance, sleep disruption, depression, and concentration), and perceived tinnitus pitch and loudness judgments. Pre-assessment measures were individually administered to participants at the UCSF Audiology Clinic immediately after consents were signed, no earlier than 2 weeks prior to the start of the intervention. Post-assessment measures were filled out at home and mailed back to the Clinic by participants no more than 2 weeks after the intervention's completion.
Measured: Baseline, Post-intervention (within 2 weeks after completion of 8-week intervention)
Secondary outcomes (4)
Change in Symptom Checklist-90- Revised
Pre-assessment measures were individually administered to participants at the UCSF Audiology Clinic immediately after consents were signed, no earlier than 2 weeks prior to the start of the intervention. Post-assessment measures were filled out at home and mailed back to the Clinic by participants no more than 2 weeks after the intervention's completion.
Measured: Baseline, Post-intervention (within 2 weeks after completion of 8-week intervention)
Change in Five-Factor Mindfulness Questionnaire (FFMQ)
Pre-assessment measures were individually administered to participants at the UCSF Audiology Clinic immediately after consents were signed, no earlier than 2 weeks prior to the start of the intervention. Post-assessment measures were filled out at home and mailed back to the Clinic by participants no more than 2 weeks after the intervention's completion.
Measured: Baseline, Post-intervention (within 2 weeks after completion of 8-week intervention)
Change in Hamilton Anxiety & Depression Scale (HADS)
Pre-assessment measures were individually administered to participants at the UCSF Audiology Clinic immediately after consents were signed, no earlier than 2 weeks prior to the start of the intervention. Post-assessment measures were filled out at home and mailed back to the Clinic by participants no more than 2 weeks after the intervention's completion.
Measured: Baseline, Post-intervention (within 2 weeks after completion of 8-week intervention)
Change in Tinnitus Visual Analogue Scale (VAS)
Tinnitus Visual Analogue Scale (VAS) is a collection of straight lines 100mm in length anchored at the end with extremes (e.g., no tinnitus distress, extreme tinnitus distress) of the tinnitus sensation, feeling or response. This means of measuring distress has been suggested for use in research (Axelsson, Coles, Erlandsson, Meikle, \& Vernon, 1993). Pre-assessment measures were individually administered to participants at the UCSF Audiology Clinic immediately after consents were signed, no earlier than 2 weeks prior to the start of the intervention. Post-assessment measures were filled out at home and mailed back to the Clinic by participants no more than 2 weeks after the intervention's completion.
Measured: Baseline, Post-intervention (within 2 weeks after completion of 8 week intervention)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Oct 2010 (estimated)
- Study startJan 2011
- Primary completionJun 2011
- Study completionJun 2011
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (15)Papers the sponsor has linked to this study.
- Other trials for TinnitusStudies of the same condition, open and under way.
- More trials run by University of California, San FranciscoThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 10 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of California, San Francisco
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Jennifer Gans, PsyD, Study director, Clinical Psychologist
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01229709
- Sponsor's protocol ID
- H8935-35834-01
- Acronym
- MBTR
- Status last verified
- Oct 2014
- First submitted
- 26 Oct 2010
- Last updated
- 28 Oct 2014
- Results posted
- No
- Data monitoring committee
- Yes
Publications
Andersson G. Psychological aspects of tinnitus and the application of cognitive-behavioral therapy. Clin Psychol Rev. 2002 Sep;22(7):977-90. doi: 10.1016/s0272-7358(01)00124-6.
PubMed 12238249Grossman P, Tiefenthaler-Gilmer U, Raysz A, Kesper U. Mindfulness training as an intervention for fibromyalgia: evidence of postintervention and 3-year follow-up benefits in well-being. Psychother Psychosom. 2007;76(4):226-33. doi: 10.1159/000101501.
PubMed 17570961Henry, J. L., & Wilson, P. H. (2001). The psychological management of chronic tinnitus. Needham Heights, MA: Allyn & Bacon.
