- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02293512
A Comparison of Three Psychoeducational Group Interventions for Veterans With Tinnitus
A Comparison of CBT and CET Interventions for Veterans With Tinnitus
Study Overview
Status
Conditions
Detailed Description
Tinnitus (i.e., ringing in the ears) is currently the most prevalent disability in the VA system. Numerous clinical interventions have been created to systematically address the range of issues caused by tinnitus. Only a few tinnitus interventions have focused on coping strategies. Coping strategies are cognitive, affective, and behavioral attempts to master new events, such as the onset of a disability or an impairment like tinnitus, that are overwhelming to an individual, and that because of their newness, an individual does not necessarily have automatic, adaptive responses. Evidence suggests that CET is effective in facilitating adaptive coping strategies among individuals with several types of impairments or disabilities. The proposed study will be the first application of CET to a tinnitus population.
The present study proposes a development of a CET protocol for tinnitus and a pilot study that assesses the effectiveness of the CET and ACT interventions compared to the current clinical practice of using a CBT intervention. All 3 psycho-educational interventions will be compared to a usual care group. The overarching goal of the proposed pilot study is to gain information that can be used to provide individuals with tinnitus with the best care for helping them to more successfully cope with tinnitus.
The aims of this research are to: 1) develop a CET protocol for tinnitus by means of information gathered from two focus groups and from CET consultants; 2) to examine whether a 3-session CET psycho-educational intervention is more effective than a 3-session CBT psycho-educational intervention or a 3-session ACT psycho-educational intervention, as compared to a usual care, in increasing coping strategies among individuals with tinnitus.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Oregon
-
Portland, Oregon, United States, 97239
- VA Portland Health Care System, Portland, OR
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Development Phase (Phase 1)-focus groups:
Inclusion criteria are the following (more details are provided below):
- 1) Veterans;
- 2) have chronic tinnitus that is sufficiently bothersome to warrant intervention-see below for explanation;
- 3) able to communicate in English;
- 4) willing and able to give written informed consent;
- 5) use hearing aids if needed; and
- 6) have participated in the PTM program at the VA Portland Healthcare System.
Testing Phase (Phase 2)-interventions:
Inclusion criteria are the following:
- 1) Veterans and civilians;
- 2) have a score of at least 25 on the Tinnitus Functional Index ([TFI]; Meikle, J.A. Henry, et al., 2012);
- 3) have two errors or less on a six-item cognitive screening instrument (Callahan, Unverzagt, Hui, Perkins, & Hendrie, 2002);
- 4) able to communicate in English;
- 5) willing and able to give written informed consent; and
- 6) use hearing aids if needed.
Exclusion Criteria:
Development Phase (Phase 1)-focus groups:
Exclusion criteria are:
- Not meeting inclusion criteria 1-6,
- nor have any other factor that would preclude full participation in the study.
Testing Phase (Phase 2)-interventions:
Exclusion criteria are:
- Not meeting inclusion criteria 1-6,
- having participated in the PTM program or Phase 1 of this study,
- or having any other factor that would preclude full participation in the study. Recruitment for Phase 2 will begin in year 1 once the CET protocol is finalized.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Coping Effectiveness Training
Coping Effectiveness Training (CET) is provided in a 3-session intervention to facilitate coping strategies among individuals with tinnitus.
The CET psychoeducational intervention teaches coping skills to increase understanding of stress and coping with tinnitus, and to help individuals better know how to match appropriate coping strategies, based on whether the stressful situation is changeable or not.
|
A CET psychoeducational intervention is provided to increase understanding of stress and coping with tinnitus, and to better learn how to match appropriate coping strategies, based on whether the stressful situation is changeable or not.
Other Names:
|
|
Active Comparator: Cognitive-behavioral therapy
Cognitive-behavioral therapy (CBT) is provided in a 3-session psychoeducational intervention to reduce negative affectivity triggered by tinnitus.
CBT treatments for tinnitus target the reduction of psychopathology by altering cognitive distortions, automatic thoughts, and core beliefs, as well as behavioral techniques to reduce physiological arousal.
|
CBT treatments for tinnitus target the reduction of psychopathology by altering cognitive distortions, automatic thoughts, and core beliefs, as well as behavioral techniques to reduce physiological arousal.