Kabat-Zinn J, Massion AO, Kristeller J, Peterson LG, Fletcher KE, Pbert L, Lenderking WR, Santorelli SF. Effectiveness of a meditation-based stress reduction program in the treatment of anxiety disorders. Am J Psychiatry. 1992 Jul;149(7):936-43. doi: 10.1176/ajp.149.7.936.
PubMed 1609875Kabat-Zinn J, Lipworth L, Burney R. The clinical use of mindfulness meditation for the self-regulation of chronic pain. J Behav Med. 1985 Jun;8(2):163-90. doi: 10.1007/BF00845519.
PubMed 3897551Kabat-Zinn J, Wheeler E, Light T, Skillings A, Scharf MJ, Cropley TG, Hosmer D, Bernhard JD. Influence of a mindfulness meditation-based stress reduction intervention on rates of skin clearing in patients with moderate to severe psoriasis undergoing phototherapy (UVB) and photochemotherapy (PUVA). Psychosom Med. 1998 Sep-Oct;60(5):625-32. doi: 10.1097/00006842-199809000-00020.
PubMed 9773769Mason O, Hargreaves I. A qualitative study of mindfulness-based cognitive therapy for depression. Br J Med Psychol. 2001 Jun;74 Part 2:197-212.
PubMed 11802836Moller AR. Similarities between severe tinnitus and chronic pain. J Am Acad Audiol. 2000 Mar;11(3):115-24.
PubMed 10755808Pradhan EK, Baumgarten M, Langenberg P, Handwerger B, Gilpin AK, Magyari T, Hochberg MC, Berman BM. Effect of Mindfulness-Based Stress Reduction in rheumatoid arthritis patients. Arthritis Rheum. 2007 Oct 15;57(7):1134-42. doi: 10.1002/art.23010.
PubMed 17907231Sadlier M, Stephens SD, Kennedy V. Tinnitus rehabilitation: a mindfulness meditation cognitive behavioural therapy approach. J Laryngol Otol. 2008 Jan;122(1):31-7. doi: 10.1017/S0022215107007438. Epub 2007 Apr 23.
PubMed 17451612Speca, M., Carlson, L. E., Mackenzie, M. J., & Angen, M. (2006). Mindfulness-based stress reduction (MBSR) as an intervention for cancer patients. In R. A. Baer (Ed.), Mindfulness-based treatment approaches: Clinician's guide to evidence base and applications (pp. 239-261). San Diego, CA: Elsevier Academic Press.
Surawy C, Roberts J, Silver A. (2005). The effect of mindfulness training on mood and measures of fatigue, activity, and quality of life in patients with chronic fatigue syndrome on a hospital waiting list: a series of exploratory studies. Behavioural and Cognitive Psychotherapy; 33:103-09
Sweetow RW. Cognitive aspects of tinnitus patient management. Ear Hear. 1986 Dec;7(6):390-6. doi: 10.1097/00003446-198612000-00008.
PubMed 3792682Tonndorf J. The analogy between tinnitus and pain: a suggestion for a physiological basis of chronic tinnitus. Hear Res. 1987;28(2-3):271-5. doi: 10.1016/0378-5955(87)90054-2.
PubMed 2820913Williams, M., Teasdale, J., Zindel, S., Kabbat-Zinn, J.. (2007). The mindful way through depression. NY: The Guilford Press.
Study at a glance
From the registry record, last updated by the sponsor on 28 Oct 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Phase 2 Mindfulness Based Tinnitus Reduction (MBTR) Study: A Symptom Perception Shift Program
- ClinicalTrials.gov ID
- NCT01229709
- Acronym / sponsor ID
- MBTR / H8935-35834-01
- Conditions
- Tinnitus, Anxiety, Depression
- Keywords
- Tinnitus, Mindfulness, MBSR, Mindfulness Based Stress Reduction, MBTR
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 10 participants (actual)
- Lead sponsor
- University of California, San FranciscoUniversity, hospital or other
- Study start
- Jan 2011
- Primary completion
- Jun 2011 (actual)
- Study completion
- Jun 2011 (actual)
- First posted
- 28 Oct 2010 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study is a randomized, controlled trial of Mindfulness Based Tinnitus Reduction (MBTR) vs. Treatment As Usual (TAU). This study aims to determine patient's benefit from participating in an 8-week MBTR program as measured by a reduction in clinical symptoms, if present, and a tinnitus symptom perception shift. Sixty-four tinnitus patients who have previously received Tinnitus Counseling (TAU) at the UCSF Audiology Clinic under the direction of Robert Sweetow, PhD will be invited to participate in the MBTR study. Subjects will be randomly assigned to the experimental and control groups of 32 each. All subjects will have received Tinnitus Counseling at least 6-months prior to entry into the study. Tinnitus symptom activity and discomfort as well as psychological outcomes will be assessed by self-report questionnaires. The primary outcome measure is the Tinnitus Handicap Inventory (THI) measuring tinnitus symptom severity. The secondary outcome measures include the Tinnitus Visual Analogue Scale (TVAS), the Symptom Checklist-90-Revised (SCL-90-R), Hamilton Anxiety and Depression Scale (HADS), and the Five Factor Mindfulness Questionnaire (FFMQ). In addition to tinnitus symptom severity, secondary outcome measures are used to measure change in mindfulness and other clinical symptoms such as anxiety and depression, if they exist. The experimental group will complete measures at pre-, post-, at 3-months and 12-months follow-up. A 12-month follow-up assessment will be conducted with the experimental group to identify any enduring effects of the treatment. The control group will fill out measures at pre-, post-, and 3-month time periods. The 12-month follow-up will be conducted with the experimental group only and will be the uncontrolled portion of the study.
The purpose of this study is to 1) Design and execute an MBTR program for patients with tinnitus within the UCSF Department of Audiology. 2) Determine patient's benefit from participating in an 8-week MBTR program as measured by a decrease in tinnitus distress, and a reduction in clinical symptoms (i.e., depression, anxiety), if present. 3) Compare the responses on study measures to those of the control group. 4) Collect follow-up data at 6- and 12-months post intervention to assess enduring effects, if any, in the experimental group. 5) Use the data and patient feedback to modify UCSF's Audiology program and guide future programming in regards to the treatment and care of patients with tinnitus.
Detailed description
Tinnitus is a medical term for acoustical perceptions heard in the ear(s) or head, not produced by external sound. This sound can be experienced as a ringing, buzzing, whooshing, or hissing. Estimates suggest that as many as 50 million people in the United States experience tinnitus to some degree. Approximately 12 million of these people experience tinnitus bothersome enough to seek medical treatment. Two to 3 million Americans are severely affected by their tinnitus to the extent that their ability to function is severely impaired.
Mindfulness Based Stress Reduction (MBSR) is an established treatment with broad applicability to clinical science. MBSR has been scientifically shown to improve well-being and health in the treatment of depression (Mason O, Hargreaves I. 2001), anxiety (Kabat-Zinn, et al 1992), stress (Kabat-Zinn, et al. 1992), fibromyalgia (Grossman, et al. 2007), chronic fatigue (Surawy, et al. 2005), psoriasis (Kabat-Zinn, et al. 2003), treatment of cancer (Speca, et al. 2006), multiple schlerosis (Grossman, et al. 2010), and pain (Kabat-Zinn, et al. 1985).