Other Names:
|
|
Active Comparator: Acceptance and Commitment Therapy
Acceptance and Commitment Therapy (ACT) is provided in a 3-session psychoeducational intervention to decrease resistance to tinnitus and increase committed action based on values, despite having tinnitus.
|
An ACT psycho-educational intervention to reduce distress and resistance about having tinnitus and to increase committed actions based on one's values.
Other Names:
|
|
No Intervention: Wait-list control group
Wait-list control group involves no intervention.
This is a 'usual care' group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Coping
Time Frame: Baseline
|
The Brief COPE scale (Carver, 1997) is a widely-used 28-item short form of the COPE Inventory (Carver, Scheier et al., 1989).
This instrument measures 14 coping subscales.
Each item is scored using a 1-4 frequency scale (i.e., 1= "I haven't been doing this it at all" to 4= "I've been doing this a lot"), where higher scores reflect greater use of the coping strategy.
A three-factor structure was used as follows: (a) Engagement coping (EC), including active coping, positive reframing, planning, accepting, and use of humor (items n = 12; score range 12-48); (b) disengagement coping (DC), including self-distancing, denial, behavioral disengagement, and self-blame (items n = 6; score range 6-24); and (c) social support coping (SS), including instrumenal support, emotional support, venting, and religion (items n = 8; score range 8-32).
|
Baseline
|
Collaborators and Investigators
Investigators
- Principal Investigator: Erin C Martz, PhD, VA Portland Health Care System, Portland, OR
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- C1578-P
- RX001578 (Other Grant/Funding Number: VA RR&D)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Tinnitus
-
State University of New York at BuffaloUniversity at BuffaloCompletedTinnitus, Subjective | Tinnitus | Noise Induced Tinnitus | Tinnitus, Objective | Tinnitus Aggravated | Tinnitus, Pulsatile | Tinnitus, Spontaneous Oto-Acoustic Emission | Tinnitus, Clicking | Tinnitus, Tensor Tympani InducedUnited States
-
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen UniversityRecruiting
-
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen UniversityNot yet recruiting
-
The First Affiliated Hospital with Nanjing Medical...Recruiting
-
TC Erciyes UniversityThe Scientific and Technological Research Council of TurkeyCompleted
-
University of Dublin, Trinity CollegeRecruitingBimodal Electrical-Sound Stimulation and Auditory Training for Chronic Tonal Tinnitus (NITESGON-ADT)Tinnitus, Subjective | Tinnitus | Chronic TinnitusIreland
-
Necmettin Erbakan UniversityActive, not recruitingSubjective Tinnitus | Neuromodulation | Chronic TinnitusTurkey (Türkiye)
-
Mohab MohammedNot yet recruitingPulsatile Tinnitus (Diagnosis)
-
Philipps University Marburg Medical CenterLinkoeping University; Eriksholm Research Centre; University Hospital of Gießen...CompletedTinnitus | Subjective Tinnitus | Chronic TinnitusGermany
-
Nicolas GninenkoRecruitingTinnitus, Subjective | Tinnitus, Bilateral | Tinnitus, Noise Induced | Tinnitus, Hearing Loss, Cochlear Implant UsersUnited States
Clinical Trials on Coping Effectiveness Training
-
National Human Genome Research Institute (NHGRI)CompletedAutism Spectrum DisordersUnited States
-
Karolinska InstitutetSwedish Red Cross University CollegeCompleted
-
University of California, San FranciscoNational Institute of Mental Health (NIMH)CompletedHIV InfectionsUnited States
-
Research Foundation for Mental Hygiene, Inc.Columbia UniversityWithdrawn
-
Oregon Health and Science UniversityUniversity of GeorgiaActive, not recruitingHIV SeropositivityUnited States
-
Ohio UniversityNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)Completed
-
Duke UniversityNational Heart, Lung, and Blood Institute (NHLBI); National Institutes of Health...CompletedCardiorespiratory FailureUnited States
-
Duke UniversityCompletedHematopoietic Neoplasms (Leukemia, Lymphoma, Multiple Myeloma)United States
-
Children's Hospital and Health System Foundation...University of Wisconsin, MadisonCompletedEpilepsy | Asthma | Spina Bifida | Rheumatologic Conditions (JRA,Lupus)United States
-
Ondokuz Mayıs UniversityNot yet recruitingStress Urinary IncontinenceTurkey