Treatments used for pain management are of particular interest to those studying tinnitus because many similarities between individuals suffering with tinnitus and pain can be drawn. Both pain and tinnitus patients commonly express a perceived lack of control over their symptoms, problems with aspects of attention and focus, maladaptive coping strategies, catastrophic thinking, and the use of similar treatment methods (e.g., cognitive coping strategies, CBT, relaxation techniques)(Moller, 2000, Tonndorf, 1987). Like intractable pain, there is no single identifiable cause of tinnitus, there is no single medical or surgical treatment that is effective, there are a wide range of psychological effects, and one's lifestyle and general health are particularly affected. One of the first studies looking at mindfulness as a means of pain management was conducted by Jon Kabat-Zinn, Lipworth, and Burney (1985). They took 90 patients with chronic pain and trained them in a ten-week stress reduction and relaxation program. Significant reductions in present moment pain, negative body image, inhibition of activity by pain, mood disturbance such as anxiety and depression were shown. Significant improvements in activity level and feelings of self-esteem were also reported. Reductions and improvements were maintained 15-months post-treatment. Due to the success of mindfulness-based interventions with chronic pain, the healing benefits of mindfulness are being translated to tinnitus care in this study.
To date only one pilot study has been conducted using mindfulness meditation as a treatment for tinnitus. A study conducted in Wales by Sadlier, Stephens, \& Kennedy (2008) used a combination of cognitive behavioral therapy and mindfulness meditation to treat 25 individuals with chronic tinnitus. The subjects were split into two groups. The treatment group received four one-hour sessions of CBT and Mindfulness Meditation practice while the second group waited 3-months and was then treated with the same intervention. Significant reductions in tinnitus post-treatment and at 4 to 6 months follow-up were recorded. The proposed MBTR study isolates mindfulness from CBT approaches to tinnitus, and may be an important contribution to the clinical literature on the care of tinnitus.
Introduction and Specific Aims This study aims to determine the efficacy of MBTR in reducing symptoms of tinnitus in adults. Primary objectives include: 1) Design and execute an MBTR program within the UCSF Department of Audiology for patients with tinnitus. 2) Determine patient's benefit from participating in an 8-week MBTR program as measured by a reduction in clinical symptoms, if present, and a tinnitus symptom perception shift. 3) Compare the responses on study measures to those of the control group. 4) Use the data and patient feedback to modify UCSF's Audiology program and guide future programming in regards to the treatment and care of patients with tinnitus.
The above mentioned objectives will be met through testing the following primary hypotheses:
Hypothesis 1a: MBTR + TAU will be more effective than TAU alone in reducing tinnitus symptoms (25-item Tinnitus Handicap Inventory [THI]) in adult patients with chronic tinnitus over an 8-week period.
Hypothesis 1b: MBTR + TAU will be more effective than TAU alone in reducing tinnitus symptoms (25-item Tinnitus Handicap Inventory [THI]) in adult patients with chronic tinnitus at 3-months follow-up.
Hypothesis 1c: Reduction in tinnitus symptoms (25-item Tinnitus Handicap Inventory [THI]) in the MBTR + TAU will be maintained at 12-months follow-up.
Secondary hypotheses and analyses are as follows:
Hypothesis 2: Effect on Functional Status: MBTR + TAU will be more effective than TAU alone in reducing anxiety and depressive symptoms, if they exist (17-item Hamilton Anxiety and Depression Scale [HADS]) and in reducing additional clinical symptoms, if they exist (90-item Symptom Checklist-90-Revised [SCL-90-R]) and enhanced mindfulness (39-item Five Factor Mindfulness Questionnaire [FFMQ]).
Hypothesis 3: Mediators of MBTR Efficacy: The effect of MBTR on tinnitus severity (THI, Tinnitus Visual Analogue Scale [TVAS]) and functional status (HADS and SCL-90-R) will be mediated by enhanced mindfulness (FFMQ).
Hypothesis 4: Length of Efficacy: We will assess whether treatment gains in tinnitus severity (THI, TVAS), functional status (HADS, SCL-90-R), and mindfulness (FFMQ) are retained at 3-months and at 12-months follow-up for the experimental group.
Research Design and Methods Subject Recruitment A chart review of past patients (approximately 700) from the UCSF Audiology Clinic who have been seen for Tinnitus Counseling (Treatment as Usual-TAU) at least six-months prior to enrollment in the study will take place. A list of the inclusion/exclusion criteria are below.
Inclusion Criteria
Subject Characteristics
- Age > 18
- English speaking
- Duration of subjective chronic tinnitus > 6 months
- Received Tinnitus Counseling (TAU) at the UCSF Audiology Clinic > 6 months prior to entering the study
- Moderate to strong tinnitus annoyance (Minimum THI score of > 24 per chart review)
Exclusion Criteria
Subject Characteristics
- Age < 18
- Non-English speaking
- > Moderate Hearing Loss
- Duration of chronic subjective tinnitus < 6 months
- Severe depression and/or anxiety (as measured by the HADS)
- Recent (within 3-month) history of alcohol or drug abuse or dependence other than tobacco or caffeine
- No recent (within 3 months) start of new tinnitus treatment
- History of psychotic disorders or dementia
- THI score < 24
- Currently undergoing litigation or legal matters related to auditory disorders
Three hundred letters will be mailed to those patients from the Clinic's database who meet inclusion criteria and have been seen for tinnitus counseling at least six-months prior to entry into the study. Patients will respond via postcard as to whether they would like to learn more about the study. Patients will be informed in the letter that if no response is received via postcard to the Clinic within two weeks, a research assistant will follow up with a phone call as a reminder to respond. To prevent over-enrollment/recruitment of subjects, letters will be sent out in waves of 100 at a time. Recruitment will stop when 80 patients respond to participate (a 20% drop out-rate is expected bringing the number down to 64).
The 80 patients who express interest in participating in the study and meet inclusion criteria per chart review will be invited to take part in a 30-minute individual interview with one of the two MBTR course instructors prior to beginning the program. The 30-minute individual interview will serve as an orientation to the MBTR program at which time consents will be signed. Subjects will be randomly assigned to 2 groups of 32 participants, and at the completion of the 30-minute interview a research assistant will administer baseline psychometric assessments (see below for the list of measures used).
Primary Outcome Measures
- Tinnitus Handicap Inventory (THI) The THI is a self-report measure that can be used in a busy clinical practice to quantify the impact of tinnitus on daily living. The measure is brief, easy to administer and interpret, broad in scope, and psychometrically robust. Convergent validity was assessed using another measure of perceived tinnitus handicap (Tinnitus Handicap Questionnaire). Construct validity was assessed using the Beck Depression Inventory, Modified Somatic Perception Questionnaire, symptom rating scales (annoyance, sleep disruption, depression, and concentration), and perceived tinnitus pitch and loudness judgments. The THI is comprised of 25-item items grouped into functional, emotional, and catastrophic subscales. The total scales yield excellent internal consistency reliability (Cronbach's alpha=.93).
Secondary Outcome Measures
- Tinnitus Visual Analogue Scale (TVAS) Tinnitus Visual Analogue Scale (VAS) is a collection of straight lines 100mm in length anchored at the end with extremes (e.g., not bothersome, extremely bothersome) of the tinnitus sensation, feeling or response. The strength of this method lies in the compellation of several measurements (e.g., weekly average of tinnitus annoyance). This method of measuring distress has been recommended for use in research (Axelsson, Coles, Erlandsson, Meikle, \& Vernon, 1993).
- Hospital Anxiety and Depression Scale (HADS) The HADS (Zigmond \& Snaith, 1983) was chosen as a measure of self-reported depression and anxiety. As compared to the Beck Depression Inventory and State Trait Anxiety Inventory, the HADS is a 14 item questionnaire and does not tend to overburden or exhaust patients regarding filling out measures. The HADS is a more discrete measure that controls for complaints better explained by the somatic problem than does the BDI or STAI (Hermann, 1997).
- The Symptom Checklist-90-Revised (SCL-90-R) The Symptom Checklist-90-Revised (SCL-90-R) will be used to assess psychological distress (Derogatis 1983). SCL-90-R is a 90-item questionnaire measuring psychological distress over the past week. Reliability and validity of the measure is found to be high. The Global Severity Index (GSI) is used as a measure of overall psychological distress. The SCL-90-R has been used in several previous MBSR studies to measure psychological status (Kabat-Zinn, et al. 1992; Kabat-Zinn, et al. 1985; Kabat-Zinn, et al.1987; Kaplan, et al. 1993; Miller, et al. 1995; Majumdar, et al. 2002).
- Five Facet Mindfulness Questionnaire (FFMQ) Five-Facet Mindfulness Questionnaire (FFMQ; R. A. Baer, Smith, Hopkins, Krietemeyer, \& Toney, 2006), is a 39-item inventory assessing five facets of mindfulness.
The FFMQ has been shown to have strong psychometric characteristics, including adequate to good internal consistencies for all facets and significant correlations in predicted directions with a variety of other constructs (R. A. Baer et al., 2006, 2008).
Description of MBTR Course The Mindfulness Based Tinnitus Reduction (MBTR) program is an 8-week course held one evening per week for 2 ½ hours. Participants will also complete a day-long Sunday retreat between the 6th and 7th sessions.
Modeled after the original Mindfulness Based Stress Reduction (MBSR) program developed by Jon Kabat-Zinn, PhD at the University of Massachusetts Medical Center, the MBTR course will introduce participants to mindfulness practice in the form of sitting meditation, body awareness and mindful movement, and informal mindfulness practices of daily life (e.g., eating, communicating, working, coping). Meditation will be introduced in four formats: sitting meditation using the breath as an anchor of attention, sitting meditation characterized by a state of open awareness, progressive body relaxation, and contemplative walking. Participants will be asked to practice at home for 30 minutes 6 days per week between sessions, aided by an audio CD. The two MBSR trained co-investigators will co-lead the classes. Participants will be provided with a copy of Full Catastrophe Living by Jon Kabat-Zinn, PhD. Intervention participants will be asked to document the number of minutes spent daily on each practice at home during their participation in the 8-week program.
MBTR Course Outline
The course in Mindfulness-Based Tinnitus Reduction (MBTR) takes place over eight weeks. Classes are approximately 2-1/2 hours long and are held in the evening once a week. Each class consists of guided meditations, gentle movement exercises, lecture, and group discussion as mindfulness relates to their experience with tinnitus. The course includes an all-day session on a Sunday between the sixth and seventh week. Between classes, subjects will enhance their participation through working with meditation CDs, homework assignments, and readings from the course materials and textbook. The in-class curriculum includes the following components:
- Week 1: Introduction to Program ° Foundations of Mindfulness ° More right with you than wrong ° Introduction to Body Scan meditation ° Tinnitus Discussion
- Week 2: Patience ° Working with perceptions °The Wandering Mind ° The STOP exercise
- Week 3: Non-Striving ° Introduction to Awareness of Breathing Meditation ° Mindful Yoga
- ° Attention vs. Disattention ° Tinnitus Discussion
- Week 4: Non-Judging ° Responding vs. Reacting ° Seeing Our Patterns ° Sitting Meditation
- ° Standing Yoga ° Research on Stress \& Stress Hardiness ° Tinnitus Discussion
- Week 5: Acknowledgment ° Group Reflections on Halfway Point ° Small \& Large Groups ° Sitting Meditation ° Qi Gong ° Tinnitus Discussion
- Week 6: Letting it Be ° Skillful Communication ° Avoiding Difficulty vs. Entering and Blending° Loving-kindness Meditation ° Walking Meditation ° Tinnitus Discussion
Daylong Session (see outline below)
- Week 7: Sitting Meditation ° Mindful Movement ° Trust \& Self-Reliance ° Learning How to Practice on One's Own ° Mindfulness in Everyday Life ° Tinnitus Discussion
- Week 8: Sitting Meditation ° Mindful Movement ° The Class Never Ends: Practice for the rest of Your Life ° Course Review \& Group Reflection
Mindfulness-Based Tinnitus Reduction Daylong Outline
The Mindfulness-Based Tinnitus Reduction Daylong (9:30am to 4:30pm between the 6th and 7th weeks) is part of the course and consists of a day of lead meditations, gentle movement exercises, and group sharing. A typical schedule is as follows:
9:30: Introductions 10:00: Awareness of Breathing 10:15: Yoga 10:30: Body Scan Meditation 11:15: Walking Meditation 11:45: Sitting Meditation 12:15: Lunch \& Rest 1:30: Yoga 2:00: Sitting Meditation 2:30: Walking Meditation 2:45: Sitting Meditation 3:10: Walking Meditation 3:25: Lovingkindness Meditation 3:45: Group Discussion (Check Out) 4:30: Farewell
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Mindfulness Based Tinnitus Reduction | Experimental | Behavioral: Mindfulness Based Tinnitus Reduction |
| Tinnitus Counseling Only Control | No intervention | –Control group subjects will have had treatment as usual (TAU) care from the UCSF Audiology Clinic which includes Tinnitus Counseling (TC) at least three-months prior to enty into the study. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Age > 18
- English speaking
- Duration of subjective chronic tinnitus > 6 months
- Moderate to strong tinnitus annoyance (Minimum THI score of > 28 )
Key exclusion criteria (13 listed)
- Age < 18
- Non-English speaking
- > Moderate Hearing Loss
- Duration of chronic subjective tinnitus < 6 months
- Treatable tinnitus
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Mindfulness Based Tinnitus ReductionAlso: MBTRThe Mindfulness Based Tinnitus Reduction (MBTR) program will be held for two-and-a-half hours one evening per week over 8 consecutive weeks. Participants will also complete a day-long Sunday retreat between the 6th and 7th sessions. Each participant will take part in a 30-minute private interview with the course instructor prior to beginning the program. | Behavioural | Mindfulness Based Tinnitus Reduction |
Primary outcome
Change in Tinnitus Handicap Inventory (THI)
Time frame: Baseline, Post-intervention (within 2 weeks after completion of 8-week intervention)
The THI is a self-report measure that can be used in a busy clinical practice to quantify the impact of tinnitus on daily living. The measure is brief, easy to administer and interpret, broad in scope, and psychometrically robust. Convergent validity was assessed using another measure of perceived tinnitus handicap (Tinnitus Handicap Questionnaire). Construct validity was assessed using the Beck Depression Inventory, Modified Somatic Perception Questionnaire, symptom rating scales (annoyance, sleep disruption, depression, and concentration), and perceived tinnitus pitch and loudness judgments. Pre-assessment measures were individually administered to participants at the UCSF Audiology Clinic immediately after consents were signed, no earlier than 2 weeks prior to the start of the intervention. Post-assessment measures were filled out at home and mailed back to the Clinic by participants no more than 2 weeks after the intervention's completion.
4 secondary outcomes
Change in Symptom Checklist-90- Revised
Time frame: Baseline, Post-intervention (within 2 weeks after completion of 8-week intervention)
Change in Five-Factor Mindfulness Questionnaire (FFMQ)
Time frame: Baseline, Post-intervention (within 2 weeks after completion of 8-week intervention)
Change in Hamilton Anxiety & Depression Scale (HADS)
Time frame: Baseline, Post-intervention (within 2 weeks after completion of 8-week intervention)
Change in Tinnitus Visual Analogue Scale (VAS)
Time frame: Baseline, Post-intervention (within 2 weeks after completion of 8 week intervention)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Oct 2014.
- Background: PubMed 12238249Andersson G. Psychological aspects of tinnitus and the application of cognitive-behavioral therapy. Clin Psychol Rev. 2002 Sep;22(7):977-90. doi: 10.1016/s0272-7358(01)00124-6.
- Background: PubMed 17570961Grossman P, Tiefenthaler-Gilmer U, Raysz A, Kesper U. Mindfulness training as an intervention for fibromyalgia: evidence of postintervention and 3-year follow-up benefits in well-being. Psychother Psychosom. 2007;76(4):226-33. doi: 10.1159/000101501.
- BackgroundHenry, J. L., & Wilson, P. H. (2001). The psychological management of chronic tinnitus. Needham Heights, MA: Allyn & Bacon.
- Background: PubMed 1609875Kabat-Zinn J, Massion AO, Kristeller J, Peterson LG, Fletcher KE, Pbert L, Lenderking WR, Santorelli SF. Effectiveness of a meditation-based stress reduction program in the treatment of anxiety disorders. Am J Psychiatry. 1992 Jul;149(7):936-43. doi: 10.1176/ajp.149.7.936.
- Background: PubMed 3897551Kabat-Zinn J, Lipworth L, Burney R. The clinical use of mindfulness meditation for the self-regulation of chronic pain. J Behav Med. 1985 Jun;8(2):163-90. doi: 10.1007/BF00845519.
- Background: PubMed 9773769Kabat-Zinn J, Wheeler E, Light T, Skillings A, Scharf MJ, Cropley TG, Hosmer D, Bernhard JD. Influence of a mindfulness meditation-based stress reduction intervention on rates of skin clearing in patients with moderate to severe psoriasis undergoing phototherapy (UVB) and photochemotherapy (PUVA). Psychosom Med. 1998 Sep-Oct;60(5):625-32. doi: 10.1097/00006842-199809000-00020.
- Background: PubMed 11802836Mason O, Hargreaves I. A qualitative study of mindfulness-based cognitive therapy for depression. Br J Med Psychol. 2001 Jun;74 Part 2:197-212.
- Background: PubMed 10755808Moller AR. Similarities between severe tinnitus and chronic pain. J Am Acad Audiol. 2000 Mar;11(3):115-24.
- Background: PubMed 17907231Pradhan EK, Baumgarten M, Langenberg P, Handwerger B, Gilpin AK, Magyari T, Hochberg MC, Berman BM. Effect of Mindfulness-Based Stress Reduction in rheumatoid arthritis patients. Arthritis Rheum. 2007 Oct 15;57(7):1134-42. doi: 10.1002/art.23010.
- Background: PubMed 17451612Sadlier M, Stephens SD, Kennedy V. Tinnitus rehabilitation: a mindfulness meditation cognitive behavioural therapy approach. J Laryngol Otol. 2008 Jan;122(1):31-7. doi: 10.1017/S0022215107007438. Epub 2007 Apr 23.
- BackgroundSpeca, M., Carlson, L. E., Mackenzie, M. J., & Angen, M. (2006). Mindfulness-based stress reduction (MBSR) as an intervention for cancer patients. In R. A. Baer (Ed.), Mindfulness-based treatment approaches: Clinician's guide to evidence base and applications (pp. 239-261). San Diego, CA: Elsevier Academic Press.
- BackgroundSurawy C, Roberts J, Silver A. (2005). The effect of mindfulness training on mood and measures of fatigue, activity, and quality of life in patients with chronic fatigue syndrome on a hospital waiting list: a series of exploratory studies. Behavioural and Cognitive Psychotherapy; 33:103-09
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Jennifer Gans, PsyD study director
Clinical Psychologist
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Mindfulness Based Tinnitus Reduction in people with Tinnitus and Anxiety, run by University of California, San Francisco at 2 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 28 Oct 2014. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in Tinnitus Handicap Inventory (THI) (time frame: Baseline, Post-intervention (within 2 weeks after completion of 8-week intervention)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01229709, which also lists 15 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Oct 2014.